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SLOVENIA The Report referred to in Article 9 of Directive 2003/ 99/ EC TRENDS AND SOURCES OF ZOONOSES AND ZOONOTIC AGENTS IN HUMANS, FOODSTUFFS, ANIMALS AND FEEDINGSTUFFS including information on foodborne outbreaks, antimicrobial resistance in zoonotic agents and some pathogenic microbiological agents IN 2006

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Page 1: SLOVENIASlovenia VARS Competent authority Monitoring program preparing Collect data in animals, food and feed Epidemiological investigation National report preparing Contact point

SLOVENIA

The Report referred to in Article 9 of Directive 2003/ 99/ EC

TRENDS AND SOURCES OF ZOONOSES ANDZOONOTIC AGENTS IN HUMANS, FOODSTUFFS, ANIMALS ANDFEEDINGSTUFFS

including information on foodborne outbreaks, antimicrobialresistance in zoonotic agents and some pathogenicmicrobiological agents

IN 2006

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INFORMATION ON THE REPORTING AND MONITORING SYSTEMCountry: SloveniaReporting Year: 2006Institutions and laboratories involved in reporting and monitoring:Laboratory name Description ContributionHealthInspectorate of theRepublic ofSloveniaHIRS

Competent authority Monitoring program­preparingCollect data in foodEpidemiological investigation

Institute of PublicHealth of theRepublic ofSlovenia IPHRS

Researches Laboratory Monitoring program­preparing Collect data in humans Scientific advice and supportAnalysis and testing

NationalVeterinaryInstituteNVI

ResearchesLaboratory

Scientific advice and supportAnalysis and testing

VeterinaryAdministration ofthe Republic ofSloveniaVARS

Competent authority Monitoring program­preparingCollect data in animals, food and feedEpidemiological investigationNational report­preparingContact point with EC

Slovenia 2006 Report on trends and sources of zoonoses

Slovenia 2006

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PREFACEThis report is submitted to the European Commission in accordance with Article 9 of Council Directive 2003/ 99/ EC1. The information has also been forwarded to the European Food Safety Authority (EFSA). The report contains information on trends and sources of zoonoses and zoonotic agents in Slovenia during theyear 2006. The information covers the occurrence of these diseases and agents in humans, animals, foodstuffsand in some cases also in feedingstuffs. In addition the report includes data on antimicrobial resistance in somezoonotic agents and commensal bacteria as well as information on epidemiological investigations of foodborneoutbreaks. Complementary data on susceptible animal populations in the country is also given. The information given covers both zoonoses that are important for the public health in the whole EuropeanCommunity as well as zoonoses, which are relevant on the basis of the national epidemiological situation. The report describes the monitoring systems in place and the prevention and control strategies applied in thecountry. For some zoonoses this monitoring is based on legal requirements laid down by the CommunityLegislation, while for the other zoonoses national approaches are applied. The report presents the results of the examinations carried out in the reporting year. A national evaluation of theepidemiological situation, with special reference to trends and sources of zoonotic infections, is given.Whenever possible, the relevance of findings in foodstuffs and animals to zoonoses cases in humans isevaluated. The information covered by this report is used in the annual Community Summary Report on zoonoses that ispublished each year by EFSA.

­1 Directive 2003/ 99/ EC of the European Parliament and of the Council of 12 December 2003 on the monitoring ofzoonoses and zoonotic agents, amending Decision 90/ 424/ EEC and repealing Council Directive 92/ 117/ EEC, OJ L 325,17.11.2003, p. 31

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LIST OF CONTENTS1. ANIMAL POPULATIONS 12. INFORMATION ON SPECIFIC ZOONOSES AND ZOONOTIC AGENTS 32.1. SALMONELLOSIS 42.1.1. General evaluation of the national situation 42.1.2. Salmonellosis in humans 62.1.3. Salmonella in foodstuffs 222.1.4. Salmonella in animals 382.1.5. Salmonella in feedingstuffs 622.1.6. Salmonella serovars and phagetype distribution 672.1.7. Antimicrobial resistance in Salmonella isolates 722.2. CAMPYLOBACTERIOSIS 1642.2.1. General evaluation of the national situation 1642.2.2. Campylobacteriosis in humans 1652.2.3. Campylobacter in foodstuffs 1702.2.4. Campylobacter in animals 1782.2.5. Antimicrobial resistance in Campylobacter isolates 1812.3. LISTERIOSIS 1892.3.1. General evaluation of the national situation 1892.3.2. Listeriosis in humans 1902.3.3. Listeria in foodstuffs 1932.3.4. Listeria in animals 1972.4. E. COLI INFECTIONS 1982.4.1. General evaluation of the national situation 1982.4.2. E. Coli Infections in humans 1992.4.3. Escherichia coli, pathogenic in foodstuffs 2032.4.4. Escherichia coli, pathogenic in animals 2072.5. TUBERCULOSIS, MYCOBACTERIAL DISEASES 2102.5.1. General evaluation of the national situation 2102.5.2. Tuberculosis, Mycobacterial Diseases in humans 2112.5.3. Mycobacterium in animals 2152.6. BRUCELLOSIS 2192.6.1. General evaluation of the national situation 2192.6.2. Brucellosis in humans 2202.6.3. Brucella in foodstuffs 2222.6.4. Brucella in animals 2222.7. YERSINIOSIS 2312.7.1. General evaluation of the national situation 2312.7.2. Yersiniosis in humans 2322.7.3. Yersinia in foodstuffs 2362.7.4. Yersinia in animals 2392.8. TRICHINELLOSIS 2402.8.1. General evaluation of the national situation 2402.8.2. Trichinellosis in humans 2412.8.3. Trichinella in animals 245

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2.9. ECHINOCOCCOSIS 2532.9.1. General evaluation of the national situation 2532.9.2. Echinococcosis in humans 2542.9.3. Echinococcus in animals 2572.10. TOXOPLASMOSIS 2632.10.1. General evaluation of the national situation 2632.10.2. Toxoplasmosis in humans 2642.10.3. Toxoplasma in animals 2672.11. RABIES 2682.11.1. General evaluation of the national situation 2682.11.2. Rabies in humans 2702.11.3. Lyssavirus (rabies) in animals 2722.12. Q­FEVER 2742.12.1. General evaluation of the national situation 2742.12.2. Coxiella (Q­fever) in animals 274

3. INFORMATION ON SPECIFIC INDICATORS OF ANTIMICROBIALRESISTANCE

275

3.1. ESCHERICHIA COLI, NON­PATHOGENIC 2763.1.1. General evaluation of the national situation 2763.1.2. Antimicrobial resistance in Escherichia coli, non­pathogenic isolates 277

4. INFORMATION ON SPECIFIC MICROBIOLOGICAL AGENTS 2974.1. HISTAMINE 2984.1.1. General evaluation of the national situation 2984.1.2. Histamine in foodstuffs 2994.2. ENTEROBACTER SAKAZAKII 3014.2.1. General evaluation of the national situation 3014.2.2. Enterobacter sakazakii in foodstuffs 3024.3. STAPHYLOCOCCAL ENTEROTOXINS 3044.3.1. General evaluation of the national situation 3044.3.2. Staphylococcal enterotoxins in foodstuffs 305

5. FOODBORNE OUTBREAKS 306

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1. ANIMAL POPULATIONS

The relevance of the findings on zoonoses and zoonotic agents has to be related to the size and nature of theanimal population in the country.

A. Information on susceptible animal population

Sources of information:

Source:Livestock numbers and number of holdings: Statistical office of the Republic of SloveniaNumber of slaughtered animals: Veterinary Administration of the Republic of Slovenia

Dates the figures relate to and the content of the figures:

Reference date for year 2005 is 1 June 2005.Reference day for year 2006 is 1 December 2006.Livestock numbers and number of holdings: Reference date is the date the obtained data refer to. Number of slaughtered animals: The number of slaughtered animals in 2006.

Definitions used for different types of animals, herds, flocks and holdings as well as thetypes covered by the information:

Definitions and other explanationsAgricultural holding is a single unit, both organisational and operating, of agricultural area utilised,forests, buildings, equipment and labour force, which has a single management and which is engagedin agricultural production.

Additional information

METHODOLOGICAL EXPLANATIONSThe purpose of the surveyThe Farm Structure Survey (FSS) is one of the basic statistical surveys in the field of agriculture. Inaccordance with EU regulation it is conducted as a census every 10 years. Between censuses it can beconducted as a sample survey.Observation unitsObservation units are agricultural holdings satisfying the criteria of EU comparable threshold and allagricultural enterprises and co­operatives.Data on agricultural enterprises and co­operatives were collected by questionnaire by post.

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Table Susceptible animal populations

* Only if different than current reporting yearAnimal species Category of

animalsLivestock numbers(live animals)

Number ofslaughtered animals

Number of holdings Number of herds orflocks

Year* Year* Year* Year*Cattle (bovineanimals)

young cattle (1­2years)

120813 30628 2005

adult cattle over 2years

196604 37921 2005

calves (under 1year)

136617 33535 2005

in total 454033 140430 43675 2005Ducks in total 12535 2582 2005Gallus gallus(fowl)

broilers 1566749 24189983 4355 2005

laying hens 1119666 402881 43818 2005Geese in total 1904 868 2005Goats in total 27798 315 4108 2005Pigs breeding animals 53645 6151 2005

fattening pigs 241327 25886 2005in total 575116 428007 33945 2005

Sheep in total 131528 10224 5747 2005Solipeds, domestic horses ­ in total 19249 2005 1497 5128 2005

Turkeys in total 151589 2005 510631 1251 2005

Footnote

Source:Number of holdings, Livestock numbers: Statistical office of the Republic of SloveniaNumber of slaughtered animals: Veterinary Administration of the Republic of Slovenia

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2. INFORMATION ON SPECIFIC ZOONOSES AND ZOONOTICAGENTS

Zoonoses are diseases or infections, which are naturally transmissible directly or indirectly between animals andhumans. Foodstuffs serve often as vehicles of zoonotic infections. Zoonotic agents cover viruses, bacteria,fungi, parasites or other biological entities that are likely to cause zoonoses.

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2.1. SALMONELLOSIS

2.1.1. General evaluation of the national situation

A. General evaluation

History of the disease and/ or infection in the country

After the second World War only Salmonella Typhi and Paratyphi were notified. In 1950­sSalmonella Typhi and Paratyphi infections were more and more rare, other Salmonella serotypes weremore and more frequent. From 1946 to 1953 3414 cases of Salmonella Typhi and 3415 cases of Salmonella Paratyphi werenotified. Among them 180 patients with Salmonella Typhi and 41 patients with Salmonella Paratyphidied. After year 1953 epidemiological situation changed. More other Salmonella serotypes (SalmonellaTyphimurium, Choleraesuis, Enteritidis etc.) were identified and less Salmonella Typhi and Paratyphi.From the year 1954 to 2000 188 serotypes of Salmonella were identified and 82742 notifications ofSalmonella gastroenteritis in Slovenia. In last years Salmonella Enteritidis encounters more than 90% of Salmonella isolates in Slovenia.Salmonella Typhi, S.Paratyphi are notified only as imported infections.

National evaluation of the recent situation, the trends and sources of infection

The number of notified human Salmonella cases declined from 3307 notifications in 2004 to 1519 in2005 and 2006. The incidence of notified Salmonella cases dropped to 76 per 100 000 inhabitants. The average number of notified Salmonella cases in last 5 years in Slovenia was 2615 cases, thehighest number was in year 2003 ­ 4005 cases. Most frequent serotypes are: Salmonella Enteritidis, Salmonella Typhimurium, Salmonella Infantis.The real burden of Salmonella human infections is unknown, because we collate data only onnotificated cases.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

The incidence of human Salmonella infections in 2006 is the same as in year 2005 ­ according tonotificated number of Salmonella human cases. Source of infection are probably still poultry and eggs, but also bad hygiene and lack of knowledge ofmode of transmission or prevention of infection. PFGE analysisi of outbreaks helps us to identifysource of infection. (Phagetyping of Salmonella spp. is not yet implemented in Slovenia).The top­five serovars in veterinary laboratories in Slovenia were S. Enteritidis, S. Infantis, S.Typhimurium, S. Derby and S. Stanleyville. The scopes of other serovars, isolated from feed, animalsand food differ significantly from each other, indicating their different sources. It seems that thespread of these serovars from feed to animals and further to food is efficiently prevented in mostcases.Of 21 strains, isolated from animals and belonging to 18 different serovars, that are not considered tobe of public health importance nor the top­five in Slovenia (reported in detail in the tables), 4 strainsbelonging to 3 serovars (S. Tennesee, S. enterica susp. houtenae, serogoup C1) were resistant toStreptomycin, and 1 strain of S. Menden to Streptomycin and Spectinomycin, the remaining 16 were

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fully susceptible to all the 20 antimicrobials tested. Of the 6 strains, isolated in veterinary laboratories from food, belonging to 5 different serovars otherthan those of public health importance or the top­five in Slovenia (reported in detail in the tables),only the strain of S. Saintpaul was resistant to Streptomycin and Spectinomycin, while the remaining5 strains were fully susceptible to all the 20 antimicrobials tested. Except for the majority of strains of S. Typhimurium, some strains of S. Infantis and S. Derby and 1strain of S. Virchow, the majority of the isolated strains was fully susceptible to all the 20antimicrobials tested (including all but 2 S. Enteritidis strains), while only a few were resistant to justone antimicrobial (usually Streptomycin). So the situation regarding antimicrobial resistance inSalmonella is considered to be good. Regarding the results of susceptibility testing in E. coli, fromwhich resistance can be transferred to Salmonella, Monitoring should continue and the risk ofdevelopment of highly resistant strains should not be neglected.

Recent actions taken to control the zoonoses

New booklets with information about Salmonella in food for consumers.

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2.1.2. Salmonellosis in humans

A. Salmonellosis in humans

Reporting system in place for the human cases

Human cases are notifiable by national Law on Infectious Diseases (official Gazette number 69/ 95).Medical doctors, laboratories are obliged to notify cases on daily basis to local institutes of publichealth. Local institutes of public health notify disease to Institute of Public Health of R. Slovenia.Notification after the second World War.

Case definition

According to definitions of EU comission.

Diagnostic/ analytical methods used

Serologic and biochemical identification: isolation on SS agar and selen medium, serotypisation Oand H according to Kauffman White scheme. Laboratory of Institute of Public Health of Celje developed also PFGE method for Salmonella isolatesfrom whole Slovenia.

Notification system in place

Human cases are notifiable by national Law on infectious diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia. Notification after second World War.

History of the disease and/ or infection in the country

After the second World War only Salmonella Typhi and Paratyphi were notified. In 1950­sSalmonella Typhi and Paratyphi infections were more and more rare, other Salmonella serotypes weremore and more frequent. From 1946 to 1953 3414 cases of Salmonella Typhi and 3415 cases of Salmonella Paratyphi werenotified. Among them 180 patients with Salmonella Typhi and 41 patients with Salmonella Paratyphidied. After year 1953 epidemiological situation changed. More other Salmonella serotypes (SalmonellaTyphimurium, Choleraesuis, Enteritidis etc.) were identified and less Salmonella Typhi and Paratyphi.From the year 1954 to 2000 188 serotypes of Salmonella were identified and 82 742 notifications ofSalmonella gastroenteritis in Slovenia. In last years Salmonella Enteritidis encounters more than 90% of Salmonella isolates in Slovenia.Salmonella Typhi, S.Paratyphi are notified only as imported infections.

Results of the investigation

The number of notified human Salmonella cases declined from 3307 notifications in 2004 to 1519 in2005 and 2006. The incidence of notified Salmonella cases dropped to 76 per 100 000 inhabitants. (The average number of notified Salmonella cases in last 5 years in Slovenia was 2615 cases, thehighest number was in year 2003 ­ 4005 cases). Most frequent serotypes are: Salmonella Enteritidis, Salmonella Typhimurium, Salmonella Infantis,

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Salmonella Coeln.The real burden of Salmonella human infections is unknown, because we collate data on notificatedcases.

National evaluation of the recent situation, the trends and sources of infection

The incidence of human Salmonella infections has recently decreased according to notificated numberof Salmonella human cases. Source of infection are probably still poultry and eggs, but also badhygiene.

Relevance as zoonotic disease

Salmonella human infections are important as zoonotic disease. Salmonella is still most commonbacterial enteropathogen, Campylobacter is second most important.

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Table Salmonella in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.Unknown status

Salmonella

1519

75.75

00

00

1519

S. Abony

10.05

1

S. Agona

80.4

8

S. Anatum

10.05

1

S. Bispebjerg

10.05

1

S. Bovismorbificans

20.1

2

S. Braenderup

20.1

2

S. Brandenburg

10.05

1

S. Coeln

160.8

16

S. Derby

20.1

2

S. Enteritidis

1342

67.1

1342

S. Hadar

10.05

1

S. Heidelberg

20.1

2

S. Infantis

50.2

5

S. Kaapstad

10.05

1

S. Kentucky

20.1

2

S. Kottbus

10.05

1

S. Litchfield

10.05

1

S. Livingstone

20.1

2

S. M

bandaka

10.05

1

S. M

ontevideo

10.05

1

S. Napoli

20.1

2

S. New

port

10.05

1

S. Paratyphi B

130.6

13

S. Saintpaul

10.05

1

S. Schleissheim

20.1

2

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S. Senftenberg

10.05

1

S. Stanley

40.2

4

S. Stanleyville

50.2

5

S. Thompson

80.4

8

S. Typhi

30.1

3

S. Typhimurium

562.8

56

S. Virchow

10.05

1

S. Species

100.5

10

S. group B

140.7

14

S. group C

20.1

2

S. group D

20.1

2

S. group C2

10.05

1

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Table Salmonella in hum

ans ­ Age distribution (Part A

)

S. Abony

S. Agona

S. Anatum

S. Bispebjerg

S. Bovismorbificans

S. Braenderup

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

00

01

10

00

00

0

1 to 4 years

11

20

20

00

00

0

5 to 14 years

31

20

00

00

0

15 to 24 years

21

11

01

00

0

25 to 44 years

00

00

00

11

0

45 to 64 years

00

01

11

10

10

1

65 years and older

11

00

00

00

0

Age unknown

Total :

1 0

1 8

3 5

1 1

0 1

1 0

2 1

1 2

1 1

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Table Salmonella in hum

ans ­ Age distribution (Part B

)

S. Brandenburg

S. Coeln

S. Derby

S. Enteritidis

S. Hadar

S. Heidelberg

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

10

10

00

2612

140

00

1 to 4 years

32

11

10

177

9087

10

1

5 to 14 years

11

00

00

328

177

151

00

0

15 to 24 years

32

10

00

188

9296

11

00

0

25 to 44 years

21

11

10

298

151

147

10

1

45 to 64 years

11

64

20

00

199

98101

00

0

65 years and older

00

00

00

126

4779

00

0

Age unknown

Total :

1 1

0 16

10

6 2

2 0

1342

667

675

1 1

0 2

0 2

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Table Salmonella in hum

ans ­ Age distribution (Part C

)

S. In

fantis

S. Kaapstad

S. Kentucky

S. Kottbus

S. Litchfield

S. Livingstone

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

11

00

00

11

00

0

1 to 4 years

00

00

00

10

10

00

5 to 14 years

11

00

00

00

0

15 to 24 years

00

00

00

00

0

25 to 44 years

32

11

12

20

10

1

45 to 64 years

00

00

00

00

0

65 years and older

00

00

00

11

0

Age unknown

Total :

5 4

1 1

0 1

2 2

0 1

1 0

1 0

1 2

1 1

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Table Salmonella in hum

ans ­ Age distribution (Part D

)

S. M

bandaka

S. M

ontevideo

S. Napoli

S. New

port

S. Paratyphi B

S. Saintpaul

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

00

01

01

1 to 4 years

11

05

32

5 to 14 years

00

03

21

15 to 24 years

11

00

00

00

25 to 44 years

00

01

01

21

1

45 to 64 years

11

00

02

20

11

65 years and older

11

00

00

Age unknown

Total :

1 0

1 1

1 0

2 2

0 1

0 1

13

8 5

1 0

1

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Table Salmonella in hum

ans ­ Age distribution (Part E

)

S. Schleissheim

S. Senftenberg

S. Stanley

S. Stanleyville

S. Thompson

S. Typhi

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

00

00

00

10

11

10

00

0

1 to 4 years

00

00

00

00

00

00

00

0

5 to 14 years

00

00

00

11

01

01

00

0

15 to 24 years

00

00

00

00

01

10

10

1

25 to 44 years

20

22

11

11

04

22

11

0

45 to 64 years

00

00

00

10

11

10

11

0

65 years and older

00

01

12

02

11

00

00

00

0

Age unknown

Total :

2 0

2 1

0 1

4 1

3 5

3 2

8 5

3 3

2 1

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Table Salmonella in hum

ans ­ Age distribution (Part F

)

S. Typhimurium

S. Virchow

Salmonella sp

p.S. group B

S. group C

S. group D

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

00

01

01

10

10

00

00

0

1 to 4 years

1411

32

11

52

30

00

00

0

5 to 14 years

96

32

11

10

10

00

11

0

15 to 24 years

76

11

10

11

00

00

00

0

25 to 44 years

106

40

00

20

21

10

00

0

45 to 64 years

51

41

13

21

31

20

00

11

0

65 years and older

113

81

01

11

01

10

00

0

Age unknown

00

0

Total :

56

33

23

1 1

0 10

5 5

14

5 9

2 2

0 2

2 0

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Table Salmonella in hum

ans ­ Age distribution (Part G

) S. group C2

Age Distribution

All

MF

<1 year

11

1 to 4 years

5 to 14 years

15 to 24 years

25 to 44 years

45 to 64 years

65 years and older

Age unknown

Total :

1 1

0

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Table Salmonella in hum

ans ­ Seasonal distribution (Part A

)

S. Abony

S. Agona

S. Anatum

S. Bispebjerg

S.Bovismorbificans

S. Braenderup

S. Brandenburg

S. Coeln

Month

Cases

Cases

Cases

Cases

Cases

Cases

Cases

Cases

January

0 2

0 0

0 0

February

0 2

0 0

0 0

March

0 2

0 0

1 0

April

0 0

0 0

0 0

May

0 1

0 1

0 1

June

0 0

0 0

0 3

July

0 1

0 0

0 1

August

1 0

1 1

1 0

4

Septem

ber

0 0

0 1

0 0

2

October

0 0

0 0

0 5

Novem

ber

0 0

0 0

0 0

Decem

ber

0 0

0 0

0 0

not known

Total :

1 8

1 1

2 1

1 16

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Table Salmonella in hum

ans ­ Seasonal distribution (Part B

)

S. Derby

S. Enteritidis

S. Hadar

S. Heidelberg

S. In

fantis

S. Kaapstad

S. Kentucky

S. Kottbus

Month

Cases

Cases

Cases

Cases

Cases

Cases

Cases

Cases

January

35

February

38

March

32

April

50

1

May

215

1 1

June

219

1 1

July

151

1 2

August

201

1

Septem

ber

2 151

1 1

1

October

111

Novem

ber

75

Decem

ber

64

not known

Total :

2 1342

1 2

5 1

2 1

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Table Salmonella in hum

ans ­ Seasonal distribution (Part C

)

S. Litchfield

S. Livingstone

S. M

bandaka

S. M

ontevideo

S. Napoli

S. New

port

S. Paratyphi B

S. Saintpaul

Month

Cases

Cases

Cases

Cases

Cases

Cases

Cases

Cases

January

0 0

February

0 0

March

0 0

April

0 1

0 1

May

1 0

June

0 1

1 0

July

0 1

1

August

0 1

0

Septem

ber

0 4

October

0 1

4

Novem

ber

0 4

Decem

ber

0 0

not known

Total :

1 1

1 1

2 1

13

1

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Table Salmonella in hum

ans ­ Seasonal distribution (Part D

)

S. Schleissheim

S. Senftenberg

S. Stanley

S. Stanleyville

S. Thompson

S. Typhi

S. Typhimurium

S. Virchow

Month

Cases

Cases

Cases

Cases

Cases

Cases

Cases

Cases

January

2 1

February

2

March

1

April

1 2

May

5

June

1 2

July

5 1

5

August

1 1

1 1

9

Septem

ber

2 2

2 10

October

10

Novem

ber

2 7

1

Decem

ber

1 2

not known

Total :

2 1

4 5

8 3

56

1

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Table Salmonella in hum

ans ­ Seasonal distribution (Part E

)

Salmonella sp

p.

S. group B

S. group C

S. group D

S. group C2

Month

Cases

Cases

Cases

Cases

Cases

January

1 0

0 0

February

0 1

0 0

March

1 1

0 0

April

0 1

0 0

May

1 1

0 0

June

0 3

0 1

July

1 3

0 1

August

2 0

0 0

Septem

ber

0 3

1 0

October

1 1

0 0

1

Novem

ber

1 0

0 0

Decem

ber

2 0

1 0

not known

Total :

10

14

2 2

1

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2.1.3. Salmonella in foodstuffs

A. Salmonella spp. in eggs and egg products

Monitoring system

Sampling strategy

HIRSMonitoring ­ eggs at retailAnnual monitoring programme was prepared with respect to the results of programme/ controlscarried out in the previous year, epidemiological situation.The majority of samples were taken in cities with 10000 inhabitants or more and number ofsamples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over the situation.Sampling carried out by health inspectors.Programme: 100 samples of table eggs.

Frequency of the sampling

Eggs at egg packing centres (foodstuff based approach)

Sampling distributed evenly throughout the year

Eggs at retail

Sampling takes place during the months January ­ October

Egg products (at production plant and at retail)

Other: none

Type of specimen taken

Eggs at egg packing centres (foodstuff based approach)

Other: /

Eggs at retail

Surface of egg shell

Egg products (at production plant and at retail)

Other: /

Methods of sampling (description of sampling techniques)

Eggs at retail

A sample ­ a package of 10 eggs is stored in a sterile bag or other sterile container.Samples must be delivered to the laboratory in the shortest time possible. The period of

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time elapsing from sampling to analysis shall by no means exceed 24 hours. Thetemperature during storage and transport should not exceed + 4 oC.

Definition of positive finding

Eggs at retail

A sample from which Salmonella has been isolated.

Diagnostic/ analytical methods used

Eggs at retail

Bacteriological method: ISO 6579:2002

Egg products (at production plant and at retail)

Other: /

Preventive measures in place

GHP, GHM,HACCP

Measures in case of the positive findings

Necessary enforcement actions were taken.

Notification system in place

Whenever zoonotic agent­Salmonella is detected in samples taken, relevant authorities must beinformed.

Results of the investigation

HIRSMonitoring at retailWithin the monitoring programme 100 samples were taken. Two samples were positive on presenceof Salmonella Enteritidis, 1 sample was positive on presence of Salmonella Typhimurium.

B. Salmonella spp. in broiler meat and products thereof

Monitoring system

Sampling strategy

At slaughterhouse and cutting plant

VARSPoultry meat sampling is carried out in all the registered slaughterhouses and/ orcutting plants. Samples were taken at cutting plants operating within 4 major poultry slaughterhousesand in all other (low capacity) slaughterhouses.Sampling is carried out by the official veterinarians.

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At retail

HIRSAnnual monitoring programme was prepared with respect to the results of programme/ controls carried out in the previous year, epidemiological situation, CommissionRecommendation concerning a coordinated programme for the official control offoodstuffs.The majority of samples were taken in cities with 10000 inhabitants or more andnumber of samples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over thesituation.Sampling carried out by health inspectors.Programme: 100 samples of fresh meat per annum.

Frequency of the sampling

At slaughterhouse and cutting plant

Other: At cutting plants operating within 4 major poultry slaughterhouses, 1 randomsample is taken once a week, normally 75% of broiler meat and 25% of turkey meat.At low capacity slaughterhouses, 1 random sample is taken once a month.

At retail

Sampling takes place during the months February ­ October

Type of specimen taken

At slaughterhouse and cutting plant

Fresh meat

At retail

Fresh meat

Methods of sampling (description of sampling techniques)

At slaughterhouse and cutting plant

A meat sample weighing approximately 300g is removed by a sterile instrument, andin poultry, the thoracic section is removed and stored in a sterile bag.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

At retail

A sample weighing minimum 300 g is stored in a sterile bag or other sterile container.Samples must be delivered to the laboratory in the shortest time possible. The period oftime elapsing from sampling to analysis shall by no means exceed 24 hours. The

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temperature during storage and transport should not exceed + 4 oC.

Definition of positive finding

At slaughterhouse and cutting plant

Meat: sample shall be considered positive where the causative agent has been isolatedfrom the sample.

At retail

A sample from which Salmonella has been isolated.

Diagnostic/ analytical methods used

At slaughterhouse and cutting plant

Bacteriological method: ISO 6579:2002

At retail

Bacteriological method: ISO 6579:2002

Preventive measures in place

GMP, GHP, HACCPAt the moment food business operators introduce the system of additional labelling of poultry meatwhich includes special warning to the customers to treat poultry meat at requested temperature beforeany use.

Measures in case of the positive findings or single cases

HIRSMonitoring at retail:Additional sampling was carried out and other necessary enforcement actions. Since product was nolonger on the market at the time of receiving analytical results of samples taken at the retail level in allcases in house control was required.

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.Business operator must notify VARS of the presence of Salmonellae in the establishment.HIRSWhenever zoonotic agent­Salmonella is detected in samples taken, relevant authorities must beinformed.

Results of the investigation

VARSSampling in cutting plants.In 2006, 172 broiler meat samples were taken. Salmonella was not detected in the meat.

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HIRSMonitoring in retail:Within the monitoring programme 100 samples of prepacked meat were taken. Salmonella was notdetected in any sample.

National evaluation of the recent situation, the trends and sources of infection

Situation concerning Salmonella spp. in the fresh meat in production remains favourable also in 2006.

C. Salmonella spp. in turkey meat and products thereof

Monitoring system

Sampling strategy

At slaughterhouse and cutting plant

VARSPoultry meat sampling is carried out in all the registered slaughterhouses and/ orcutting plants. Samples were taken at cutting plants operating within 4 major poultry slaughterhousesand in all other (low capacity) slaughterhouses.Sampling is carried out by the official veterinarians.

At retail

/

Frequency of the sampling

At slaughterhouse and cutting plant

Other: At cutting plants operating within 4 major poultry slaughterhouses, 1 randomsample is taken once a week, normally 75% of broiler meat, and 25% of turkey meat.At low capacity poultry slaughterhouses, 1 random sample is taken once a month.

At retail

Other: /

Type of specimen taken

At slaughterhouse and cutting plant

Fresh meat

At retail

Other: /

Methods of sampling (description of sampling techniques)

At slaughterhouse and cutting plant

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A meat sample weighing approximately 300g is removed by a sterile instrument, andin poultry, the thoracic section is removed and stored in a sterile bag.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

At retail

/

Definition of positive finding

At slaughterhouse and cutting plant

Meat: sample shall be considered positive where the causative agent has been isolatedfrom the sample.

At retail

/

Diagnostic/ analytical methods used

At slaughterhouse and cutting plant

Bacteriological method: ISO 6579:2002

At retail

Other: /

Preventive measures in place

GMP, GHP, HACCP

Measures in case of the positive findings or single cases

/

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.Business operator must notify VARS of the presence of Salmonellae in the establishment.

Results of the investigation

In 2006, 56 turkey meat samples were taken. Salmonella was not detected in the meat.

National evaluation of the recent situation, the trends and sources of infection

Situation concerning Salmonella spp. in the fresh meat in production remains favourable also in 2006.On the basis of results obtained in production, the meat of domestic animals does not pose a threat to

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public health.

D. Salmonella spp. in pig meat and products thereof

Monitoring system

Sampling strategy

At slaughterhouse and cutting plant

VARSPorcine meat sampling is carried out in all the registered high capacity cutting plants.Sampling of the surface of porcine carcasses at slaughterhouses.

At retail

/

Frequency of the sampling

At slaughterhouse and cutting plant

Other: In the bovine and porcine meat cutting plants, 1 meat sample is taken every 2months. Every year, 50 samples of porcine carcass surface are taken atslaughterhouses.

At retail

Other: /

Type of specimen taken

At slaughterhouse and cutting plant

Other: Fresh meat, Carcass surface swab

At retail

Other: /

Methods of sampling (description of sampling techniques)

At slaughterhouse and cutting plant

A meat sample weighing approximately 300g is removed by a sterile instrument, andin poultry, the thoracic section is removed and stored in a sterile bag.A carcass surface sample is taken with one sterile swab from the surface of 3x100 cm2.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

At retail

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/

Definition of positive finding

At slaughterhouse and cutting plant

Positive sample is a sample, where the zoonotic agent has been isolated from.Isolation of agent in 25g or in the swab taken.

At retail

/

Diagnostic/ analytical methods used

At slaughterhouse and cutting plant

Bacteriological method: ISO 6579:2002

At retail

Other: /

Preventive measures in place

GMP, GHP, HACCP

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of establishments subjected to veterinary controls­ Identification of animal products and their traceability­ Veterinary controls in establishments

Measures in case of the positive findings or single cases

/

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.Business operator must notify VARS f the presence of Salmonellae in the establishment.

Results of the investigation

Sampling in cutting plants.In 2006, 159 porcine meat samples were taken. Salmonella was not detected in the meat.In 2006, 35 samples of porcine carcass surface were taken. Salmonella was not detected.

National evaluation of the recent situation, the trends and sources of infection

Situation concerning Salmonella spp. in the fresh meat in production remains favourable also in 2006.

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On the basis of results obtained in production, the meat of domestic animals does not pose a threat topublic health.

E. Salmonella spp. in bovine meat and products thereof

Monitoring system

Sampling strategy

At slaughterhouse and cutting plant

VARSBovine meat sampling is carried out in all the registered high capacity cutting plants. Sampling of the surface of bovine carcasses at slaughterhouses.

Frequency of the sampling

At slaughterhouse and cutting plant

Other: In the bovine and porcine meat cutting plants, 1 meat sample is taken every 2months. Every year, 50 samples of bovine carcass surface are taken at slaughterhouses.

Type of specimen taken

At slaughterhouse and cutting plant

Other: Fresh meat, Carcass swab

Methods of sampling (description of sampling techniques)

At slaughterhouse and cutting plant

A meat sample weighing approximately 300g is removed by a sterile instrument, andin poultry, the thoracic section is removed and stored in a sterile bag.A carcass surface sample is taken with one sterile swab from the surface of 3x100 cm2.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

Definition of positive finding

At slaughterhouse and cutting plant

Positive sample is a sample, where the zoonotic agent has been isolated from.Isolation of agent in 25g or in the swab taken.

Diagnostic/ analytical methods used

At slaughterhouse and cutting plant

Bacteriological method: ISO 6579:2002

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Preventive measures in place

GMP, GHP, HACCP

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.Business operator must notify VARS of the presence of Salmonellae in the establishment.

Results of the investigation

Sampling in cutting plants.In 2006, 155 bovine meat samples were taken. Salmonella was not detected in the meat.In 2006, 44 samples of bovine carcass surface were taken. Salmonella was not detected.

National evaluation of the recent situation, the trends and sources of infection

Situation concerning Salmonella spp. in the fresh meat in production remains favourable also in 2005.On the basis of results obtained in production, the meat of domestic animals does not pose a threat topublic health.

F. Salmonella spp. in food

Monitoring system

Sampling strategy

HIRS Monitoring at retailAnnual monitoring programme was prepared with respect to the results of programme/ controlscarried out in the previous year, epidemiological situation, legilsative criteria.The majority of samples were taken in cities with 10000 inhabitants or more and number ofsamples taken was proportional with the population in the region.They were taken at the retail level where sampling could give an overview over the situation.Sampling carried out by health inspectors.Programme:Eggs: 100 samples/ year;Minced meat (from bovine animals and/ or bigs): 100 samples/ year;Meat from broilers(meat preparation): 100 samples/ year;Molluschan shellfish: 30 samples/ year;Sprouted seeds: 30 samples/ year;Infant formula (dried): 30 samples/ year;Spices and herbs: 30 samples/ year;Fruits: 40 samples/ year;Vegetables: 80 samples/ year;Confectionary products and pastries: 250 samples/ year;Other processed foods products and prepared dishes (deli dishes, pates, sandwiches, etc.): 560 samples/ year;Milk and dairy products: 240 samples/ year;

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Other food of non animal origin: 30 samples/ year

Frequency of the sampling

Sampling takes place during the months January ­ December.

Methods of sampling (description of sampling techniques)

A sample weighing 300­400 g is removed by sterile instrument and stored in a sterile bag orother sterile container in a case the sample is not prepacked. In case of prepacked food,sufficient number of units is taken. Samples must be delivered to the laboratory in the shortesttime possible. The period of time elapsing from sampling to analysis shall by no means exceed24 hours. The temperature during storage and transport should not exceed + 4 oC.

Definition of positive finding

A sample from which Salmonella has been isolated.

Diagnostic/ analytical methods used

Bacteriological method: ISO 6579:2002; Cor.2004

Preventive measures in place

GMP, GHP, HACCP

Measures in case of the positive findings or single cases

Additional sampling was carried out and other necessary enforcement actions, including sending toRASFF where necessary.

Notification system in place

Whenever zoonotic agent­Salmonella is detected in samples taken, relevant authorities must beinformed.

Results of the investigation

HIRSMonitoring at retailIn 2006 among all 1620 samples taken at restaurants, retail and catering Salmonella was detected in 8samples (5 samples of minced meat (n=100) and 3 samples of eggs (n= 100)). Out of all 1620 samples taken, 0,5 % were positive on presence of Salmonella spp..

National evaluation of the recent situation, the trends and sources of infection

Situation concerning Salmonella spp. in food in retail is favourable.

G. Salmonella spp. in food ­ Meat from bovine animals and pig

Monitoring system

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Sampling strategy

HIRSMonitoring at retailAnnual monitoring programme was prepared with respect to the results of programme/ controlscarried out in the previous year, epidemiological situation.The majority of samples were taken in cities with 10000 inhabitants or more and number ofsamples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over the situation.Sampling carried out by health inspectors.Programme: 100 samples of minced meat (pig and/ or bovine) per annum.

Frequency of the sampling

Sampling takes place during the months from February to October.

Methods of sampling (description of sampling techniques)

A sample of prepacked minced meat weighing 300­400 g is stored in cooled container. Samplesmust be delivered to the laboratory in the shortest time possible. The period of time elapsingfrom sampling to analysis shall by no means exceed 24 hours. The temperature during storageand transport should not exceed + 4 oC.

Definition of positive finding

A sample from which Salmonella has been isolated.

Diagnostic/ analytical methods used

Bacteriological method: ISO 6579:2002; Cor. 2004

Preventive measures in place

GMP, GHM, HACCP

Measures in case of the positive findings or single cases

Additional sampling was carried out and other necessary enforcement actions.

Notification system in place

Whenever zoonotic agent­Salmonella is detected in samples taken, relevant authorities must beinformed.

Results of the investigation

HIRSMonitoring at retailIn 2006 out of 100 samples of minced meat taken, 5 samples were positive on presence of Salmonellaspp. (3 samples were positive on presence of Salmonella Typhimurium, 1 sample was positive onpresence of Salmonella Saintpaul and 1 was detected only as Salmonella spp.)

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Table Salmonella in poultry meat and products thereof

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

Meat from broilers (Gallusgallus)

­ ­ ­

fresh (1) ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 25g 172 0

meat preparation ­ ­ ­intended to be eaten cooked(2)

­ HIRS single 25g 100 0

Meat from turkey ­ ­ ­fresh ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 25g 56 0

(1) : (2) : prepacked

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Table Salmonella in milk and dairy products

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

Cheeses made from cows' milk ­soft and semi­soft ­ HIRS single 25g 30 0 0 0 0

Dairy products (excludingcheeses)

­ ­ ­

ice­cream ­ HIRS single 25g 200 0 0 0 0

sour milk ­ HIRS single 25g 10 0 0 0 0

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Table Salmonella in red meat and products thereof

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

S. Saintpaul

Meat from pig ­ ­ ­fresh (1) ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 25g 159 0

carcass ­ ­ ­­ at slaughterhouse ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single swab 35 0

Meat from bovine animals ­ ­ ­fresh (2) ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 25g 155 0

carcass ­ ­ ­­ at slaughterhouse ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single swab 44 0

Meat, red meat (meat frombovines, pigs, goats, sheep,horses, donkeys, bison andwater buffalos)

­ ­ ­

minced meat ­ ­ ­­ at retail ­ Monitoring ­ HIRS single 25g 100 5 0 3 1 1

(1) : (2) :

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Table Salmonella in other food

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

Eggs ­ ­ ­table eggs ­ ­ ­­ at retail ­ HIRS single egg shell 100 3 2 1

Molluscan shellfish ­cooked ­ HIRS single 25g 10 0 0 0 0

raw ­ HIRS single 25g 20 0 0 0 0

Sprouted seeds ­non­ready­to­eat ­ HIRS single 25g 30 0 0 0 0

Infant formula ­ ­ ­dried ­ ­ ­intended for infants below 6months

­ HIRS single 25g 30 0 0 0 0

Spices and herbs ­ ­ ­dried ­ ­ ­­ at retail ­ HIRS single 25g 30 0 0 0 0

Other processed food productsand prepared dishes

­ HIRS single 25g 560 0 0 0 0

Fruits ­ ­ ­non­precut ­ ­ ­frozen ­ HIRS single 25g 20 0 0 0 0

pre­cut ­ HIRS single 25g 20 0 0 0 0

Vegetables ­ ­ ­non­precut ­ HIRS single 25g 80 0 0 0 0

Confectionery products andpastes

­ HIRS single 25g 250 0 0 0 0

Other food of non­animalorigin

­ ­ ­

(powdered food exceptpowdered milk)

­ HIRS single 25g 30 0 0 0 0

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2.1.4. Salmonella in animals

A. Salmonella spp. in Gallus gallus ­ breeding flocks for egg production and flocksof laying hens

Monitoring system

Sampling strategy

Breeding flocks (separate elite, grand parent and parent flocks whennecessary)

VARSSampling shall be carried out in all breeding flocks including at least 250 birds.Animal owner or holder of activity of the hatchery shall at his own expense takesamples for analysis in order to detect the presence of Salmonella. Sampling shall becarried out at poultry breeding holdings or in hatcheries. Every eight weeks thesampling carried out by the holder of activity in the adult breeding flocks shall besubstituted by the official sampling, carried out by the official veterinarians.

Laying hens flocks

VARSSampling shall be carried out in all the flocks at holdings keeping laying hens, whichinclude more than 350 birds. Animal owner or holder of activity of the holding keepinglaying hens, shall at his own expence take samples for analysis in order to detect thepresence of Salmonella.

Frequency of the sampling

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Every flock is sampled

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Other: At four weeks of age and two weeks prior to entering the laying phase.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Every two weeks

Laying hens: Day­old chicks

Every flock is sampled

Laying hens: Rearing period

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Other: Two weeks prior to entering the laying phase.

Laying hens: Production period

Every fifteen weeks

Type of specimen taken

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Other: Internal linings of delivery boxes and dead chicks.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Other: Pooled faeces samples.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Other: Pooled faeces samples or pooled meconium samples or samples of dead chicks.

Laying hens: Day­old chicks

Other: Internal linings of delivery boxes and dead chicks.

Laying hens: Rearing period

Other: Pooled faeces samples.

Laying hens: Production period

Other: Pooled faeces samples

Methods of sampling (description of sampling techniques)

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Sampling of the internal linings of the boxes in which the chicks have been deliveredto the holding, and of the carcasses of the chicks found dead on arrival.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Pooled faeces samples made up of separate samples of fresh faeces each weighing notless than 1g taken at random from a number of sites in the building in which the birdsare kept, or, where the birds have free access to more than one building on a particularholding, from each group of buildings on the holding in which the birds are kept.

Breeding flocks: Production period

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In accordance with Annex III of Council Directive 92/ 117/ EEC.

Laying hens: Day­old chicks

Sampling of the internal linings of the boxes in which the chicks have been deliveredto the holding, and of the carcasses of the chicks found dead on arrival.

Laying hens: Rearing period

Pooled faeces samples made up of separate samples of fresh faeces each weighing notless than 1g taken at random from a number of sites in the building in which the birdsare kept, or, where the birds have free access to more than one building on a particularholding, from each group of buildings on the holding in which the birds are kept.

Laying hens: Production period

Pooled faeces samples made up of separate samples of fresh faeces each weighing notless than 1g taken at random from a number of sites in the building in which the birdsare kept, or, where the birds have free access to more than one building on a particularholding, from each group of buildings on the holding in which the birds are kept.

Case definition

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Laying hens: Day­old chicks

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Laying hens: Rearing period

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Laying hens: Production period

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Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Diagnostic/ analytical methods used

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004 ; Modified ISO 6579: 2002 (Recommendation by the CRL)

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Laying hens: Day­old chicks

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Laying hens: Rearing period

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Laying hens: Production period

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Vaccination policy

Breeding flocks (separate elite, grand parent and parent flocks when necessary)

Vaccination of breeding flocks is voluntary.

Other preventive measures than vaccination in place

Breeding flocks (separate elite, grand parent and parent flocks when necessary)

Persons, who in carrying out a registered activity of breeding or production come into directcontact with animals, foodstuffs, raw materials, products or waste, must have thoroughknowledge in contagious animal diseases, the prevention thereof and transmissibility to man,and in the regulations governing the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene in

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primary production ­ GAP, GHP, and record keeping.

Laying hens flocks

Persons, who in carrying out a registered activity of breeding or production come into directcontact with animals, foodstuffs, raw materials, products or waste, must have thoroughknowledge in contagious animal diseases, the prevention thereof and transmissibility to man,and in the regulations governing the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GAP, GHP, and record keeping.

Control program/ mechanisms

The control program/ strategies in place

Breeding flocks (separate elite, grand parent and parent flocks whennecessary)

National control programme in 2006 has been carried out in accordance with thenational legislation, on the basis of the Rules on the monitoring of zoonoses andzoonotic agents in poultry breeding flocks (transposing Council Directive 92/ 117/ EEC), and the Instructions on measures for the detection, prevention and suppressionof salmonellosis. The control mechanisms envisages inter alia as follows: ­ Registration and/ or approval of holdings, establishments, transporters, collectioncentres and dealers, who are subjected to veterinary checks ­ Identified flocks­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming fromholdings with an unverified or suspect epizootiological situation.

Laying hens flocks

National control programme is carried out in accordance with the national legislation,on the basis of the Instructions on measures for the detection, prevention andsuppression of salmonellosis. The control mechanisms envisages inter alia as follows: ­ Registration and/ or approval of holdings, establishments, transporters, collectioncentres and dealers, who are subjected to veterinary checks ­ Identified flocks­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming fromholdings with an unverified or suspect epizootiological situation

Measures in case of the positive findings or single cases

Breeding flocks (separate elite, grand parent and parent flocks when necessary)

The following measures shall be instituted in the suspect holding immediately after the business

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operator has reported the presence of Salmonella:­ Banning the movements and alienation of animals from the suspect flock;­ Banning the issuing of health certificates for animals from the suspect flock;­ Banning the trade in and circulation of eggs from the suspect flock;­ Banning the hatching of eggs from the suspect flock;­ Banning the slaughter of animals from the suspect flock;­ In case of larger flocks, restricting the movements of persons coming into contact withanimals from the suspect flock;­ Testing of animal feed kept at the holding for the presence of Salmonellae;­ Epizootiological investigation.Measures instituted shall remain in force until the presence of serovars Salmonella Enteritidis,Salmonella Typhimurium, Salmonella Hadar, Salmonella Virchow and Salmonella Infantis hasofficially been ruled out on the basis of confirmatory analysis results.On having confirmed the presence of serovars Salmonella Enteritidis, SalmonellaTyphimurium, Salmonella Hadar, Salmonella Virchow and Salmonella Infantis, the businessoperator shall, based on the internal monitoring and control plan, provide for theimplementation of the following measures:1. no bird from the flock, in which Salmonella has been detected, shall be moved from theholding, unless for slaughter to the slaughterhouse or for killing and destruction under officialveterinary control, where:­ slaughter shall be carried out at the slaughterhouse as the last batch in the slaughtering processof that particular production day, by a method minimising the possibility of spreadingSalmonella, and in accordance with the food hygiene law;­ products obtained from such poultry may be placed on the market or put into circulation ifthey have been subjected to processing guaranteeing the elimination of Salmonella, or theyshall be removed and used in accordance with the regulations governing the handling of animalby­products; the entire procedure shall be carried out under the control of official veterinarian;­ killing and destruction shall be carried out in accordance with the regulations governing thehandling of animal by­products;2. eggs laid by hens from positive flock shall be:­ delivered under official veterinary control to an approved establishment for the productionand/ or processing of egg products, where they shall be subjected to processing guaranteeingthe elimination of Salmonella. Eggs to be delivered to an establishment for the production and/ or processing of egg products shall be wrapped and packaged prior to shipment in a waypreventing the removal of individual eggs from the package. Packages must be identified by anote: PRODUCT FROM A POSITIVE FLOCK – COMPULSORY PRESCRIBEDPROCESSING; or­ destroyed on the spot, or processed in accordance with the regulations governing the handlingof animal by­products; 3. all eggs from positive flocks that are non­incubated at the hatchery shall be destroyed orprocessed in accordance with the regulations governing the handling of animal by­products;4. killing and destruction of day­old chicks from the positive flock;5. on removal and/ or dispatch of the flock, in which Salmonella has been detected, the manureand bedding shall be removed in accordance with the regulations governing the handling ofanimal by­products, followed by thorough cleaning and disinfection;6. prior to repopulation, bacteriological control of the efficiency of cleaning and disinfectionshall be carried out, with negative results.

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Laying hens flocks

The following measures shall be instituted in the suspect holding immediately after the businessoperator has reported the presence of Salmonella:­ Banning the movements and alienation of animals from the suspect flock;­ Banning the issuing of health certificates for animals from the suspect flock;­ Banning the trade in and circulation of eggs from the suspect flock;­ Banning the slaughter of animals from the suspect flock;­ In case of larger flocks, restricting the movements of persons coming into contact withanimals from the suspect flock;­ Testing of animal feed kept at the holding for the presence of Salmonellae;­ Epizootiological investigation.Measures instituted shall remain in force until the presence of serovars Salmonella Enteritidis,Salmonella Typhimurium, Salmonella Hadar, Salmonella Virchow and Salmonella Infantis hasofficially been ruled out on the basis of confirmatory analysis results.On having confirmed the presence of serovars Salmonella Enteritidis, SalmonellaTyphimurium, Salmonella Hadar, Salmonella Virchow and Salmonella Infantis, the businessoperator shall, based on the internal monitoring and control plan, provide for theimplementation of the following measures:1. no bird from the flock, in which Salmonella has been detected, shall be moved from theholding, unless for slaughter to the slaughterhouse or for killing and destruction under officialveterinary control, where:­ slaughter shall be carried out at the slaughterhouse as the last batch in the slaughtering processof that particular production day, by a method minimising the possibility of spreadingSalmonella, and in accordance with the food hygiene law;­ products obtained from such poultry may be placed on the market or put into circulation ifthey have been subjected to processing guaranteeing the elimination of Salmonella, or theyshall be removed and used in accordance with the regulations governing the handling of animalby­products; the entire procedure shall be carried out under the control of official veterinarian;­ killing and destruction shall be carried out in accordance with the regulations governing thehandling of animal by­products;2. eggs laid by hens from positive flock shall be:­ delivered under official veterinary control to an approved establishment for the productionand/ or processing of egg products, where they shall be subjected to processing guaranteeingthe elimination of Salmonella. Eggs to be delivered to an establishment for the production and/ or processing of egg products shall be wrapped and packaged prior to shipment in a waypreventing the removal of individual eggs from the package. Packages must be identified by anote: PRODUCT FROM A POSITIVE FLOCK – COMPULSORY PRESCRIBEDPROCESSING; or­ destroyed on the spot, or processed in accordance with the regulations governing the handlingof animal by­products; 5. on removal and/ or dispatch of the flock, in which Salmonella has been detected, the manureand bedding shall be removed in accordance with the regulations governing the handling ofanimal by­products, followed by thorough cleaning and disinfection;6. prior to repopulation, bacteriological control of the efficiency of cleaning and disinfectionshall be carried out, with negative results.

Notification system in place

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Breeding flock: In case that by monitoring the presence of Salmonella in a breeding flock is detected,the holder of the flock must officially notify VARS of the results. The laboratory must submit thediagnostic test results to the Main Office of VARS. This method of reporting must be carried out inaccordance with the provisions of the Rules on the monitoring of zoonoses and zoonotic agents inpoultry breeding flocks (transposing Council Directive 92/ 117/ EEC) since 2004, and prior to thatdate, the method of reporting diseases was used as prescribed in the Rules on contagious animaldiseases. Laying hens: In case that by monitoring the presence of Salmonella in a laying flock is detected, theholder of the flock must officially notify VARS of the results. The laboratory must submit thediagnostic test results to the Main Office of VARS.In case of presence of salmonellosis, or signs by which it may be suspected that an animal has becomesick with or died of Salmonella infection, the animal keeper shall immediately notify thereof theveterinary organisation, and the latter shall notify thereof the relevant VARS Regional Office.The authorised laboratory submits the diagnostic test results to the relevant Regional Office of VARS,and to the consigner of samples.Once a month and no later than the 20th day in the month, the authorised laboratories and RegionalOffices of VARS must report on the diagnostic test results to the Office for Contagious AnimalDiseases within VARS. This method of reporting is carried out in accordance with the provisions of the Rules on contagiousanimal diseases (applicable since 2002), and the reporting as such has been compulsory since 1996.

Results of the investigation

BREEDING FLOCKS – animals intended for the production of hatching eggsIn 2006, 6 laying hen parent flocks were tested – on the hatching egg line, and thereof, 1 grand­parentflocks and 5 parent flocks. Salmonella was not detected. LAYING HEN FLOCKS ­ animals intended for the production of table eggsIn 2006, 205 flocks were tested, and thereof, 40 flocks during rearing period and 165 adult flocks atproduction stage. Salmonella was not identified in flocks during rearing period whilst there were 3positive flocks at production stage, which amounts to 1.6 % of all flocks tested.

National evaluation of the recent situation, the trends and sources of infection

BREEDING FLOCKS – animals intended for the production of hatching eggsPresent situation in parent flocks intended for production of table eggs is rather favourable, as in 2006,Salmonella was not detected in any flock, while in 2005, two flocks were found positive during theproduction phase, and S. Enteritidis was isolated in both the cases.LAYING HEN FLOCKS ­ animals intended for the production of table eggsSituation in the laying hen flocks has been more favourable this year as well. One flock of laying hensin rearing period and 7 flocks of laying hens in production period were found positive in 2005, and in2006, only 3 flocks of laying hens in production period were found positive. Salmonella prevalence inflocks of laying hens thus decreased from 6,2 % in 2005 to 1,46 % in 2006.

Additional information

Business operator of breeding flocks for egg production may decide for flock treatment on the basis ofan antibiogram. If serovars Salmonella Enteritidis or Salmonella Typhimurium are detected in the breeding flocksbefore the onset of the laying phase, the business operator may decide for flock treatment on the basis

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of an antibiogram. Flock treatment may be carried out also in case of presence of Salmonella Hadar,Salmonella Virchow and Salmonella Infantis, irrespective of the age of the flock. In case of flock treatment, the business operator shall, based on the internal monitoring and controlplan, provide for the implementation of the following measures:­ no bird from the flock, in which Salmonella has been detected, shall be moved from the holding;­ transferring of the flock under treatment to a cleaned and disinfected facility within the holding; incase that the business operator has no spare facilities for such transferring of the flock, he shall carryout measures for sanitising the premises and ensuring the conditions of hygiene in the premises.Samples from the environment in the premises shall be taken for Salmonella testing;­ eggs intended for hatching shall be disinfected by a bactericidal gas immediately upon collection;­ specific and customised treatment – cleaning and disinfection of premises, installations, packagingmaterial in the hatchery;­ intensified microbiological controls in the hatchery ­ swabbing;­ specific and customised disinfection of eggs in the hatchery, in the disinfection room, and of eggsduring incubation;­ hatched poultry shall, as long as still damp in the incubator, be sanitised by a bactericidal gas;­ unhatched eggs, hatched deformed poultry and other animal by­products must be removed inaccordance with the regulations governing animal by­products;­ specific and customised cleaning and disinfection of the means of transport intended for carryingeggs and poultry;­ on completion of treatment, sampling of fresh faeces and/ or animals; first sampling shall take placeon day 5 after completion of treatment, or on expiry of the withdrawal period if exceeding five days;second sampling shall take place on completion of treatment, or on expiry of a double withdrawalperiod if exceeding five days.Measures instituted may be lifted in case of negative results of bacteriological tests of the first andsecond sampling.

B. Salmonella spp. in Gallus gallus ­ breeding flocks for meat production andbroiler flocks

Monitoring system

Sampling strategy

Breeding flocks (separate elite, grand parent and parent flocks whennecessary)

VARSSampling shall be carried out in all breeding flocks including at least 250 birds.Animal owner or holder of activity of the hatchery shall at his own expense takesamples for analysis in order to detect the presence of Salmonella. Sampling shall becarried out at poultry breeding holdings or in hatcheries. Every eight weeks thesampling carried out by the holder of activity in the adult breeding flocks shall besubstituted by the official sampling, carried out by the official veterinarians.

Broiler flocks

VARS

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Sampling shall be carried out in all the holdings rearing poultry for production –broilers. Animal owner or holder of activity of the holding keeping broilers, shall at hisown expence take samples for analysis in order to detect the presence of Salmonella.

Frequency of the sampling

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Every flock is sampled

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Other: At four weeks of age and two weeks prior to entering the laying phase.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Every two weeks

Broiler flocks: Before slaughter at farm

one to three weeks prior to slaughter

Type of specimen taken

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Other: Internal linings of delivery boxes and dead chicks.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Other: Pooled faeces samples.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Other: Pooled faeces samples.

Broiler flocks: Before slaughter at farm

Other: Pooled faeces sample and boot swabs.

Methods of sampling (description of sampling techniques)

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Sampling of the internal linings of the boxes in which the chicks have been deliveredto the holding, and of the carcasses of the chicks found dead on arrival.

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Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Pooled faeces samples made up of separate samples of fresh faeces each weighing notless than 1g taken at random from a number of sites in the building in which the birdsare kept, or, where the birds have free access to more than one building on a particularholding, from each group of buildings on the holding in which the birds are kept.

Breeding flocks: Production period

Pooled faeces samples made up of separate samples of fresh faeces each weighing notless than 1g taken at random from a number of sites in the building in which the birdsare kept, or, where the birds have free access to more than one building on a particularholding, from each group of buildings on the holding in which the birds are kept.

Broiler flocks: Before slaughter at farm

Pooled faeces samples made up of separate samples of fresh faeces each weighing notless than 1g taken at random from a number of sites (depending on number of birds inthe building) in the building in which the birds are kept, or, where the birds have freeaccess to more than one building on a particular holding, from each group of buildingson the holding in which the birds are kept.

Case definition

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Flock shall be considered positive where the causative agent has been identified in theconfirmatory sample of the official sampling.

Broiler flocks: Day­old chicks

Flock shall be considered positive where the causative agent has been identified in thesampling.

Broiler flocks: Before slaughter at farm

Flock shall be considered positive where the causative agent has been identified in thesampling.

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Diagnostic/ analytical methods used

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Day­old chicks

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Rearing period

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Breeding flocks (separate elite, grand parent and parent flocks whennecessary): Production period

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Broiler flocks: Before slaughter at farm

Other: Bacteriological method: Method in accordance with the OIE Manual, 5th ed.,2004; Modified ISO 6579: 2002 (Recommendation by the CRL)

Vaccination policy

Breeding flocks (separate elite, grand parent and parent flocks when necessary)

Vaccination of breeding flocks is voluntary.

Other preventive measures than vaccination in place

Broiler flocks

Persons, who in carrying out a registered activity of breeding or production come into directcontact with animals, foodstuffs, raw materials, products or waste, must have thoroughknowledge in contagious animal diseases, the prevention thereof and transmissibility to man,and in the regulations governing the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GAP, GHP, and record keeping.

Control program/ mechanisms

The control program/ strategies in place

Breeding flocks (separate elite, grand parent and parent flocks whennecessary)

National control programme is carried out in accordance with the national legislation,on the basis of the Rules on the monitoring of zoonoses and zoonotic agents in poultrybreeding flocks (transposing Council Directive 92/ 117/ EEC), and the Instructions on

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measures for the detection, prevention and suppression of salmonellosis. The control mechanisms envisages inter alia as follows: ­ Registration and/ or approval of holdings, establishments, transporters, collectioncentres and dealers, who are subjected to veterinary checks ­ Identified flocks­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming fromholdings with an unverified or suspect epizootiological situation.

Broiler flocks

National control programme is carried out in accordance with the national legislation,on the basis of the Instructions on measures for the detection, prevention andsuppression of salmonellosis. The control mechanisms envisages inter alia as follows: ­ Registration and/ or approval of holdings, establishments, transporters, collectioncentres and dealers, who are subjected to veterinary checks ­ Identified flocks­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming fromholdings with an unverified or suspect epizootiological situation.

Measures in case of the positive findings or single cases

Breeding flocks (separate elite, grand parent and parent flocks when necessary):Day­old chicks

See Breeding flocks for egg production.

Breeding flocks (separate elite, grand parent and parent flocks when necessary):Rearing period

See Breeding flocks for egg production.

Breeding flocks (separate elite, grand parent and parent flocks when necessary):Production period

See Breeding flocks for egg production.

Broiler flocks: Before slaughter at farm

On having identified the presence of serovars Salmonella Enteritidis, Salmonella Typhimurium,the business operator shall, based on the internal monitoring and control plan, provide for theimplementation of the following measures:1. no bird from the flock, in which Salmonella has been detected, shall be moved from theholding, unless for slaughter to the slaughterhouse or for killing and destruction under officialveterinary control, where:­ slaughter shall be carried out at the slaughterhouse as the last batch in the slaughtering process

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of that particular production day, by a method minimising the possibility of spreadingSalmonella, and in accordance with the food hygiene law;­ products obtained from such poultry may be placed on the market or put into circulation ifthey have been subjected to processing guaranteeing the elimination of Salmonella, or theyshall be removed and used in accordance with the regulations governing the handling of animalby­products; the entire procedure shall be carried out under the control of official veterinarian;2. on removal and/ or dispatch of the flock, in which Salmonella has been detected, the manureand bedding shall be removed in accordance with the regulations governing the handling ofanimal by­products, followed by thorough cleaning and disinfection;3. prior to repopulation, bacteriological control of the efficiency of cleaning and disinfectionshall be carried out, with negative results.

Notification system in place

Breeding flocks: In case that by monitoring the presence of Salmonella in a breeding flock is detected,the holder of the flock must officially notify VARS of the results. The laboratory must submit thediagnostic test results to the Main Office of VARS. This method of reporting must be carried out inaccordance with the provisions of the Rules on the monitoring of zoonoses and zoonotic agents inpoultry breeding flocks (transposing Council Directive 92/ 117/ EEC) since 2004, and prior to thatdate, the method of reporting diseases was used as prescribed in the Rules on contagious animaldiseases. Broiler flocks: The certificate on the state of health of broilers dispatched for slaughter shall, in caseof positive flocks, include a note “Salmonellae identified in the flock” and an indication of theappropriate serovar.In case of presence of salmonellosis, or signs by which it may be suspected that an animal has becomesick with or died of Salmonella infection, the animal keeper shall immediately notify thereof theveterinary organisation, and the latter shall notify thereof the relevant VARS Regional Office. The authorised laboratory submits the diagnostic test results to the relevant Regional Office of VARS,and to the consigner of samples.Once a month and no later than the 20th day in the month, the authorised laboratories and RegionalOffices of VARS must report on the diagnostic test results to the Office for Contagious AnimalDiseases within VARS. This method of reporting is carried out in accordance with the provisions of the Rules on contagiousanimal diseases (applicable since 2002), and the reporting as such has been compulsory since 1996.

Results of the investigation

BREEDING FLOCKS – animals intended for the production of hatching eggsIn 2006, 60 laying hen parent flocks were tested – on the meat line, and thereof, 1 grand­parent flockand 59 parent flocks. Salmonella was not identified.BROILERS (chicks for fattening) ­ animals intended for meat productionIn 2006, Salmonella was detected in 9 flocks of 1.748 flocks during rearing period tested, amountingto 0.51 %. In six flocks the presence of S. enteritidis was confirmed, in two flocks S. Kisii and in oneflock S.Tennessee.

National evaluation of the recent situation, the trends and sources of infection

BREEDING FLOCKS ­ animals intended for the production of hatching eggsPresent situation in parent flocks intended for meat production is rather favourable, as in 2006,

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Salmonella was not detected in any flock, while in 2005, one adult flock was found positive duringthe production phase, and S. Enteritidis was isolated.BROILERS ­ animals intended for meat productionThe situation in broiler flocks did not vary significantly in 2006 as compared to 2005. Percentage ofall positive flocks in 2006 is a bit lower (0,51), but the percentage of flocks in which S. Enteritidiswas detected (0,34) remains rather similar to that of 2005.

C. Salmonella spp. in pigs

Monitoring system

Sampling strategy

Breeding herds

VARSDisease is monitored on the basis of clinical signs and/ or detection of salmonellosis inother animals in the same holding.

Multiplying herds

See Fattening herds

Fattening herds

VARSSampling is carried out continually throughout the year at all the registered porcineslaughter establishments, taking into account sample distribution with regard to rearingestablishments. Sampled are animals raised in the Republic of Slovenia only.A slaughter animal constitutes an epidemiological unit.Sampling is carried out by the slaughterhouse official veterinarians.Also see Breeding heards

Frequency of the sampling

Fattening herds at slaughterhouse (herd based approach)

Other: At slaughter establishments, 1 animal – 1 sample is sampled every month

Type of specimen taken

Fattening herds at slaughterhouse (herd based approach)

Other: 1 sample – 5 or more lymph nodes from the ileocaecal region

Methods of sampling (description of sampling techniques)

Breeding herds

Immediately upon suspicion of disease on the basis of clinical signs and/ or detectionof salmonellosis in other animals in the same holding, the authorised veterinaryorganisation must submit for investigation the dead animal carcasses, rectal swabs of

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suspect animals, samples of litter and feed.

Multiplying herds

See Breeding herds

Fattening herds at farm

See Breeding herds

Fattening herds at slaughterhouse (herd based approach)

Lymph nodes sampled are removed by a sterile instrument and stored in a sterile bag.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

Case definition

Breeding herds

The disease shall be considered officially confirmed on the basis of the clinical signs and/ orpositive bacteriological test results; in the opposite case it shall be considered that the diseasehas been ruled out.

Multiplying herds

See Breeding herds

Fattening herds at farm

See Breeding herds

Fattening herds at slaughterhouse (herd based approach)

Positive animal means an animal, where a positive sample has been taken from. Positive samplemeans a sample, where the zoonotic agent has been isolated from.

Diagnostic/ analytical methods used

Breeding herds

Other: Bacteriological method: Method according to the OIE Manual, 5th ed., 2004, for lymphnodes the method recomended by CRL­Salmonella.

Multiplying herds

Other: Bacteriological method: Method according to the OIE Manual, 5th ed., 2004, for lymphnodes the method recomended by CRL­Salmonella.

Fattening herds at farm

Other: Bacteriological method: Method according to the OIE Manual, 5th ed., 2004, for lymph

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nodes the method recomended by CRL­Salmonella.

Fattening herds at slaughterhouse (herd based approach)

Other: Bacteriological method: ISO 6579: 2002, for lymph nodes the method recomended byCRL­Salmonella.

Other preventive measures than vaccination in place

Breeding herds

Persons, who in carrying out a registered activity of breeding or production come into directcontact with animals, foodstuffs, raw materials, products or waste, must have thoroughknowledge in contagious animal diseases, the prevention thereof and transmissibility to man,and in the regulations governing the protection against contagious diseases. In accordance withlegislation, the business operator shall provide for conditions of hygiene in primary production­ GAP, GHP, and record keeping.

Multiplying herds

See Breeding herds

Fattening herds

See Breeding herds

Control program/ mechanisms

The control program/ strategies in place

Breeding herds

National control programme is carried out in accordance with the national legislation,on the basis of the Instructions on measures for the detection,prevention andsuppression of salmonellosis. The control programme envisages inter alia as follows:­ Immediate confirmation of the disease in case of suspected presence by takingsamples for the diagnostic purposes, epizootiological investigation, and institutingappropriate measures immediately upon suspecting the presence of disease at thesuspect holding. Measures shall be instituted as long as the suspicion of disease has notofficially been ruled out.­ Instituting of supplementary measures in the infected holding.­ Registration and/ or approval of holdings, establishments, transporters, collectioncentres and dealers, who are subjected to veterinary checks ­ Identified and registrated animals ­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming fromholdings with an unverified or suspect epizootiological situation.

Multiplying herds

See Breeding herds

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Fattening herds

See Breeding herds

Measures in case of the positive findings or single cases

On the official confirmation of disease, the following measures shall be instituted at the holding inaddition to those instituted at the suspected presence of disease:­ disinfection of incoming raw materials to constitute animal feed;­ treatment of infected animals with an appropriate antibiotic or chemotherapeutic agent on the basisof antibiogram;­ DDD measures;­ other measures for sanitising the infected holding

Notification system in place

Official notification of monitoring results.In case of presence of salmonellosis, or signs by which it may be suspected that an animal has becomesick with or died of Salmonella infection, the animal keeper shall immediately notify thereof theveterinary organisation, and the latter shall notify thereof the relevant VARS Regional Office,submitting also monthly reports on the developments concerning the disease.

Results of the investigation

In 2006, samples of ileocaecal lymph nodes of 224 porcine animals were taken. Salmonella wasdetected in 5 samples (2,23%), where S. typhimurium was identified three times and S. Enteritidis andS.spp. once.

National evaluation of the recent situation, the trends and sources of infection

As compared to 2005 (5,37 % of positives), the number of positive cases in 2006 decreased by morethan one half (2,23 % positives), and thus we find the situation concerning Salmonella in porcineanimals rather favourable.

D. Salmonella spp. in bovine animals

Monitoring system

Sampling strategy

VARSSampling is carried out continually throughout the year at all the registered bovine slaughterestablishments, taking into account sample distribution with regard to rearing establishments.Sampled are animals raised in the Republic of Slovenia only.A slaughter animal constitutes an epidemiological unit.Sampling is carried out by the slaughterhouse official veterinarians.Pasive monitoring in calvesDisease is monitored on the basis of clinical signs and/ or detection of salmonellosis in otheranimals in the same holding.

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Frequency of the sampling

Animals at slaughter (herd based approach)

Other: At slaughter establishments, 1 animal – 1 sample is sampled every month.

Type of specimen taken

Animals at slaughter (herd based approach)

Faeces

Methods of sampling (description of sampling techniques)

Animals at farm

Immediately upon suspicion of disease on the basis of clinical signs and/ or detectionof salmonellosis in other animals in the same holding, the authorised veterinaryorganisation must submit for investigation the dead animal carcasses, rectal swabs ofsuspect animals, samples of litter and feed.

Animals at slaughter (herd based approach)

Faeces are sampled prior to slaughter, and after slaughter, following the evisceration,the intestinal wall is aseptically opened and the intestinal content removed from theintestines and stored in a sterile plastic bag.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

Case definition

Animals at farm

The disease shall be considered officially confirmed on the basis of the clinical signsand/ or positive bacteriological test results; in the opposite case it shall be consideredthat the disease has been ruled out.

Animals at slaughter (herd based approach)

Positive animal means an animal, where a positive sample has been taken from.Positive sample means a sample, where the zoonotic agent has been isolated from.

Diagnostic/ analytical methods used

Animals at slaughter (herd based approach)

Bacteriological method: Modified by ISO 6579: 2002

Other preventive measures than vaccination in place

Persons, who in carrying out a registered activity of breeding or production come into direct contact

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with animals, foodstuffs, raw materials, products or waste, must have thorough knowledge incontagious animal diseases, the prevention thereof and transmissibility to man, and in the regulationsgoverning the protection against contagious diseases. In accordance with legislation, the businessoperator shall provide for conditions of hygiene in primary production ­ GAP, GHP, and recordkeeping.

Control program/ mechanisms

The control program/ strategies in place

National control programme is carried out in accordance with the national legislation, on thebasis of the Instructions on measures for the detection, prevention and suppression ofsalmonellosis. The control programme envisages inter alia as follows:­ Immediate confirmation of the disease in case of suspected presence by taking samples for thediagnostic purposes, epizootiological investigation, and instituting appropriate measuresimmediately upon suspecting the presence of disease at the suspect holding. Measures shall beinstituted as long as the suspicion of disease has not officially been ruled out.­ Instituting of supplementary measures in the infected holding.­ Registration and/ or approval of holdings, establishments, transporters, collection centres anddealers, who are subjected to veterinary checks ­ Identified and registrated animals ­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming from holdings withan unverified or suspect epizootiological situation.

Measures in case of the positive findings or single cases

Measures in case of the positive findings or single cases:On the official confirmation of disease, the following measures shall be instituted at the holding inaddition to those instituted at the suspected presence of disease:­ disinfection of incoming raw materials to constitute animal feed;­ treatment of infected animals with an appropriate antibiotic or chemotherapeutic agent on the basisof antibiogram;­ DDD measures;­ other measures for sanitising the infected holding

Notification system in place

Official notification of monitoring results.In case of presence of salmonellosis, or signs by which it may be suspected that an animal has becomesick with or died of Salmonella infection, the animal keeper shall immediately notify thereof theveterinary organisation, and the latter shall notify thereof the relevant VARS Regional Office,submitting also monthly reports on the developments concerning the disease.

Results of the investigation

In 2006, 236 faeces samples were taken. Salmonella was detected in three samples (1,27%), whereonce S.Infantis, once S.Brancaster and once S.Kottbus were identified.

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Table Salmonella in breeding flocks of Gallus gallus

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

Gallus gallus (fowl) ­ ­ ­grandparent breeding flocksfor egg production line (1)

­ VARS flock 1 0

parent breeding flocks for eggproduction line

­

during rearing period ­ VARS flock 2 0

during production period ­ VARS flock 3 0

grandparent breeding flocksfor meat production line (2)

­ VARS flock 1 0

parent breeding flocks formeat production line

­

day­old chicks ­ VARS flock 11 0

during rearing period ­ VARS flock 20 0

during production period ­ VARS flock 28 0

(1) : during production period(2) : during production period

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Table Salmonella in other poultry

­­

Source of information

Sampling unit

Units tested

Total units positive for Salmonella spp.

S. Enteritidis

S. Typhimurium

Salmonella spp., unspecified

S. Tennessee

S. Kisii

S. Havana

S. Infantis

S. Heidelberg

Gallus gallus (fowl)

­­­

laying hens

­during rearing period

­VARS

flock

400

during production period

­VARS

flock

165

31

01

00

10

0

broilers

­day­old chicks

­VARS

flock

520

during rearing period

­VARS

flock

1748

96

00

12

00

0

Turkeys

­meat production flocks

­day­old chicks

­VARS

flock

122

00

00

00

11

during rearing period

­VARS

flock

802

00

00

00

20

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Table Salmonella in other birds

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

Pigeons ­ single

Ostriches ­ single

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Table Salmonella in other animals

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

S. Brancaster

S. In

fantis

S. Kottbus

Cattle (bovine animals) ­­ at slaughterhouse ­ animalsample ­ faeces ­ Monitoring ­official sampling

­ VARS animal 236 3 0 0 0 1 1 1

Pigs ­fattening pigs ­­ at slaughterhouse ­ animalsample ­ lymph nodes ­Monitoring ­ officialsampling

­ VARS animal 224 5 1 3 1 0 0 0

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2.1.5. Salmonella in feedingstuffs

A. Salmonella spp. in feed

History of the disease and/ or infection in the country

VARSIn Slovenia feed was surveilled for the presence of Salmonella for decades. The prevalence was ratherlow and the isolated strains were generally the most susceptible to antimicrobials of all the strainstested. Many serovars were isolated only from feed and were not found later in the chain:feed­animal­food.

National evaluation of the recent situation, the trends and sources of infection

The recent situation reflects the efforts of controling Salmonella in feed and is considered good.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Of 4 strains isolated from feed, belonging to 4 different serovars (S. Enteritidis, S. Schwarzengrund,S. Havana and S. Worthington), only S. Enteritidis and S. Schwarzengrund were tested forantimicrobial resistance and in S. Enteritidis resistance to Streptomycin was detected.(Subjected to antimicrobial resistant testing were strains isolated from all samples tested in theNational veterinary institute laboratory).

Recent actions taken to control the zoonoses

FeedinstuffsMonitoring system:­ sampling strategy: target sampling (in accordance with the Programme of feed control in 2006)­ frequency of the sampling: domestic feed material of plant and animal origin, imported feed materialof plant and animal origin, process control of feed in trade ­ preventative measures: own controls by holders of activity (HACCP)­ control programme: Program of feed control in 2006, in accordance with Article 7(2) and Article78(4) of the Veterinary Compliance Criteria Act (VCCA; UL RS 93/ 05), and Article 33(a) of AnimalFeed Act (UL RS 97/ 04), and Articles 41, 43 and 45(2a) of the Regulation(EC)No.882/ 2004(OJ L165/ 04) ­ measures in case of positive findings: in accordance with Article 4(2) and Article 8(5) of the Ruleson feed safety criteria (UL RS 101/ 06)­ notification system in place: RASFF system and mutual notification between the competentauthorities in the sector of food safety, in accordance with Decree coordinating the operation ofministries and agencies within them that are competent for food safety at inclusion into the riskanalysis process (UL RS 56/ 03).

Additional information

Feedinstuffs­ frequency of the sampling: domestic feed material of plant and animal origin (80 samples), importedfeed material of plant and animal origin (10 samples), process control in feed mills (120 samples),

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controls of feed in trade (140 samples)­ description of sampling techniques: in accordance with the Rules of the official methods of samplingfor the monitoring and inspection and control of animal feed, additives and premixes (UL RS 41/ 03)­ definition of positive finding: analysis result (1 = positive, 0 = negative)­ analytical methods used: ISO/ FDIS 6579:2002 SOP 221

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Table Salmonella in feed material of animal origin

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Enteritidis

S. Typhimurium

Salmonella sp

p., unspecified

Feed material of land animalorigin

­ ­ ­

dairy products ­ VARS batch 25g 3 0

Feed material of marineanimal origin

­ ­ ­

fish meal ­ VARS batch 25g 3 0

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Table Salmonella in other feed matter

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Typhimurium

S. Enteritidis

Salmonella sp

p., unspecified

Feed material of cereal grainorigin

­ ­ ­

other cereal grain derived ­ VARS batch 25g 4 0

Feed material of oil seed orfruit origin

­ ­ ­

sunflower seed derived ­ VARS batch 25g 2 0

other oil seeds derived ­ VARS batch 25g 17 0

Other feed material ­ ­ ­tubers, roots and similarproducts

­ VARS batch 25g 4 0

other seeds and fruits ­ VARS batch 25g 4 0

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Table Salmonella in compound feedingstuffs

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Salmonella sp

p.

S. Typhimurium

S. Enteritidis

Salmonella sp

p., unspecified

S. Havana

S. W

orthington

Compound feedingstuffs forcattle

­ ­ ­

final product ­ VARS batch 25g 61 1 0 0 0 1

Compound feedingstuffs forpigs

­ ­ ­

final product ­ VARS batch 25g 83 0

Compound feedingstuffs forpoultry (non specified)

­ ­ ­

final product ­ VARS batch 25g 104 1 0 0 0 1

Pet food ­ ­ ­dog snacks (pig ears, chewingbones)

­ VARS batch 25g 2 0

Compound feedingstuffs forfish

­ VARS batch 25g 4 0

Compound feedingstuffs forrabbits

­ VARS batch 25g 7 0

Compound feedingstuffs, notspecified

­ VARS batch 25g 18 0

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2.1.6. Salmonella serovars and phagetype distribution

The methods of collecting, isolating and testing of the Salmonella isolates are described in the chapters aboverespectively for each animal species, foodstuffs and humans. The serotype and phagetype distributions can beused to investigate the sources of the Salmonella infections in humans. Findings of same serovars andphagetypes in human cases and in foodstuffs or animals may indicate that the food category or animal species inquestion serves as a source of human infections. However as information is not available from all potentialsources of infections, conclusions have to be drawn with caution.

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Table Salmonella serovars in animals

Serovars

Cattle (bovine animals)

Pigs

Gallus gallus (fowl)

Other poultry

Pigeons

Mice

Reptiles

Turkeys

Ostriches

Swans

Snakes

Moose

Sources of isolates (*)

MC

MC

MC

MC

MC

MC

MC

MC

MC

MC

MC

MC

Num

ber of isolates in the laboratory

N=

Num

ber of isolates serotyped

N=

31

51

413

00

10

10

11

10

01

01

04

03

­ Num

ber of isolates per type

S. Agona

1

S. Amsterdam

1

S. Brancaster

1

S. Coeln

1

S. Derby

3

S. Enteritidis

119

11

11

S. Gabon

1

S. Havana

1

S. Heidelberg

3

S. Infantis

11

5

S. Kedougou

1

S. Kisii

1

S. Kottbus

1

S. M

enden

1

S. New

port

1

S. Ohio

1

S. Oranienburg

1

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S. Paratyphi B

11

S. Stanleyville

13

S. Tennessee

1

S. Typhimurium

31

S. Virchow

1

S. W

orthington

1

Salmonella sp

p.

1

S. group O:7

11

S. enterica subsp. houtenae

1

S. enterica subsp. salamae

1

Footnote

(*) M

: Monitoring, C : Clinical

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Table Salmonella serovars in food

Serovars

Meat from bovine animals

Meat from pig

Meat from broilers (Gallus gallus)

Other poultry

Other products of animal origin

Meat from bovine animals and pig

Meat from turkey

Meat from broilers (Gallus gallus) ­ offal

Meat from turkey ­ offal

Meat from pig ­ offal

Sources of isolates (*)

MC

MC

MC

MC

MC

MC

MC

MC

MC

MC

Num

ber of isolates in the laboratory

N=

Num

ber of isolates serotyped

N=

10

10

110

00

00

100

50

10

30

10

­ Num

ber of isolates per type

S. Anatum

1

S. Derby

13

S. Enteritidis

31

1

S. Fyris

1

S. Goldcoast

1

S. Infantis

61

S. M

uenchen

2

S. Saintpaul

1

S. Stanleyville

1

S. Typhimurium

11

11

13

1

Salmonella sp

p.

1

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Footnote

(*) M

: Monitoring, C : Clinical

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2.1.7. Antimicrobial resistance in Salmonella isolates

Antimicrobial resistance is the ability of certain microorganisms to survive or grow in the presence of a givenconcentration of antimicrobial agent that usually would kill or inhibit the microorganism species in question.Antimicrobial resistant Salmonella strains may be transferred from animals or foodstuffs to humans.

A. Antimicrobial resistance in Salmonella in cattle

Sampling strategy used in monitoring

Frequency of the sampling

Subjected to test are isolates obtained within the monitoring of zoonoses and zoonotic agentsand from all other samples tested within National Veterinary Institute. At least one isolate fromeach epidemiological unit.

Type of specimen taken

See the monitoring for Salmonella in bovine animals.

Methods of sampling (description of sampling techniques)

See the monitoring for Salmonella in bovine animals.

Procedures for the selection of isolates for antimicrobial testing

At least one isolate from each epidemiological unit.

Methods used for collecting data

Report of results obtained within the monitoring are reported to the VARS Main Office.

Laboratory methodology used for identification of the microbial isolates

See the monitoring for Salmonella in bovine animals.Disc diffusion method according to the CLSI (former NCCLS).

Laboratory used for detection for resistance

Antimicrobials included in monitoring

Aminoglycosides: streptomycin, neomycin, kanamycin, gentamycin, spectinomycin Amphenicols: Chloramphenicol, fluorphenicolBeta­lactamic: ampicillin and amoxycillin; amoxycillin/ clavulanic acidCephalosporins: cephotaxim,ceftriofur, ceftriaxonQuinolones: nalidixinic acidFluoroquinolones: enrofloxacine, ciprofloxacin, flumequineSulphonamides: sulfonamides,trimethoprim­sulphonamide: trimethoprim/ sulfamethoxazoleTetracyclines: tetracycline

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Breakpoints used in testing

According to CLSI (former NCCLS)

Control program/ mechanisms

Recent actions taken to control the zoonoses

Introduced monitoring.

Notification system in place

NRL­Salmonella reports to VARS at least once a year.

Results of the investigation

Of 4 Salmonella isolates S.Infantis was resistant to Streptomycin, S.Paratyphi B and S.Kottbus werefully sensitive and S.Brancaster was not tested.

National evaluation of the recent situation, the trends and sources of infection

In the year 2006 the situation is considered to be good.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

The spread of multiresistant S. Typhimurium strains indicates that cattle might become a source ofsuch strains for humans, too.

B. Antimicrobial resistance in Salmonella in pigs

Sampling strategy used in monitoring

Frequency of the sampling

Subjected to test are isolates obtained within the monitoring of zoonoses and zoonotic agentsand from all other samples tested within National Veterinary Institute. At least one isolate fromeach epidemiological unit.

Type of specimen taken

See the monitoring for Salmonella in pigs.

Methods of sampling (description of sampling techniques)

See the monitoring for Salmonella in pigs.

Procedures for the selection of isolates for antimicrobial testing

At least one isolate from each epidemiological unit.

Methods used for collecting data

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Report of results obtained within the monitoring in processing plants, are reported to the VARSMain Office.

Laboratory methodology used for identification of the microbial isolates

See the monitoring for Salmonella in pigs.Disc diffusion method according to the CLSI (former NCCLS).

Laboratory used for detection for resistance

Antimicrobials included in monitoring

Aminoglycosides: streptomycin, neomycin, kanamycin, gentamycin, spectinomycin Amphenicols: Chloramphenicol, fluorphenicolBeta­lactamic: ampicillin and amoxycillin; amoxycillin/ clavulanic acidCephalosporins: cephotaxim, ceftiofur, ceftriaxonQuinolones: nalidixinic acidFluoroquinolones: enrofloxacine, ciprofloxacin, flumequineSulphonamides: sulfonamides,trimethoprim­sulphonamide: trimethoprim/ sulfametoxazoleTetracyclines: tetracycline

Breakpoints used in testing

According to CLSI (former NCCLS).

Control program/ mechanisms

Recent actions taken to control the zoonoses

Introduced monitoring.

Notification system in place

NRL­Salmonella reports to VARS at least once a year.

Results of the investigation

One strain of S.Enteritidis and one of S.Infantis were fully susceptible. One strain of group C1 wasresistant to 1 antimicrobial. Of 5 strains of S.Typhimurium 3 were resistant to 6 antimicrobials and 2to 5 antimicrobials including ciprofloxacin.

National evaluation of the recent situation, the trends and sources of infection

Since multiresistant strains of S. Typhimurium were found in pig limph nodes, its spread in pigpopulation should be considered as a potential danger for its spread to humans, too.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

A possible spread of multiresistant S. Typhimurium should be considered and adequate measuresshould be taken to minimise this threat.

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C. Antimicrobial resistance in Salmonella in poultry

Sampling strategy used in monitoring

Frequency of the sampling

Subjected to test are isolates obtained within the monitoring of zoonoses and zoonotic agentsand from all other samples tested within National Veterinary Institute. At least one isolate fromeach epidemiological unit.

Type of specimen taken

See the monitoring for Salmonella in poultry.

Methods of sampling (description of sampling techniques)

See the monitoring for Salmonella in poultry.

Procedures for the selection of isolates for antimicrobial testing

At least one isolate from each epidemiological unit.

Methods used for collecting data

Report of results obtained within the monitoring in processing plants, are reported to the VARSMain Office.

Laboratory methodology used for identification of the microbial isolates

See the monitoring for Salmonella in poultry.Disc diffusion method according to the CLSI (former NCCLS).

Laboratory used for detection for resistance

Antimicrobials included in monitoring

Aminoglycosides: streptomycin, neomycin, kanamycin, gentamycin, spectinomycin Amphenicols: Chloramphenicol, fluorphenicolBeta­lactamic: ampicillin and amoxycillin; amoxycillin/ clavulonic acidCephalosporins: cephotaxim, ceftiofur, ceftriaxonQuinolones: nalidixinic acidFluoroquinolones: enrofloxacine, ciprofloxacinSulphonamides: sulfonamides,trimethoprim­sulphonamide: trimethoprim/ sulfamethoxazoleTetracyclines: tetracycline

Breakpoints used in testing

According to CLSI (former NCCLS)

Control program/ mechanisms

Recent actions taken to control the zoonoses

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Introduced monitoring.

Notification system in place

NRL­Salmonella reports to VARS at least once a year.

Results of the investigation

Of 17 strains of S.Enteritidis and 3 strains of S.Derby all were fully susceptible. Two strains ofS.Infantis and one strain of S.Virchow were resistant to 4 antimicrobials.

National evaluation of the recent situation, the trends and sources of infection

The situation seems to be good. Poultry is not considered to be an important source of multiresistantSalmonella strains for humans.Thus its importance increases with multiresistant strains and the prevalence found in two baselinestudies.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

Although poultry is considered to be a major source of Salmonella for humans, it is not considered tobe the major source of multiresistant strains, too. The most prevalent serovar is S. Enteritidis, which ismuch fully susceptible at the time.

D. Antimicrobial resistance in Salmonella in foodstuff derived from cattle

Sampling strategy used in monitoring

Frequency of the sampling

Subjected to test are isolates obtained within the monitoring of zoonoses and zoonotic agentsand from all other samples tested within National Veterinary Institute. At least one isolate fromeach epidemiological unit.

Type of specimen taken

See the monitoring for Salmonella in bovine meat ­ at procesing plants.

Methods of sampling (description of sampling techniques)

See the monitoring for Salmonella in bovine meat ­ at procesing plants.

Procedures for the selection of isolates for antimicrobial testing

At least one isolate from each epidemiological unit.

Methods used for collecting data

Report of results obtained within the monitoring in procesing plants are reported to the VARSMain Office.

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Laboratory methodology used for identification of the microbial isolates

See the monitoring for Salmonella in bovine meat ­ at procesing plants. Disc diffusion method according to the CLSI (former NCCLS).

Laboratory used for detection for resistance

Antimicrobials included in monitoring

Aminoglycosides: streptomycin, neomycin, kanamycin, gentamycin, spectinomycin Amphenicols: Chloramphenicol, fluorphenicolBeta­lactamic: ampicillin and amoxycillin; amoxycillin/ clavulanic acidCephalosporins: cephotaxim, ceftiofur, ceftriaxonQuinolones: nalidixinic acidFluoroquinolones: enrofloxacine, ciprofloxacin, flumequineSulphonamides: sulfonamides,trimethoprim­sulphonamide: trimethoprim/ sulfamethoxazoleTetracyclines: tetracycline

Breakpoints used in testing

According to CLSI (former NCCLS).

Control program/ mechanisms

Recent actions taken to control the zoonoses

Introduced monitoring.

Notification system in place

NRL­Salmonella reports to VARS at least once a year.

Results of the investigation

Of 11 strains isolated, belonging to 8 serovars, 9 were tested and 2 strains of S.Derby were resistant to4 antimicrobials and 1 strain to 6 antimicrobials. 5 strains were fully susceptible and one untypedstrain was resistant to streptomycin.

National evaluation of the recent situation, the trends and sources of infection

Till 2005 cattle was not considered to be a major source of multiresistant strains of Salmonella, butthe finding of multiresistant S. Typhimurium strains in 2005 and S.Derby in 2006 indicates that thedanger should not be neglected.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

The finding of multiresistant S. Typhimurium strains indicates that the danger of its spread to humansshould not be neglected and the adequate measures should be taken to prevent it as much as possible.

E. Antimicrobial resistance in Salmonella in foodstuff derived from pigs

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Sampling strategy used in monitoring

Frequency of the sampling

Subjected to test are isolates obtained within the monitoring of zoonoses and zoonotic agents.See the monitoring for Salmonella in pig meat ­ at processing plantsLikewise the isolates were selected out of those available at the National Veterinary Institute, atleast one isolate from each epidemiological unit.

Type of specimen taken

See the monitoring for Salmonella in pig meat ­ at processing plants

Methods of sampling (description of sampling techniques)

See the monitoring for Salmonella in pig meat ­ at processing plants

Procedures for the selection of isolates for antimicrobial testing

At least one isolate from each epidemiological unit.

Methods used for collecting data

Report of results obtained within the monitoring in processing plants, are reported to the VARSMain Office.

Laboratory methodology used for identification of the microbial isolates

See the monitoring for Salmonella in pig meat ­ at processing plants.Disc diffusion method according to the CLSI (former NCCLS).

Laboratory used for detection for resistance

Antimicrobials included in monitoring

Aminoglycosides: streptomycin, neomycin, kanamycin, gentamycin, spectinomycin Amphenicols: Chloramphenicol, fluorphenicolBeta­lactamic: ampicillin and amoxycillin; amoxycillin/ clavulanic acidCephalosporins: cephotaxim, ceftiofur, ceftriaxonQuinolones: nalidixinic acidFluoroquinolones: enrofloxacine, ciprofloxacinSulphonamides: sulfonamides,trimethoprim­sulphonamide: trimethoprim/ sulfamethoxazoleTetracyclines: tetracycline

Breakpoints used in testing

According to CLSI (former NCCLS).

Control program/ mechanisms

Recent actions taken to control the zoonoses

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Introduced monitoring.

Notification system in place

NRL­Salmonella reports to VARS at least once a year.

Results of the investigation

Of the 5 strains, 2 S.Muenchen and 1 S.Typhimurium were fully susceptible, while 1 strain ofS.Typhimurium was resistant to 5 and the other to 6 antimicrobials.

National evaluation of the recent situation, the trends and sources of infection

The findings indicate the spread of multiresistant S. Typhimurium strains, so the adequate measuresshould be taken to minimize the risk of its spread to humans.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

The spread of multiresistant Salmonella strains in pigs should be considered as a potential risk forhumans.

F. Antimicrobial resistance in Salmonella in foodstuff derived from poultry

Sampling strategy used in monitoring

Frequency of the sampling

Subjected to test are isolates obtained within the monitoring of zoonoses and zoonotic agentsand from all other samples tested within National Veterinary Institute. At least one isolate fromeach epidemiological unit.

Type of specimen taken

See the monitoring for Salmonella in poultry meat ­ at processing plants.

Methods of sampling (description of sampling techniques)

See the monitoring for Salmonella in poultry meat ­ at processing plants.

Procedures for the selection of isolates for antimicrobial testing

At least one isolate from each epidemiological unit.

Methods used for collecting data

Report of results obtained within the monitoring in processing plants, are reported to the VARSMain Office.

Laboratory methodology used for identification of the microbial isolates

See the monitoring for Salmonella in poultry meat ­ at processing plants.Disc diffusion method according to the CLSI (former NCCLS).

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Laboratory used for detection for resistance

Antimicrobials included in monitoring

Aminoglycosides: streptomycin, neomycin, kanamycin, gentamycin, spectinomycin Amphenicols: Chloramphenicol, fluorphenicolBeta­lactamic: ampicillin and amoxycillin; amoxycillin/ clavulanic acidCephalosporins: cephotaxim, ceftiofur, ceftriaxonQuinolones: nalidixinic acidFluoroquinolones: enrofloxacine, ciprofloxacinSulphonamides: sulfonamides,trimethoprim­sulphonamide: trimethoprim/ sulfamethoxazoleTetracyclines: tetracycline

Breakpoints used in testing

According to CLSI (former NCCLS).

Control program/ mechanisms

Recent actions taken to control the zoonoses

Introduced monitoring.

Notification system in place

NRL­Salmonella reports to VARS at least once a year.

Results of the investigation

In gallus gallus 3 strains of S.Derby, S.Enteritidis and S.Infantis were fully susceptible and 4 strains ofS.Infantis were resistant to 1 antimicrobial and one strain of S.Infantis to 4 antimicrobials. One strainof S.Typhymurium was resistant to 5 antimicrobials.In turkeys 1 strain of S.Enteritidis was fully susceptible, 1 strain of S.Saintpaul was resistant to 1antimicrobial and 4 strain of S.Typhimurium to 5 antimicrobials.

National evaluation of the recent situation, the trends and sources of infection

Although the results of poultry examinations for Salmonella do not indicate the poultry to be themajor source of multiresistant strains, the examiantions of food derived from poutry does notcorroborate this opinion. Turkeys seem to be a possible source of higly multiresistant strains of S.Typhimurium. The other serovars, isolated from poultry, were more susceptible. Regarding bigconsumption of poultry meat, this might become an important source of multiresistant strains forhumans.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

The findings indicate that poultry (specially turkeys) might become an important source ofmultiresistant Salmonella strains for humans.

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Table Antimicrobial su

sceptib

ility testing of S. A

natum in minced meat ­ M

eat from bovine animals

and pig ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­ H

ACCP or own checks by

industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Anatum

­Meat from bovine animals and pig ­ minced meat ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­

HACCP or own checks by industry

Isolates out of a monitoring

programme

Num

ber of isolates available in

the laboratory

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

0

Amphenicols

Chloram

phenicol

0

Florfenicol

0

Cephalosporins

Cefotaxim

0

Ceftiofur

0

Ceftriaxon

0

Fluoroquinolones

Ciprofloxacin

0

Enrofloxacin

0

Quinolones

Nalidixic acid

0

Sulfonamides

Sulfonamide

0

Trimethoprim

0

Aminoglycosides

Streptom

ycin

0

Gentamicin

0

Neomycin

0

Kanam

ycin

0

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Spectinom

ycin

0

Penicillins

Amoxicillin

0

Amoxicillin / Clavulanic acid

0

Ampicillin

0

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

0

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Table Antimicrobial susceptibility testing of S. Derby ­ qualitative data

n = Number of resistant isolates

S. DerbyGallus gallus (fowl) ­ at farm ­ animal sample ­ faeces ­ Surveillance ­ HACCP or own checks byindustry

Isolates out of a monitoringprogramme

no

Number of isolatesavailable in the laboratory

3

­Antimicrobials: N nTetracyclines

Tetracyclin 3 0Amphenicols

Chloramphenicol 3 0Florfenicol 3 0

CephalosporinsCefotaxim 3 0Ceftiofur 3 0Ceftriaxon 3 0

FluoroquinolonesCiprofloxacin 3 0Enrofloxacin 3 0

QuinolonesNalidixic acid 3 0

SulfonamidesSulfonamide 3 0

Trimethoprim 3 0

AminoglycosidesStreptomycin 3 0Gentamicin 3 0Neomycin 3 0Kanamycin 3 0Spectinomycin 3 0

PenicillinsAmoxicillin 3 0Amoxicillin / Clavulanicacid

3 0

Ampicillin 3 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

3 0

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Table Antimicrobial su

sceptib

ility testing of S. D

erby in Gallus gallus (fowl) ­ at farm ­ animal sample ­

faeces ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Derby

­Gallus g

allus (fowl) ­ at farm ­ animal sample ­ faeces ­ Surveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

3

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

30

11

1

Amphenicols

Chloram

phenicol

30

11

1

Florfenicol

30

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

30

21

Ceftiofur

30

11

1

Ceftriaxon

30

12

Fluoroquinolones

Ciprofloxacin

30

3

Enrofloxacin

30

11

1

Quinolones

Nalidixic acid

30

21

Sulfonamides

Sulfonamide

30

11

1

Trimethoprim

00

Aminoglycosides

Streptom

ycin

30

21

Gentamicin

30

11

1

Neomycin

30

3

Kanam

ycin

30

21

Spectinom

ycin

30

3

Penicillins

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Amoxicillin

30

11

1

Amoxicillin / Clavulanic acid

30

11

1

Ampicillin

30

12

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

30

11

1

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Table Antimicrobial susceptibility testing of S. Derby ­ qualitative data

n = Number of resistant isolates

S. DerbyMeat from bovine animals and pig ­ mincedmeat ­ intended to be eaten cooked ­ atslaughterhouse ­ Surveillance ­ HACCP or ownchecks by industry

Meat from poultry, unspecified

Isolates out of a monitoringprogramme

no no

Number of isolatesavailable in the laboratory

3 1

­Antimicrobials: N n N nTetracyclines

Tetracyclin 3 3 1 0Amphenicols

Chloramphenicol 3 1 1 0Florfenicol 3 1 1 0

CephalosporinsCefotaxim 3 0 1 0Ceftiofur 3 0 1 0Ceftriaxon 3 0 1 0

FluoroquinolonesCiprofloxacin 3 0 1 0Enrofloxacin 3 0 1 0

QuinolonesNalidixic acid 3 0 1 0

SulfonamidesSulfonamide 3 3 1 0

Trimethoprim 3 1 1 0

AminoglycosidesStreptomycin 3 3 1 0Gentamicin 3 0 1 0Neomycin 3 1 1 0Kanamycin 3 1 1 0Spectinomycin 3 3 1 0

PenicillinsAmoxicillin 3 0 1 0Amoxicillin / Clavulanicacid

3 0 1 0

Ampicillin 3 0 1 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

3 1 1 0

Fully sensitive 1 1

Resistant to 3antimicrobials

3 2

Resistant to >4antimicrobials

3 1

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Table Antimicrobial su

sceptib

ility testing of S. D

erby in M

eat from poultry, unspecified ­ carcass ­

quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Derby

­Meat from poultry, unspecified ­ carcass

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

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Table Antimicrobial su

sceptib

ility testing of S. D

erby in minced meat ­ M

eat from bovine animals and

pig ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­ H

ACCP or own checks by

industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Derby

­Meat from bovine animals and pig ­ minced meat ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­

HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

3

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

33

3

Amphenicols

Chloram

phenicol

31

11

1

Florfenicol

31

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

30

3

Ceftiofur

30

11

1

Ceftriaxon

30

3

Fluoroquinolones

Ciprofloxacin

30

3

Enrofloxacin

30

12

Quinolones

Nalidixic acid

30

21

Sulfonamides

Sulfonamide

33

3

Trimethoprim

31

11

1

Aminoglycosides

Streptom

ycin

33

3

Gentamicin

30

3

Neomycin

31

12

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Kanam

ycin

31

11

1

Spectinom

ycin

33

3

Penicillins

Amoxicillin

30

11

1

Amoxicillin / Clavulanic acid

30

11

1

Ampicillin

30

12

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

31

11

1

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Gallus gallus (fowl) ­ unspecified ­ at farm

­ animal sample ­ faeces ­ Clinical investigations ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Gallus g

allus (fowl) ­ unspecified ­ at farm ­ animal sample ­ faeces ­ Clinical investigations

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

00

Ceftiofur

00

Ceftriaxon

00

Fluoroquinolones

Ciprofloxacin

00

Enrofloxacin

00

Quinolones

Nalidixic acid

00

Sulfonamides

Sulfonamide

00

Trimethoprim

00

Aminoglycosides

Streptom

ycin

00

Gentamicin

00

Neomycin

00

Kanam

ycin

00

Spectinom

ycin

00

Penicillins

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Amoxicillin

00

Amoxicillin / Clavulanic acid

00

Ampicillin

00

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

00

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in elite breeding flocks for egg production

line ­ G

allus gallus (fowl) ­ hatching eggs ­ at hatchery ­ animal sample ­ eggs ­ M

onitoring ­ official

sampling ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Gallus g

allus (fowl) ­ elite breeding flocks for egg production line ­ hatching eggs ­ at hatchery ­ animal sample ­ eggs

­ Monitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

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Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Gallus gallus (fowl) ­ at farm ­ animal

sample ­ faeces ­ Surveillance ­ HACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Gallus g

allus (fowl) ­ at farm ­ animal sample ­ faeces ­ Surveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

5

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

50

11

21

Amphenicols

Chloram

phenicol

50

12

11

Florfenicol

50

11

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

50

14

Ceftiofur

50

21

11

Ceftriaxon

50

11

3

Fluoroquinolones

Ciprofloxacin

50

11

3

Enrofloxacin

50

11

12

Quinolones

Nalidixic acid

50

12

11

Sulfonamides

Sulfonamide

50

12

11

Trimethoprim

50

11

11

1

Aminoglycosides

Streptom

ycin

50

11

21

Gentamicin

50

11

21

Neomycin

50

31

1

Kanam

ycin

50

12

2

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Spectinom

ycin

50

31

1

Penicillins

Amoxicillin

50

11

11

1

Amoxicillin / Clavulanic acid

50

21

11

Ampicillin

50

13

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

50

21

11

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Sw

ans ­ wild ­ in total ­ Clinical

investigations ­ suspect sam

pling ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Sw

ans ­ wild ­ in total ­ Clinical investigations ­ suspect sam

pling

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Slovenia 2006 Report on trends and sources of zoonoses

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S.Enteritidis in animals

n = Number of resistant isolates

S. EnteritidisCattle (bovineanimals)

Pigs Gallus gallus(fowl)

Turkeys Swans ­ wild ­ intotal ­ Clinicalinvestigations

Ostriches ­ zooanimals ­ at zoo ­Clinicalinvestigations

Isolates out of a monitoringprogramme

no yes yes no no no

Number of isolatesavailable in the laboratory

0 1 18 0 1 1

­Antimicrobials: N n N n N n N n N n N nTetracyclines

Tetracyclin 1 0 18 0 1 1 1 0Amphenicols

Chloramphenicol 1 0 18 0 1 0 1 0Florfenicol 1 0 18 0 1 1 1 0

CephalosporinsCefotaxim 1 0 18 0 1 0 1 0Ceftiofur 1 0 18 0 1 0 1 0Ceftriaxon 1 0 18 0 1 0 1 0

FluoroquinolonesCiprofloxacin 1 0 18 0 1 0 1 0Enrofloxacin 1 0 18 0 1 0 1 0

QuinolonesNalidixic acid 1 0 18 0 1 0 1 0

SulfonamidesSulfonamide 1 0 18 0 1 1 1 0

Trimethoprim 1 0 18 0 1 0 1 0

AminoglycosidesStreptomycin 1 0 18 0 1 0 1 0Gentamicin 1 0 18 0 1 0 1 0Neomycin 1 0 18 0 1 0 1 0Kanamycin 1 0 18 0 1 0 1 0Spectinomycin 1 0 18 0 1 0 1 0

PenicillinsAmoxicillin 1 0 18 0 1 0 1 0Amoxicillin / Clavulanicacid

1 0 18 0 1 0 1 0

Ampicillin 1 0 18 0 1 0 1 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

1 0 18 0 1 0 1 0

Fully sensitive 1 1 18 18 1 1

Resistant to 3antimicrobials

1 1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Ostriches ­ zoo animals ­ at zoo ­ Clinical

investigations ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Ostriches ­ zoo animals ­ at zoo ­ Clinical investigations

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Slovenia 2006 Report on trends and sources of zoonoses

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in fattening pigs ­ Pigs ­ unspecified ­ at

slaughterhouse ­ animal sample ­ lym

ph nodes ­ Monitoring ­ official sam

pling ­ quantitative data

[Diffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Pigs ­ fattening pigs ­ unspecified ­ at slaughterhouse ­ animal sample ­ lym

ph nodes ­ Monitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

10

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

Slovenia 2006 103

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Gallus gallus (fowl) ­ at farm ­ animal

sample ­ faeces ­ Control or eradication programmes ­ national program

mes (no Com

munity

co­financing) ­ official sam

pling ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Gallus g

allus (fowl) ­ at farm ­ animal sample ­ faeces ­ Control or eradication programmes ­ national program

mes (no

Com

munity co­financing) ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

10

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

100

14

41

Amphenicols

Chloram

phenicol

100

15

22

Florfenicol

100

13

32

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

100

28

Ceftiofur

100

12

7

Ceftriaxon

100

15

31

Fluoroquinolones

Ciprofloxacin

100

21

7

Enrofloxacin

100

51

4

Quinolones

Nalidixic acid

100

13

14

1

Sulfonamides

Sulfonamide

100

21

12

31

Trimethoprim

120

22

22

31

Aminoglycosides

Streptom

ycin

100

14

41

Gentamicin

100

54

1

Neomycin

100

36

1

Slovenia 2006 Report on trends and sources of zoonoses

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Kanam

ycin

100

14

41

Spectinom

ycin

100

15

31

Penicillins

Amoxicillin

100

55

Amoxicillin / Clavulanic acid

100

11

24

11

Ampicillin

100

13

42

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

100

14

12

2

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Enteritidis ­ qualitative data

n = Number of resistant isolates

S. EnteritidisMeat from broilers (Gallus gallus) ­mechanically separated meat (MSM) ­ atslaughterhouse ­ Surveillance ­ HACCP or ownchecks by industry

Meat from turkey ­ at slaughterhouse

Isolates out of a monitoringprogramme

no yes

Number of isolatesavailable in the laboratory

3 2

­Antimicrobials: N n N nTetracyclines

Tetracyclin 3 0 2 0Amphenicols

Chloramphenicol 3 0 2 0Florfenicol 3 0 2 0

CephalosporinsCefotaxim 3 0 2 0Ceftiofur 3 0 2 0Ceftriaxon 3 0 2 0

FluoroquinolonesCiprofloxacin 3 0 2 0Enrofloxacin 3 0 2 0

QuinolonesNalidixic acid 3 0 2 0

SulfonamidesSulfonamide 3 0 2 0

Trimethoprim 3 0 2 0

AminoglycosidesStreptomycin 3 0 2 0Gentamicin 3 0 2 0Neomycin 3 0 2 0Kanamycin 3 0 2 0Spectinomycin 3 0 2 0

PenicillinsAmoxicillin 3 0 2 0Amoxicillin / Clavulanicacid

3 0 2 0

Ampicillin 3 0 2 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

3 0 2 0

Fully sensitive 3 3 2 0

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Meat from turkey ­ fresh ­ at

slaughterhouse ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Meat from turkey ­ fresh ­ at slaughterhouse ­ S

urveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

10

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Meat from poultry, unspecified ­ at

slaughterhouse ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Meat from poultry, unspecified ­ at slaughterhouse ­ S

urveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

3

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

30

21

Amphenicols

Chloram

phenicol

30

11

1

Florfenicol

30

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

30

3

Ceftiofur

30

12

Ceftriaxon

30

21

Fluoroquinolones

Ciprofloxacin

30

3

Enrofloxacin

30

21

Quinolones

Nalidixic acid

30

21

Sulfonamides

Sulfonamide

30

11

1

Trimethoprim

30

21

Aminoglycosides

Streptom

ycin

30

21

Gentamicin

30

11

1

Neomycin

30

12

Kanam

ycin

30

21

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

30

3

Penicillins

Amoxicillin

30

3

Amoxicillin / Clavulanic acid

30

11

1

Ampicillin

30

11

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

30

11

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in offal ­ M

eat from turkey ­ liver ­ at

slaughterhouse ­ Monitoring ­ official sam

pling ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Meat from turkey ­ offal ­ liver ­ at slaughterhouse ­ M

onitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Slovenia 2006 Report on trends and sources of zoonoses

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Enteritidis ­ qualitative data

n = Number of resistant isolates

S. EnteritidisFeed material of oil seed or fruit origin ­ soya (bean) derived ­ at feed mill ­ Surveillance ­ HACCP orown checks by industry

Isolates out of a monitoringprogramme

no

Number of isolatesavailable in the laboratory

1

­Antimicrobials: N nTetracyclines

Tetracyclin 1 0Amphenicols

Chloramphenicol 1 0Florfenicol 1 0

CephalosporinsCefotaxim 1 0Ceftiofur 1 0Ceftriaxon 1 0

FluoroquinolonesCiprofloxacin 1 0Enrofloxacin 1 0

QuinolonesNalidixic acid 1 0

SulfonamidesSulfonamide 1 0

Trimethoprim 1 0

AminoglycosidesStreptomycin 1 1Gentamicin 1 0Neomycin 1 0Kanamycin 1 0Spectinomycin 1 0

PenicillinsAmoxicillin 1 0Amoxicillin / Clavulanicacid

1 0

Ampicillin 1 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

1 0

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. E

nteritidis in Feed material of oil seed or fruit origin ­

soya (bean) derived ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Enteritidis

­Feed material of oil seed or fruit origin ­ soya (bean) derived ­ Surveillance ­ H

ACCP or own checks by industry

Isolates out of a monitoring

programme

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

10

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of Salmonella in humans,Salmonella Enteritidis

n = Number of resistant isolates

S. Enteritidishumans

Isolates out of a monitoringprogramme Number of isolatesavailable in the laboratory

211

­Antimicrobials: N nTetracyclines

Tetracyclin 3 0.2Quinolones

Nalidixic acid 15 1.1Sulfonamides

Sulfonamide 12 0.9

Trimethoprim 1 0.1

AminoglycosidesStreptomycin 1 0.1

PenicillinsAmpicillin 17 1.3

Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

2 0.2

Fully sensitive 1267 96.3

Resistant to 1 antimicrobial 46 3.5

Resistant to 2antimicrobials

1 0.1

Resistant to 3antimicrobials

1 0.1

Resistant to 4antimicrobials

0 0

Resistant to >4antimicrobials

0 0

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in unspecified ­ G

allus gallus (fowl) ­ day­old

chicks ­ at hatchery ­ environmental sam

ple ­ Surveillance ­ HACCP or own checks by industry ­

quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Gallus g

allus (fowl) ­ unspecified ­ day­old chicks ­ at hatchery ­ environm

ental sam

ple ­ S

urveillance ­ HACCP or

own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

3

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

30

12

Amphenicols

Chloram

phenicol

30

12

Florfenicol

30

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

30

11

1

Ceftiofur

30

11

1

Ceftriaxon

30

21

Fluoroquinolones

Ciprofloxacin

30

3

Enrofloxacin

30

12

Quinolones

Nalidixic acid

30

21

Sulfonamides

Sulfonamide

30

21

Trimethoprim

30

11

1

Aminoglycosides

Streptom

ycin

30

21

Gentamicin

30

21

Neomycin

30

21

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Kanam

ycin

30

21

Spectinom

ycin

30

11

1

Penicillins

Amoxicillin

30

3

Amoxicillin / Clavulanic acid

30

21

Ampicillin

30

21

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

30

12

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in Cattle (bovine animals) ­ at farm

­ animal

sample ­ faeces ­ M

onitoring ­ official sam

pling ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Cattle (bovine animals) ­ at farm ­ animal sample ­ faeces ­ M

onitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in Pigs ­ fattening pigs ­ at slaughterhouse ­

animal sample ­ lym

ph nodes ­ Monitoring ­ official sam

pling ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Pigs ­ fattening pigs ­ at slaughterhouse ­ animal sample ­ lym

ph nodes ­ Monitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Slovenia 2006 Report on trends and sources of zoonoses

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Infantis ­ qualitative data

n = Number of resistant isolates

S. InfantisCattle (bovine animals) ­ atfarm ­ Monitoring ­ officialsampling

Pigs ­ fattening pigs ­ atslaughterhouse ­ animal sample ­lymph nodes ­ Monitoring ­official sampling

Gallus gallus (fowl) ­ at hatchery

Isolates out of a monitoringprogramme

yes yes

Number of isolatesavailable in the laboratory

1 1 5

­Antimicrobials: N n N n N nTetracyclines

Tetracyclin 1 0 1 0 5 1Amphenicols

Chloramphenicol 1 0 1 0 5 0Florfenicol 1 0 1 0 5 0

CephalosporinsCefotaxim 1 0 1 0 5 0Ceftiofur 1 0 1 0 5 0Ceftriaxon 1 0 1 0 5 0

FluoroquinolonesCiprofloxacin 1 0 1 0 5 0Enrofloxacin 1 0 1 0 5 0

QuinolonesNalidixic acid 1 0 1 0 5 2

SulfonamidesSulfonamide 1 0 1 0 5 1

Trimethoprim 1 0 1 0 5 0

AminoglycosidesStreptomycin 1 0 1 1 5 1Gentamicin 1 0 1 0 5 0Neomycin 1 0 1 0 5 0Kanamycin 1 0 1 0 5 0Spectinomycin 1 0 1 0 5 1

PenicillinsAmoxicillin 1 0 1 0 5 0Amoxicillin / Clavulanicacid

1 0 1 0 5 0

Ampicillin 1 0 1 0 5 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

1 0 1 0 5 1

Fully sensitive 1 0 1 1 5 3

Resistant to 1 antimicrobial 1 1 5 1

Resistant to 4antimicrobials

5 1

Footnote

In poultry 3 from surveillance, 2 from monitoring

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in broilers ­ Gallus gallus (fowl) ­ day­old chicks

­ at hatchery ­ environmental sam

ple ­ M

onitoring ­ official sam

pling ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Gallus g

allus (fowl) ­ broilers ­ day­old chicks ­ at hatchery ­ environm

ental sam

ple ­ M

onitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

2

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

21

11

Amphenicols

Chloram

phenicol

20

11

Florfenicol

20

11

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

20

11

Ceftiofur

20

11

Ceftriaxon

20

11

Fluoroquinolones

Ciprofloxacin

20

11

Enrofloxacin

20

11

Quinolones

Nalidixic acid

22

2

Sulfonamides

Sulfonamide

21

11

Trimethoprim

20

11

Aminoglycosides

Streptom

ycin

21

11

Gentamicin

20

11

Neomycin

20

11

Kanam

ycin

20

11

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Spectinom

ycin

21

11

Penicillins

Amoxicillin

20

11

Amoxicillin / Clavulanic acid

20

11

Ampicillin

20

11

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

20

11

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Infantis ­ qualitative data

n = Number of resistant isolates

S. InfantisMeat from broilers (Gallus gallus) ­ atslaughterhouse

Meat from turkey ­ carcass ­ at slaughterhouse ­Surveillance ­ HACCP or own checks by industry

Isolates out of a monitoringprogramme

no no

Number of isolatesavailable in the laboratory

6 1

­Antimicrobials: N n N nTetracyclines

Tetracyclin 6 1 1 1Amphenicols

Chloramphenicol 6 0 1 0Florfenicol 6 1 1 0

CephalosporinsCefotaxim 6 0 1 0Ceftiofur 6 0 1 0Ceftriaxon 6 0 1 0

FluoroquinolonesCiprofloxacin 6 0 1 0Enrofloxacin 6 0 1 0

QuinolonesNalidixic acid 6 5 1 1

SulfonamidesSulfonamide 6 1 1 1

Trimethoprim 6 0 1 0

AminoglycosidesStreptomycin 6 2 1 1Gentamicin 6 0 1 0Neomycin 6 0 1 0Kanamycin 6 0 1 0Spectinomycin 6 1 1 1

PenicillinsAmoxicillin 6 0 1 0Amoxicillin / Clavulanicacid

6 0 1 0

Ampicillin 6 0 1 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

6 0 1 0

Fully sensitive 6 1

Resistant to 1 antimicrobial 6 4

Resistant to 4antimicrobials

6 1 1 1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in minced meat ­ M

eat from broilers (G

allus

gallus) ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­ H

ACCP or own checks by

industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Meat from broilers (G

allus g

allus) ­ minced meat ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­

HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in M

eat from broilers (G

allus gallus) ­ carcass ­

at slaughterhouse ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Meat from broilers (G

allus g

allus) ­ carcass ­ at slaughterhouse ­ S

urveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

5

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

51

12

11

Amphenicols

Chloram

phenicol

50

11

21

Florfenicol

51

11

21

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

50

11

11

1

Ceftiofur

50

31

1

Ceftriaxon

50

11

21

Fluoroquinolones

Ciprofloxacin

50

11

11

1

Enrofloxacin

50

21

11

Quinolones

Nalidixic acid

55

5

Sulfonamides

Sulfonamide

51

11

11

1

Trimethoprim

50

21

11

Aminoglycosides

Streptom

ycin

51

12

2

Gentamicin

50

23

Neomycin

50

22

1

Kanam

ycin

50

12

2

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Spectinom

ycin

51

11

3

Penicillins

Amoxicillin

50

12

2

Amoxicillin / Clavulanic acid

50

12

2

Ampicillin

50

11

21

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

50

11

11

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. Infantis in M

eat from turkey ­ carcass ­ at

slaughterhouse ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Infantis

­Meat from turkey ­ carcass ­ at slaughterhouse ­ S

urveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

11

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

11

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Stanleyville ­ qualitative data

n = Number of resistant isolates

S. StanleyvilleMoose ­ zoo animal ­ in total ­ Clinical investigations

Isolates out of a monitoringprogramme

no

Number of isolatesavailable in the laboratory

2

­Antimicrobials: N nTetracyclines

Tetracyclin 2 0Amphenicols

Chloramphenicol 2 0Florfenicol 2 0

CephalosporinsCefotaxim 2 0Ceftiofur 2 0Ceftriaxon 2 0

FluoroquinolonesCiprofloxacin 2 0Enrofloxacin 2 0

QuinolonesNalidixic acid 2 0

SulfonamidesSulfonamide 2 0

Trimethoprim 2 0

AminoglycosidesStreptomycin 2 0Gentamicin 2 0Neomycin 2 0Kanamycin 2 0Spectinomycin 2 0

PenicillinsAmoxicillin 2 0Amoxicillin / Clavulanicacid

2 0

Ampicillin 2 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

2 0

Fully sensitive 2 2

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Table Antimicrobial su

sceptib

ility testing of S. Stanleyville in M

oose ­ zoo animal ­ at zoo ­ Clinical

investigations ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Stanleyville

­Moose ­ zoo animal ­ at zoo ­ Clinical investigations

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

2

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

20

11

Amphenicols

Chloram

phenicol

20

11

Florfenicol

20

11

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

20

11

Ceftiofur

20

2

Ceftriaxon

20

11

Fluoroquinolones

Ciprofloxacin

20

11

Enrofloxacin

20

11

Quinolones

Nalidixic acid

20

11

Sulfonamides

Sulfonamide

20

11

Trimethoprim

20

11

Aminoglycosides

Streptom

ycin

20

11

Gentamicin

20

11

Neomycin

20

11

Kanam

ycin

20

11

Spectinom

ycin

20

11

Penicillins

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Amoxicillin

20

11

Amoxicillin / Clavulanic acid

20

11

Ampicillin

20

11

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

20

11

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in Pigs ­ fattening pigs ­ at

slaughterhouse ­ animal sample ­ lym

ph nodes ­ Monitoring ­ official sam

pling ­ quantitative data

[Diffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Pigs ­ fattening pigs ­ at slaughterhouse ­ animal sample ­ lym

ph nodes ­ Monitoring ­ official sam

pling

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

3

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

32

21

Amphenicols

Chloram

phenicol

33

3

Florfenicol

32

21

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

30

21

Ceftiofur

30

21

Ceftriaxon

30

11

1

Fluoroquinolones

Ciprofloxacin

31

12

Enrofloxacin

30

21

Quinolones

Nalidixic acid

33

21

Sulfonamides

Sulfonamide

32

21

Trimethoprim

30

21

Aminoglycosides

Streptom

ycin

33

3

Gentamicin

30

3

Neomycin

30

12

Kanam

ycin

30

21

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

33

3

Penicillins

Amoxicillin

33

11

1

Amoxicillin / Clavulanic acid

33

21

Ampicillin

33

3

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

30

11

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S.Typhimurium in animals

n = Number of resistant isolates

S. TyphimuriumCattle (bovineanimals)

Pigs Gallus gallus (fowl) Turkeys Pigeons ­ wild ­ intotal ­ Monitoring ­monitoring survey

Isolates out of a monitoringprogramme

no yes no no yes

Number of isolatesavailable in the laboratory

0 3 0 0 1

­Antimicrobials: N n N n N n N n N nTetracyclines

Tetracyclin 3 2 1 0Amphenicols

Chloramphenicol 3 3 1 0Florfenicol 3 2 1 0

CephalosporinsCefotaxim 3 0 1 0Ceftiofur 3 0 1 0Ceftriaxon 3 0 1 0

FluoroquinolonesCiprofloxacin 3 1 1 0Enrofloxacin 3 0 1 0

QuinolonesNalidixic acid 3 3 1 0

SulfonamidesSulfonamide 3 2 1 0

Trimethoprim 3 0 1 0

AminoglycosidesStreptomycin 3 3 1 1Gentamicin 3 0 1 0Neomycin 3 0 1 0Kanamycin 3 0 1 0Spectinomycin 3 3 1 0

PenicillinsAmoxicillin 3 3 1 0Amoxicillin / Clavulanicacid

3 3 1 0

Ampicillin 3 3 1 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

3 0 1 0

Resistant to 1 antimicrobial 1 1

Resistant to >4antimicrobials

3 3

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in Pigeons ­ wild ­ in total ­ M

onitoring ­

monitoring su

rvey ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Pigeons ­ wild ­ in total ­ M

onitoring ­ m

onitoring survey

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

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Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Typhimurium ­ qualitativedata

n = Number of resistant isolates

S. TyphimuriumMeat from bovineanimals ­ atslaughterhouse ­Surveillance ­ HACCPor own checks byindustry

Meat from pig ­ atslaughterhouse ­Surveillance ­ HACCPor own checks byindustry

Meat from turkey ­ atslaughterhouse

Meat from broilers (Gallusgallus) ­ carcass ­ atslaughterhouse ­ animalsample ­ neck skin ­Surveillance ­ HACCP orown checks by industry

Isolates out of a monitoringprogramme

no no no no

Number of isolatesavailable in the laboratory

1 2 4 1

­Antimicrobials: N n N n N n N nTetracyclines

Tetracyclin 1 0 2 2 4 4 1 1Amphenicols

Chloramphenicol 1 0 2 1 4 3 1 1Florfenicol 1 0 2 1 4 4 1 1

CephalosporinsCefotaxim 1 0 2 0 4 0 1 0Ceftiofur 1 0 2 0 4 0 1 0Ceftriaxon 1 0 2 0 4 0 1 0

FluoroquinolonesCiprofloxacin 1 0 2 0 4 0 1 0Enrofloxacin 1 0 2 0 4 0 1 0

QuinolonesNalidixic acid 1 0 2 1 4 0 1 0

SulfonamidesSulfonamide 1 0 2 2 4 4 1 1

Trimethoprim 1 0 2 1 4 0 1 0

AminoglycosidesStreptomycin 1 0 2 2 4 4 1 1Gentamicin 1 0 2 0 4 0 1 0Neomycin 1 0 2 1 4 0 1 0Kanamycin 1 0 2 1 4 0 1 0Spectinomycin 1 0 2 1 4 4 1 1

PenicillinsAmoxicillin 1 0 2 2 4 4 1 1Amoxicillin / Clavulanicacid

1 0 2 0 4 2 1 0

Ampicillin 1 0 2 2 4 4 1 1Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

1 0 2 1 4 0 1 0

Fully sensitive 1 1

Resistant to >4antimicrobials

2 2 4 4 1 1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in minced meat ­ M

eat from bovine

animals ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­ H

ACCP or own checks by

industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Meat from bovine animals ­ minced meat ­ intended to be eaten cooked ­ at slaughterhouse ­ Surveillance ­ H

ACCP or

own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

10

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

10

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

10

1

Gentamicin

10

1

Neomycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Kanam

ycin

10

1

Spectinom

ycin

10

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

Slovenia 2006 143

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in offa

l ­ M

eat from turkey ­ liver ­

quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Meat from turkey ­ offal ­ liver

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

3

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

33

21

Amphenicols

Chloram

phenicol

33

3

Florfenicol

33

3

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

30

3

Ceftiofur

30

21

Ceftriaxon

30

12

Fluoroquinolones

Ciprofloxacin

30

3

Enrofloxacin

30

12

Quinolones

Nalidixic acid

30

11

1

Sulfonamides

Sulfonamide

33

3

Trimethoprim

30

12

Aminoglycosides

Streptom

ycin

33

3

Gentamicin

30

11

1

Neomycin

30

3

Kanam

ycin

30

21

Spectinom

ycin

33

3

Penicillins

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Amoxicillin

33

11

1

Amoxicillin / Clavulanic acid

32

21

Ampicillin

33

3

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

30

21

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in M

eat from pig ­ offal ­ Surveillance ­

HACCP or own checks by industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Meat from pig ­ offal ­ Surveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

11

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

11

1

Kanam

ycin

11

1

Spectinom

ycin

10

1

Penicillins

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Amoxicillin

11

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

11

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

11

1

Slovenia 2006 Report on trends and sources of zoonoses

Slovenia 2006 147

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in M

eat from turkey ­ carcass ­ at

slaughterhouse ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Meat from turkey ­ carcass ­ at slaughterhouse ­ S

urveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

11

1

Florfenicol

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

11

1

Penicillins

Amoxicillin

11

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

11

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

Slovenia 2006 149

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in M

eat from pig ­ carcass ­ at

slaughterhouse ­ Surveillance ­ H

ACCP or own checks by industry ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Meat from pig ­ carcass ­ at slaughterhouse ­ S

urveillance ­ HACCP or own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

11

1

Florfenicol

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

11

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

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Spectinom

ycin

11

1

Penicillins

Amoxicillin

11

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

11

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

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Table Antimicrobial su

sceptib

ility testing of S. T

yphimurium in M

eat from broilers (G

allus gallus) ­

carcass ­ at slaughterhouse ­ animal sample ­ neck skin ­ Surveillance ­ H

ACCP or own checks by

industry ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Typhimurium

­Meat from broilers (G

allus g

allus) ­ carcass ­ at slaughterhouse ­ animal sample ­ neck skin ­ Surveillance ­ H

ACCP or

own checks by industry

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

11

1

Florfenicol

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

10

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

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Kanam

ycin

10

1

Spectinom

ycin

11

1

Penicillins

Amoxicillin

11

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

11

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of Salmonella in humans,Salmonella Typhimurium

n = Number of resistant isolates

S. Typhimuriumhumans

Isolates out of a monitoringprogramme Number of isolatesavailable in the laboratory

7

­Antimicrobials: N nTetracyclines

Tetracyclin 35 56.5Quinolones

Nalidixic acid 13 21.0Sulfonamides

Sulfonamide 38 61.3

Trimethoprim 10 16.1

AminoglycosidesStreptomycin 34 54.8Gentamicin 3 4.8Kanamycin 2 3.2

PenicillinsAmpicillin 39 62.9

Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

8 13.8

Fully sensitive 21 33.9

Resistant to 1 antimicrobial 3 4.8

Resistant to 2antimicrobials

1 1.6

Resistant to 3antimicrobials

2 3.2

Resistant to 4antimicrobials

11 17.7

Resistant to >4antimicrobials

24 38.7

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Table Antimicrobial su

sceptib

ility testing of S. V

irchow

in broilers ­ Gallus gallus (fowl) ­ during

rearing period ­ at farm

­ animal sample ­ faeces ­ Clinical investigations ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­S. Virchow

­Gallus g

allus (fowl) ­ broilers ­ during rearing period ­ at farm ­ animal sample ­ faeces ­ Clinical investigations

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

1

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

11

1

Amphenicols

Chloram

phenicol

10

1

Florfenicol

10

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

10

1

Ceftiofur

10

1

Ceftriaxon

10

1

Fluoroquinolones

Ciprofloxacin

10

1

Enrofloxacin

10

1

Quinolones

Nalidixic acid

11

1

Sulfonamides

Sulfonamide

11

1

Trimethoprim

10

1

Aminoglycosides

Streptom

ycin

11

1

Gentamicin

10

1

Neomycin

10

1

Kanam

ycin

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Spectinom

ycin

11

1

Penicillins

Amoxicillin

10

1

Amoxicillin / Clavulanic acid

10

1

Ampicillin

10

1

Trimethoprim + su

lfonamides

Trimethoprim + Sulfamethoxazol

10

1

Slovenia 2006 Report on trends and sources of zoonoses

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Table Antimicrobial susceptibility testing of S. Virchow ­ qualitative data

n = Number of resistant isolates

S. VirchowGallus gallus (fowl) ­ broilers ­ during rearing period ­ at farm ­ animal sample ­ faeces ­ Clinicalinvestigations

Isolates out of a monitoringprogramme

no

Number of isolatesavailable in the laboratory

1

­Antimicrobials: N nTetracyclines

Tetracyclin 1 1Amphenicols

Chloramphenicol 1 0Florfenicol 1 0

CephalosporinsCefotaxim 1 0Ceftiofur 1 0Ceftriaxon 1 0

FluoroquinolonesCiprofloxacin 1 0Enrofloxacin 1 0

QuinolonesNalidixic acid 1 1

SulfonamidesSulfonamide 1 1

Trimethoprim 1 0

AminoglycosidesStreptomycin 1 1Gentamicin 1 0Neomycin 1 0Kanamycin 1 0Spectinomycin 1 1

PenicillinsAmoxicillin 1 0Amoxicillin / Clavulanicacid

1 0

Ampicillin 1 0Trimethoprim + sulfonamides

Trimethoprim +Sulfamethoxazol

1 0

Resistant to 4antimicrobials

1 1

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Table Antimicrobial susceptibility testing of Salmonella spp. in food

n = Number of resistant isolates

Salmonella spp.Meat from bovineanimals

Meat from pig Meat from broilers (Gallusgallus)

Meat from other poultryspecies

Isolates out of a monitoringprogramme

yes

Number of isolatesavailable in the laboratory

5

­Antimicrobials: N n N n N n N n

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Table Antimicrobial susceptibility testing of Salmonella in humans,Salmonella spp.

n = Number of resistant isolates

Salmonella spp.humans

Isolates out of a monitoringprogramme Number of isolatesavailable in the laboratory

235

­Antimicrobials: N nTetracyclines

Tetracyclin 53 3.5Amphenicols

Chloramphenicol 28 1.9Cephalosporins

3rd generationcephalosporins

0 0

FluoroquinolonesCiprofloxacin 2 0.1

QuinolonesNalidixic acid 37 2.5

SulfonamidesSulfonamide 68 4.5

Trimethoprim 17 1.1

AminoglycosidesStreptomycin 53 3.5Gentamicin 3 0.2Kanamycin 3 0.2

PenicillinsAmpicillin 70 4.7

Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

16 1.1

Fully sensitive 1391 92.5

Resistant to 1 antimicrobial 60 4.0

Resistant to 2antimicrobials

3 0.2

Resistant to 3antimicrobials

5 0.3

Resistant to 4antimicrobials

13 0.9

Resistant to >4antimicrobials

32 2.1

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Table Breakpoints for antibiotic resistance testing in Animals

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Salmonella Standard for

breakpointBreakpoint concentration (microg/ ml) Range tested concentration

(microg/ ml)Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

AmphenicolsChloramphenicol NCCLS 30 18 12

Florfenicol 30 20 16

TetracyclinesTetracyclin 30 19 14

FluoroquinolonesCiprofloxacin 5 21 15

Enrofloxacin 5 20 16

QuinolonesNalidixic acid 30 19 13

Trimethoprim 5 16 10

SulfonamidesSulfonamide 300 17 12

AminoglycosidesStreptomycin 10 15 11

Gentamicin 10 15 12

Neomycin 30 17 12

Kanamycin 30 18 13

Spectinomycin 100 18 14

Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

25 16 10

CephalosporinsCefotaxim 30 23 14

Ceftiofur 30 20 16

Ceftriaxon 30 21 13

3rd generationcephalosporins

PenicillinsAmoxicillin 10 17 13

Amoxicillin /Clavulanic acid

30 17 13

Ampicillin 10 17 13

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Table Breakpoints for antibiotic resistance testing in Food

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Salmonella Standard for

breakpointBreakpoint concentration (microg/ ml) Range tested concentration

(microg/ ml)Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

AmphenicolsChloramphenicol NCCLS 30 18 12

Florfenicol 30 20 16

TetracyclinesTetracyclin 30 19 14

FluoroquinolonesCiprofloxacin 5 21 15

Enrofloxacin 5 20 16

QuinolonesNalidixic acid 30 19 13

Trimethoprim 5 16 10

SulfonamidesSulfonamide 300 17 12

AminoglycosidesStreptomycin 10 15 11

Gentamicin 10 15 12

Neomycin 30 17 12

Kanamycin 30 18 13

Spectinomycin 100 18 14

Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

25 16 10

CephalosporinsCefotaxim 30 23 14

Ceftiofur 30 20 16

Ceftriaxon 30 21 13

3rd generationcephalosporins

PenicillinsAmoxicillin 10 17 13

Amoxicillin /Clavulanic acid

30 17 13

Ampicillin 10 17 13

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Table Breakpoints for antibiotic resistance testing in Feedingstuff

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Salmonella Standard for

breakpointBreakpoint concentration (microg/ ml) Range tested concentration

(microg/ ml)Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

AmphenicolsChloramphenicol NCCLS 30 18 12

Florfenicol 30 20 16

TetracyclinesTetracyclin 30 19 14

FluoroquinolonesCiprofloxacin 5 21 15

Enrofloxacin 5 20 16

QuinolonesNalidixic acid 30 19 13

Trimethoprim 5 16 10

SulfonamidesSulfonamide 300 17 12

AminoglycosidesStreptomycin 10 15 11

Gentamicin 10 15 12

Neomycin 30 17 12

Kanamycin 30 18 13

Spectinomycin 100 18 14

Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

25 16 10

CephalosporinsCefotaxim 30 23 14

Ceftiofur 30 20 16

Ceftriaxon 30 21 13

3rd generationcephalosporins

PenicillinsAmoxicillin 10 17 13

Amoxicillin /Clavulanic acid

30 17 13

Ampicillin 10 17 13

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Table Breakpoints for antibiotic resistance testing in Humans

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Salmonella Standard for

breakpointBreakpoint concentration (microg/ ml) Range tested concentration

(microg/ ml)Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

AmphenicolsChloramphenicol 30 17 15 13

Florfenicol TetracyclinesTetracyclin 30 18 16 15

FluoroquinolonesCiprofloxacin 5 20 18 16

Enrofloxacin QuinolonesNalidixic acid 30 18 16 14

Trimethoprim 5 15 13 11

SulfonamidesSulfonamide 300 16 14 13

AminoglycosidesStreptomycin 10 14 13 12

Gentamicin 10 14 13

Neomycin Kanamycin 30 17 15 14

Spectinomycin Trimethoprim + sulfonamidesTrimethoprim +Sulfamethoxazol

25 15 12 13

CephalosporinsCefotaxim Ceftiofur Ceftriaxon 3rd generationcephalosporins

30 22 18 15

PenicillinsAmoxicillin Amoxicillin /Clavulanic acid Ampicillin 10 16 15 14

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2.2. CAMPYLOBACTERIOSIS

2.2.1. General evaluation of the national situation

A. Thermophilic Campylobacter general evaluation

History of the disease and/ or infection in the country

In 1986/ 87 the notification of Campylobacter enteritis started and became obligatory due to Law onInfectious diseases.The number of notified cases decreased from 2000 to 2003 and increased from 2003 to 2005.In 2004 number of notifications increased for 19,4% (compared to 2003); in 2005 number of notifications increased for 2,3 %. In 2006 number of notifications, in compariosnwith 2005, decreased for 13 %.The incidence of infection in 2006 was 47,2 / 100 000 inhabitants. No outbreaks were recordered in last years. The real burden of disease is not known. (The incidence of infections is estimated from data onnotifications).

National evaluation of the recent situation, the trends and sources of infection

In 2004 number of notifications increased for 19,4% (compared to 2003); in 2005 number of notifications increased for 2,3 % and in 2006 number of notifications, incompariosn with 2005, decreased for 13 %.The incidence of infection in 2006 was 47,2 / 100 000 inhabitants. No outbreaks were recordered in last years. The real burden of disease is not known. (The incidence of infections is estimated from data onnotifications).

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

In 2006 representative strains of thermophilic Campylobacter jejuni (71 strains ) and C. coli (27strains), isolated from poultry, were tested for susceptibility to 6 antimicrobials. There was a problemwhich antimicrobials and breakpoints to use, since the CRL for antimicrobial resistance started towork in 2007. Consequently not all antimicrobials later recommended by CRL were included in ourscheme. The differences in generally used schemes (± one dilution) are not so great to prevent somegeneral observations. So our data should be estimated trends indicators. The results are presented indetail in tables. In C. jejuni only 12.7% of the tested strains were fully susceptible and 25.3% ofstrains were resistant to 4 or more antimicrobials. In C. coli there were no fully susceptible strains and48.1% of strains were resistant to 4 or more antimicrobials. Regarding high prevalence ofCampylobacters in poultry such a high percentage of resistant strains might significantly contribute tothe prevalence of resistant strains in humans. Efficient measures to reduce the risk of human exposureto poultry Campylobacters are needed. Poultry and eggs remain potential source of infection.

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2.2.2. Campylobacteriosis in humans

A. Thermophilic Campylobacter in humans

Reporting system in place for the human cases

Campylobacter cases are notifiable by national law on infectious diseases. Medical doctors notifycases on daily basis to local institutes of public health. Local institutes of public health notify diseaseto Institute of Public Health of R. Slovenia. Notification since 1977.

Case definition

According to definitions of EU comission.

Diagnostic/ analytical methods used

Serologic and biochemical identification on CCDA medium, Hyppurat test, Cephalotin and nalidixicacid resistance test.

Notification system in place

Campylobacter cases are notifiable by national Law on Infectious Diseases. Medical doctors notifycases on daily basis to local institutes of public health. (Also laboratories are obliged to notify). Localinstitutes of public health notify disease to Institute of Public Health of R. Slovenia. Medical doctorsalso report outbreaks of campylobacter infections. Notification since 1977.

History of the disease and/ or infection in the country

In 1986/ 87 the notification of Campylobacter enteritis started and became obligatory due to Law onInfectious diseases.The number of notified cases decreased from 2000 to 2003 and increased from 2003 to 2005,decreased again in 2006.In 2004 number of notifications increased for 19,4% (compared to 2003); in 2005 number of notifications increased for 2,3 % in 2006 decreased for 13%.The incidence of infection in 2005 was 54 / 100 000 inhabitants in 2006 47, 1 / 100 000 inhabitants.No outbreaks were recordered in last years. The real burden of disease is not known. (The incidence of infections is estimated from data onnotifications).

Results of the investigation

In 2004 number of notifications increased for 19,4% (compared to 2003); in 2005 number of notifications increased for 2,3 % on 2006 decreased for 13%.The incidence of infection in 2005 was 54 / 100 000 inhabitants, in 2006 47,1 / 100 000 inhabitants.No outbreaks were recordered in last years. The real burden of disease is not known. (The incidence of infections is estimated from data onnotifications).

National evaluation of the recent situation, the trends and sources of infection

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Campylobacter is still the second most frequent pathogen of bacterial gastroenteritis in Slovenia.

Relevance as zoonotic disease

Campylobacter is the second most frequent pathogen of bacterial gastroenteritis in Slovenia. (On the first place is Salmonella spp).

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Table Cam

pylobacter in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.Unknown status

Cam

pylobacter

944

47.1

00

00

944

C. coli

412

41

C. jejuni

852

42.6

852

C. lari

160.8

16

C. sputorum

20.1

2

C. upsaliensis

00

0

Cam

pylobacter sp

p.,

unspecified

331.6

33

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Table Cam

pylobacter in hum

ans ­ Age distribution

C. coli

C. jejuni

C. lari

C. sputorum

Cam

pylobacter sp

p.,

unspecified

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

52

359

3128

00

00

00

22

0

1 to 4 years

84

4139

8554

41

30

00

73

4

5 to 14 years

32

1145

7471

43

11

10

31

2

15 to 24 years

114

7132

6567

10

10

00

63

3

25 to 44 years

31

2160

9466

32

11

01

31

2

45 to 64 years

75

2113

6053

21

10

00

104

6

65 years and older

42

2104

4361

20

20

00

21

1

Age unknown

Total :

41

20

21

852

452

400

16

7 9

2 1

1 33

15

18

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Table Cam

pylobacter in hum

ans ­ Seasonal distribution

C. coli

C. jejuni

C. lari

C. sputorum

C. upsaliensis

Cam

pylobacter sp

p.,

unspecified

Month

Cases

Cases

Cases

Cases

Cases

Cases

January

2 52

0 0

0 3

February

6 20

0 0

0 2

March

1 24

3 0

0 1

April

4 28

0 0

0 1

May

2 109

0 0

0 2

June

2 130

1 1

0 2

July

0 92

2 0

0 3

August

11

105

3 0

0 4

Septem

ber

3 108

1 1

0 7

October

3 73

3 0

0 7

Novem

ber

5 64

1 0

0 1

Decem

ber

2 47

2 0

0 0

not known

Total :

41

852

16

2 0

33

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2.2.3. Campylobacter in foodstuffs

A. Thermophilic Campylobacter in Broiler meat and products thereof

Monitoring system

Sampling strategy

At slaughterhouse and cutting plant

VARSBroiler and turkey meat sampling is carried out in all the registered slaughterhousesand/ or cutting plants. Samples were taken at cutting plants operating within 4 major poultry slaughterhousesand in all other (low capacity) slaughterhouses.A meat sample constitutes an epidemiological unit.Sampling is carried out by official veterinarians.

At retail

HIRSAnnual monitoring programme was prepared with respect to the results of programme/ controls carried out in the previous year, epidemiological situation.The majority of samples were taken in cities with 10000 inhabitants or more andnumber of samples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over thesituation.Sampling carried out by health inspectors.Programme: 100 samples of fresh poultry meat per annum.

Frequency of the sampling

At slaughterhouse and cutting plant

Other: At cutting plants operating within 4 major poultry slaughterhouses, 1 randomsample is taken twice a week, normally 75% of broiler meat and 25% of turkey meat.At low capacity slaughterhouses, 1 random sample is taken once a month.

At retail

Sampling takes place during the months February ­ October

Type of specimen taken

At slaughterhouse and cutting plant

Fresh meat

At retail

Other: Prepacked fresh meat

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Methods of sampling (description of sampling techniques)

At slaughterhouse and cutting plant

A meat sample weighing approximately 300 g is removed by a sterile instrument andstored in a sterile bag. In poultry, the thoracic section is removed.Samples must be delivered to the laboratory in the shortest time possible, andnormally, immediately upon sampling. The period of time elapsing from sampling toanalysis shall by no means exceed 3 days. Prior to analysis, the sample must be chilledat +4 oC (± 2 oC).

At retail

A prepacked fresh meat sample is weighing min. 300 g. Samples must be delivered tothe laboratory in the shortest time possible. The period of time elapsing from samplingto analysis shall by no means exceed 24 hours. The temperature during storage andtransport should not exceed +4 oC.

Definition of positive finding

At slaughterhouse and cutting plant

Positive sample is a sample, where the zoonotic agent has been isolated.

At retail

Positive sample is a sample, where Campylobacter has been isolated.

Diagnostic/ analytical methods used

At slaughterhouse and cutting plant

Bacteriological method: ISO 10272:1995

At retail

Bacteriological method: ISO 10272:1995

Preventive measures in place

GMP, GHP, HACCPFood business operators are introducing the system of additional labelling of poultry meat whichincludes special warning to the customers to treat poultry meat at requested temperature before anyuse.

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of establishments subjected to veterinary controls­ Identification of animal products and their traceability­ Veterinary controls in establishments

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Measures in case of the positive findings or single cases

Business operator was informed about the positive result. The costs of analysis were charged to theowner of the sample.

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.HIRSWhenever zoonotic agent­Campylobacter is detected in samples taken, relevant authorities must beinformed.

Results of the investigation

VARSIn 2006, 415 poultry meat samples at cutting plant were taken.Of 336 broiler meat samples taken, and of 79 turkey meat samples taken, thermophyliccampylobacters were isolated from 134 broiler meat samples (39,88 %)and from 7 turkey meatsamples (8,86%) In most cases, C. jejuni was isolated (76,60 %).HIRSMonitoring in retail:Out of 100 samples of poultry meat taken, 59 samples were positive on presence of thermophylicCampylobacter. Detailed evaluation of data shows that 39 samples (66 % of all positive samples) were positive onpresence of C. jejuni, 13 on presence of C. lari, 6 on presence of C. coli and 1 was positive onpresence of C. hyointestinalis.

National evaluation of the recent situation, the trends and sources of infection

VARSIn comparison to the preceding year (production phase), the situation in 2006 got worse as thepercentage of positive samples of fresh poultry meat at procesing plants increased for almost 7 %.HIRSIn comparison to the preceding year (monitoring in retail), the situation in 2006 got worse as thepercentage of positive samples of poultry meat taken increased for 15 %.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

In the light of positive samples, poultry meat is a possible source of human infection, in particular incase of unsatisfactory thermal treatment or inappropriate food handling.

Additional information

Consumers being additionally informed above importance of adequate heat treating of poultry meatbefore any use and hazard of food cross contamination with kitchen tools previously used for freshpoultry meat would benefit, therefore we are in favour of additional labelling.

B. C.,thermophilic in food

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Monitoring system

Sampling strategy

HIRSMonitoring at retailAnnual monitoring programme was prepared with respect to potential presence of zoonoticagent in specific food.The majority of samples were taken in cities with 10000 inhabitants or more and number ofsamples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over the situation.Sampling carried out by health inspectors.Program:Fresh poultry meat: 100 samples/ year;Cheeses from cow's milk (soft and semi­soft): 30 samples/ year;Sour milk: 10 samples/ year

Frequency of the sampling

Sampling takes place during the months: February ­ October

Methods of sampling (description of sampling techniques)

A sample weighing 300­400 g is removed by sterile instrument and stored in a sterile bag orother sterile container in a case the sample is not prepacked. Samples must be delivered to thelaboratory in the shortest time possible . The period of time elapsing from sampling to analysisshall by no means exceed 24 hours. The temperature during storage and transport should notexceed + 4 oC.

Definition of positive finding

Positive sample is a sample from which Campylobacter thermophilic has been isolated.

Diagnostic/ analytical methods used

Bacteriological test: ISO 10272: 1995

Preventive measures in place

GMP, GHP, HACCP

Measures in case of the positive findings or single cases

Additional sampling was carried out and other necessary enforcement actions.

Notification system in place

Whenever zoonotic agent­Campylobacter thermophilic is detected in samples taken, relevantauthorities must be informed.

Results of the investigation

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HIRSMonitoring at retailOut of 140 samples of poultry meat(n=100) and dairy products taken, 59 samples of poultry meatwere positive on presence of thermophylic Campylobacter .All samples of dairy product (soft cheese and sour milk) taken (n=40) were negative on presencethermophylic Campylobacter .

C. thermophilic Campylobacter spp., unspecified in food ­ Meat from bovineanimals and pig

Monitoring system

Sampling strategy

VARSBovine and porcine meat sampling is carried out in all registered high capacity cutting plants. A meat sample constitutes an epidemiological unit.Sampling is carried out by official veterinarians.

Frequency of the sampling

In bovine meat cutting plants, 1 bovine meat sample is taken every 2 months. According toplan, 20 % of veal, and 80 % of meat of animals for fattening are sampled.In porcine meat cutting plants, 1 porcine meat sample is taken every 2 months. The meat ofpigs for fattening is sampled as well.

Type of specimen taken

Meat

Methods of sampling (description of sampling techniques)

A meat sample weighing approximately 300 g is removed by a sterile instrument and stored in asterile bag. In poultry, the thoracic section is removed.Samples must be delivered to the laboratory in the shortest time possible, and normally,immediately upon sampling. The period of time elapsing from sampling to analysis shall by nomeans exceed 3 days. Prior to analysis, the sample must be chilled at +4 oC (± 2 oC).

Definition of positive finding

Positive sample is a sample, where the zoonotic agent has been isolated.

Diagnostic/ analytical methods used

Bacteriological test:ISO 10272: 1995

Preventive measures in place

GMP, GHP, HACCP

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Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of establishments subjected to veterinary controls­ Identification of animal products and their traceability­ Veterinary controls in establishments

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.Business operator must notify VARS of the presence of Salmonellae in the establishment.

Results of the investigation

In 2006, 159 porcine meat samples, and 154 bovine meat samples were taken. From one porcine meatsample Campylobacter coli was isolated.

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Table Campylobacter in poultry meat

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for thermophilic Cam

pylobacter sp

p.

C. coli

C. lari

C. jejuni

C. upsaliensis

thermophilic Cam

pylobacter sp

p., unspecified

C. hyointestinalis

Meat from broilers (Gallusgallus)

­

fresh (1) ­ HIRS single 25g 100 59 6 13 39 0 0 1

­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 20cm2 336 134 50 0 102 0 0 0

Meat from turkey ­fresh ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 20cm2 79 7 1 0 6 0 0 0

(1) : prepacked

Footnote

Meat from broilers ­ at cutting plant:Units positive for C.jejuni:102 = 84 C.jejuni + 18 C.jejuni and C.coliUnits positive for C.coli:50 = 32 C.coli + 18 C.jejuni and C.coli

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Table Campylobacter in other food

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for thermophilic Cam

pylobacter sp

p.

C. jejuni

C. coli

C. upsaliensis

C. lari

thermophilic Cam

pylobacter sp

p., unspecified

Meat from pig ­fresh ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 20cm2 159 1 0 1 0 0 0

Meat from bovine animals ­fresh ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 20cm2 154 0

Cheeses made from cows' milk ­ ­ ­soft and semi­soft ­ HIRS single 25g 30 0 0 0 0 0 0

Dairy products (excludingcheeses)

­ ­ ­

sour milk ­ HIRS single 25g 10 0 0 0 0 0 0

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2.2.4. Campylobacter in animals

A. Thermophilic Campylobacter in Gallus gallus

Monitoring system

Sampling strategy

VARSSampling is carried out continually throughout the year at the four major registered poultryslaughter establishments. Sampled are broilers raised in the Republic of Slovenia only.Slaughter batch of more than 2000 animals constitutes an epidemiological unit, where aslaughter batch means animals originating from a single flock delivered to the slaughterestablishment in a single means of transport.Sampling is carried out by the slaughterhouse official veterinarians.

Frequency of the sampling

At slaughter

Other: At slaughter establishments, 1 slaughter batch is sampled twice a week, takinginto account that all or most rearing establishments are included in the sampling.

Type of specimen taken

At slaughter

Other: Intact caecum

Methods of sampling (description of sampling techniques)

At slaughter

Sampling is uniformly distributed during the slaughter procedure, depending on theslaughter batch. Sampling commences at the first quarter, and ends at the third quarterof slaughtering a slaughter batch. Example of sampling a slaughter batch including2000 animals: the first animal to be sampled is the one following the 500­th animalslaughtered, and thereafter, each 100­th animal is sampled, and finally, the animalfollowing the 1500­th animal slaughtered is sampled. A final sample must comprisesamples taken from 10 animals.The caecum is removed during evisceration by sterile scissors and stored in a sterileplastic bag. In the laboratory, samples are pooled into a pool sample.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. It is recommended thatthe analyses should commence immediately upon acceptance of samples in thelaboratory. The period of time elapsing from sampling to analysis shall by no meansexceed 3 days. Prior to analysis, the samples must be chilled at +4 oC (± 2 oC) and notexposed to light. In the laboratory, the caecum shall be opened aseptically and the content pooled in 1pool sample.

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Case definition

At slaughter

Positive slaughter batch means a batch, where the zoonotic agent has been isolatedfrom the sample taken.

Diagnostic/ analytical methods used

At slaughter

Bacteriological method: Modified on the basis of ISO 10272: 1995

Other preventive measures than vaccination in place

Persons, who in carrying out a registered activity of breeding or production come into direct contactwith animals, must have thorough knowledge in contagious animal diseases, the prevention thereofand transmissibility to man, and in the regulations governing the protection against contagiousdiseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GAP, GHP, and record keeping.

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of establishments subjected to veterinary controls­ Identification of animal products and their traceability­ Veterinary controls in establishments

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.

Results of the investigation

In 2006, the broiler caecum samples from 311 slaughter batches were taken at slaughterestablishments. Thermophylic campylobacters were detected in 225 samples/ slaughter batches(72,34%). C. jejuni was isolated from 132 samples, C. jejuni and C.coli were isolated from 36samples, C.coli was isolated from 56 samples and C. lari from one sample.In 2006, the turkey caecum samples from 76 slaughter batches were taken at slaughter establishment.Termophylic campilobacters were detected in 48 samples/ slaughter batches (63,16%). C. jejuni wasisolated from 32 samples, C. jejuni and C. coli were isolated from 8 samples and C. coli was isolatedfrom 8 samples.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

A relatively high percentage of positive slaughter batches detected might lead to an increased meatcontamination in case of a less strict observation of the good hygiene practice and internal controlrequirements in slaughterhouses. Contaminated meat poses a threat to public health.

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Table Campylobacter in animals

­ ­

Source of information

Sampling unit

Units tested

Total units positive for thermophilic Cam

pylobacter sp

p.

C. jejuni

C. coli

C. lari

C. upsaliensis

thermophilic Cam

pylobacter sp

p., unspecified

Gallus gallus (fowl) ­ ­ ­broilers ­ ­ ­­ at slaughterhouse ­Monitoring ­ officialsampling ­ objectivesampling (1)

­ VARS slaughterbatch

311 225 168 92 1 0 0

Turkeys ­­ at slaughterhouse ­Monitoring ­ official sampling­ objective sampling (2)

­ VARS slaughterbatch

76 48 40 16 0 0 0

(1) : Intact caeca(2) : Intact caeca

Footnote

Broilers:Units positive for C.jejuni:168 = 132 C.jejuni + 36 C.jejuni and C.coliUnits positive for C.coli:92 = 56 C.coli + 36 C.jejuni and C.coliTurkeys:Units positive for C.jejuni:40 = 32 C.jejuni + 8 C.jejuni and C.coliUnits positive for C.coli:16 = 8 C.jejuni + 8 C.jejuni and C.coli

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2.2.5. Antimicrobial resistance in Campylobacter isolates

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Table Antimicrobial su

sceptib

ility testing of C. coli in Gallus gallus (fowl) ­ at slaughterhouse ­

Monitoring ­ quantitative data [D

ilution method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­C. coli

­Gallus g

allus (fowl) ­ at slaughterhouse ­ M

onitoring

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

27

­ Antimicrobials:

Nn

<=0.03

0.06

0.12

0.25

0.5

12

48

1632

64128

256

512

1024

2048

>2048

lowest

highest

Tetracyclines

Oxytetracyclin

2718

32

31

13

29

3

Tetracyclin

00

Fluoroquinolones

Ciprofloxacin

00

Enrofloxacin

2725

11

15

19

Quinolones

Nalidixic acid

2726

11

27

16

Aminoglycosides

Gentamicin

2712

31

65

72

3

Macrolides

Erythrom

ycin

272

17

47

62

Penicillins

Ampicillin

2718

51

12

42

210

Footnote

With the breakpoint of >

32 for N

alidixic acid there are 25 resistant strains. With the breakpoint of >

2 for G

entamicin there are 5 resistant strains. With the breakpoint

of >16 for A

mpicillin there are 14 resistant strains.

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Table Antimicrobial susceptibility testing of C. coli ­ qualitative data

n = Number of resistant isolates

C. coliGallus gallus (fowl) ­ at slaughterhouse ­ Monitoring

Isolates out of a monitoringprogramme

yes

Number of isolatesavailable in the laboratory

27

­Antimicrobials: N nTetracyclines

Oxytetracyclin 27 18Fluoroquinolones

Enrofloxacin 27 25Quinolones

Nalidixic acid 27 25Aminoglycosides

Gentamicin 27 5Macrolides

Erythromycin 27 2Penicillins

Ampicillin 27 14

Fully sensitive 27 0

Resistant to 1 antimicrobial 27 2

Resistant to 2antimicrobials

27 2

Resistant to 3antimicrobials

27 10

Resistant to 4antimicrobials

27 9

Resistant to >4antimicrobials

27 4

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Table Antimicrobial susceptibility testing of C. jejuni ­ qualitative data

n = Number of resistant isolates

C. jejuniGallus gallus (fowl) ­ at slaughterhouse ­ Monitoring

Isolates out of a monitoringprogramme

yes

Number of isolatesavailable in the laboratory

71

­Antimicrobials: N nTetracyclines

Oxytetracyclin 71 26Fluoroquinolones

Enrofloxacin 71 45Quinolones

Nalidixic acid 71 52Aminoglycosides

Gentamicin 71 14Macrolides

Erythromycin 71 2Penicillins

Ampicillin 71 39

Fully sensitive 71 9

Resistant to 1 antimicrobial 71 12

Resistant to 2antimicrobials

71 10

Resistant to 3antimicrobials

71 22

Resistant to 4antimicrobials

72 12

Resistant to >4antimicrobials

71 6

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Table Antimicrobial su

sceptib

ility testing of C. jejuni in Gallus gallus (fowl) ­ M

onitoring ­ quantitative

data [D

ilution method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­C. jejuni

­Gallus g

allus (fowl) ­ M

onitoring

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

71

­ Antimicrobials:

Nn

<=0.03

0.06

0.12

0.25

0.5

12

48

1632

64128

256

512

1024

2048

>2048

lowest

highest

Tetracyclines

Oxytetracyclin

7126

123

113

52

23

66

9

Tetracyclin

00

Fluoroquinolones

Ciprofloxacin

00

Enrofloxacin

7145

17

135

21

339

Quinolones

Nalidixic acid

7152

12

313

101

635

Aminoglycosides

Gentamicin

7114

85

2420

72

23

Macrolides

Erythrom

ycin

712

131

2122

93

11

Penicillins

Ampicillin

7139

17

106

85

85

21

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Table Antimicrobial susceptibility testing of Campylobacter in humans

n = Number of resistant isolates

Campylobacter spp., unspecifiedhumans

Isolates out of a monitoringprogramme Number of isolatesavailable in the laboratory

69

­Antimicrobials: N nTetracyclines

Tetracyclin 69 9Fluoroquinolones

Ciprofloxacin 69 38Quinolones

Nalidixic acid 69 41Aminoglycosides

Gentamicin 69 1Macrolides

Erythromycin 69 2Penicillins

Ampicillin 69 24

Fully sensitive 69 21

Resistant to 1 antimicrobial 69 7

Resistant to 2antimicrobials

69 16

Resistant to 3antimicrobials

69 24

Resistant to 4antimicrobials

69 1

Resistant to >4antimicrobials

69 0

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Table Breakpoints used for antimicrobial susceptibility testing in Animals

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ EUCAST

­Campylobacter Standard for

breakpointBreakpoint concentration (microg/ ml) Range tested concentration

(microg/ ml)Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

TetracyclinesOxytetracyclin 2 2 0.25 32

Tetracyclin FluoroquinolonesCiprofloxacin Enrofloxacin 0.5 0.5 0.12 4

QuinolonesNalidixic acid 16 16 2 128

AminoglycosidesGentamicin 1 1 0.25 8

MacrolidesErythromycin 4 4 0.12 16

PenicillinsAmpicillin 8 8 0.5 64

Footnote

For Oxytetracycline breakpoints of Tetracycline were used. For Campylobacter coli we used different breakpoints forAmpicillin (>16), Erythromycin (>16), Nalidixic acid (32) and Gentamicin (>2).For Enrofloxacin we use the breakpoints of ...

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Table Breakpoints used for antimicrobial susceptibility testing in Humans

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Campylobacter Standard for

breakpointBreakpoint concentration (microg/ ml) Range tested concentration

(microg/ ml)Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

TetracyclinesOxytetracyclin Tetracyclin 30 19 16 14

FluoroquinolonesCiprofloxacin 5 21 18 15

Enrofloxacin QuinolonesNalidixic acid 30 19 16 13

AminoglycosidesGentamicin 10 15 13 12

MacrolidesErythromycin 15 23 18 13

PenicillinsAmpicillin 10 17 15 13

Footnote

Data are available just for some laboratories with comparable antibiogramme methods. The notificated number of Campylobacter cases is therefore higher.

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2.3. LISTERIOSIS

2.3.1. General evaluation of the national situation

A. Listeriosis general evaluation

History of the disease and/ or infection in the country

In last 5 years 0 to 7 human cases annually were notified.In 2005 three human cases were notified, in 2006 seven.

National evaluation of the recent situation, the trends and sources of infection

Most patients had meningitis.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Listeriosis cases are notifiable by Veterinary Compliance Criteria Act (UL RS 93/ 05). Veterinariusand laboratories are obligated to notify cases of listeriosis. Listeriosis in animals is limited only on sporadic cases. In all positive cases all production animals onthe holding (especially diary ruminants) are tested and eradication measures are suplemented.At the end of 2006 procedure for nomination of National Veterinary Institute for NRL forL.monocytogenes started.

Recent actions taken to control the zoonoses

Epidemiological surveillance of human cases.

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2.3.2. Listeriosis in humans

A. Listeriosis in humans

Reporting system in place for the human cases

Listeriosis cases are notifiable by national Law on infectious diseases (Official Gazette 69/ 95).Medical doctors notify cases on daily basis to local institutes of public health. (Also laboratories areobliged to notify). Local institutes of public health notify disease to Institute of Public Health of R.Slovenia. Notification since 1977.

Case definition

According to definition of commission of the EU communities.

Diagnostic/ analytical methods used

Isolation from body fluids on differential and selective media, Gram staining; biochemical tests;serology;PCR.

Notification system in place

Listeriosis cases are notifiable by national Law on infectious diseases. Medical doctors notify cases ondaily basis to local institutes of public health. (Also laboratories are obliged to notify). Local institutesof public health notify disease to Institute of Public Health of R. Slovenia. Notification since 1977.

History of the disease and/ or infection in the country

In last 5 years 0 to 7 human cases annually were notified.In 2005 three human cases were notified, in 2006 seven ( incidence 0,35/ 100 000 inhabitants).

National evaluation of the recent situation, the trends and sources of infection

In 2005 there were threee and in 2006 seven cases notified.

Relevance as zoonotic disease

Currently not relevant.

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Table Listeria in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.

Listeria

70.35

L. monocytogenes

60.3

Listeria sp

p.1

0.05

Congenital cases

Deaths

10.05

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Table Listeria in hum

ans ­ Age distribution

L. m

onocytogenes

Listeria spp.

Age Distribution

All

MF

All

MF

<1 year

22

00

00

1 to 4 years

00

00

00

5 to 14 years

00

00

00

15 to 24 years

00

00

00

25 to 44 years

10

10

00

45 to 64 years

11

00

00

65 years and older

22

01

10

Age unknown

Total :

6 5

1 1

1 0

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2.3.3. Listeria in foodstuffs

A. L. monocytogenes in food

Monitoring system

Sampling strategy

HIRSMonitoring at retailAnnual monitoring programme was prepared with respect to the results of programme/ controlscarried out in the previous year, epidemiological situation.The majority of samples were taken in cities with 10000 inhabitants or more and number ofsamples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over the situation.Sampling carried out by health inspectors.Programme:Cheeses: 30 samples/ year;Ice­cream: 200 samples/ year;Sour milk: 10 samples/ year;Smoked fish: 20 samples/ year;Molluscan shellfish: 10 samples/ year;Meat from bovine animals and pig (fresh + minced meat): 150 samples/ year;Other processed food products and prepared dishes (deli dishes, pates, sandwiches, meat products,...) 410 samples/ year; Sprouted seeds: 30 samples/ year;Fruits: 20 samples/ year;Vegetables: 80 samples/ year;Sweets (Confectionary products and pastries): 250 samples/ year;Other food of non­animal origin (products in oil): 10 samples/ year

Frequency of the sampling

At retail

Sampling takes place during the months January ­ December

Methods of sampling (description of sampling techniques)

At retail

A sample is weighing 300­400 g is removed by a sterile instrument and stored in asterile bag or other sterile container in a case the sample is not prepacked. Samplesmust be delivered to the laboratory in the shortest time possible. The period of timeelapsing from sampling to analysis shall by no means exceed 24 hours. Thetemperature during storage and transport should not exceed + 4 oC.

Definition of positive finding

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At retail

A sample from which Listeria monocytogenes has been isolated as defined inRegulation 2073/ 2005.

Diagnostic/ analytical methods used

At retail

Bacteriological method: ISO 11290­ 1 and 2:1996, 1998

Preventive measures in place

GMP, GHP, HACCP

Control program/ mechanisms

The control program/ strategies in place

Regular monitoring.

Measures in case of the positive findings

Additional sampling was carried out and other necessary enforcement actions.

Notification system in place

Whenever zoonotic agent­Listeria monocytogenes is detected in samples taken, relevant authorities isinformed.

Results of the investigation

HIRSMonitoring at retailA total of 1220 samples were taken at restaurant, retail and catering. Among all samples taken 4 sample of smoked fish (n=20), 1 sample of vegetables (n=80), 5 samplesof confectionary products and pastries (n=250), 12 samples of red meat (n=50), 8 samples of otherprocessed food products and prepared dishes (n=410) and 35 samples of minced meat (n=100) wereunsuitable due to presence of L. monocytogenes. Out of all 1220 samples taken, 5,3 % were positive on presence of L. monocytogenes. The highestprevalence of Listeria monocytogenes was in samples of minced meat 35 %. All samples of milk and dairy products, products in oil, molluscan shellfish, sprouted seeds andprepacked fruit were negative.

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Table Listeria monocytogenes in milk and dairy products

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for L.monocytogenes

Listeria monocytogenes presence in x g

> detection lim

it but =

< 100 cfu/ g

L. m

onocytogenes > 100 cfu/ g

Cheeses made from cows' milk ­ ­

­

soft and semi­soft ­ ­

­

made from pasteurised milk ­ HIRS single 25g 30 0 0 0 0

Dairy products (excludingcheeses)

­ ­

­

ice­cream ­ HIRS single 25g 200 0 0 0 0

sour milk ­ HIRS single 25g 10 0 0 0 0

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Table Listeria monocytogenes in other foods

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for L.monocytogenes

Listeria monocytogenes presence in x g

> detection lim

it but =

< 100 cfu/ g

L. m

onocytogenes > 100 cfu/ g

Fish ­ ­

­

smoked ­ HIRS single 25g 20 4 4 0 4

Molluscan shellfish ­ ­

­

cooked ­ HIRS single 25g 10 0 0 0 0

Meat from bovine animals andpig

­ ­

­

fresh ­ HIRS single 25g 50 12 12 10 2

minced meat ­ HIRS single 25g 100 35 35 25 10

Other processed food productsand prepared dishes

­ HIRS single 25g 410 8 8 5 3

Sprouted seeds ­ HIRS single 25g 30 0 0 0 0

Fruits ­ ­

­

pre­cut ­ HIRS single 25g 20 0 0 0 0

Vegetables ­ ­

­

non­precut ­ HIRS single 25g 80 1 1 0 1

Confectionery products andpastes

­ HIRS single 25g 250 5 5 3 2

Other food of non­animalorigin

­ ­

­

(products in oil) ­ HIRS single 25g 10 0 0 0 0

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2.3.4. Listeria in animals

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2.4. E. COLI INFECTIONS

2.4.1. General evaluation of the national situation

A. Verotoxigenic Escherichia coli infections general evaluation

History of the disease and/ or infection in the country

Human cases (all E.coli cases) are notifiable by national Law on Infectious Diseases (official Gazettenumber 69/ 95).Medical doctors, laboratories are obliged to notify cases on daily basis to local institutes of publichealth. Local institutes of public health notify disease to Institute of Public Health of R. Slovenia.Most cases are diagnosed and notified as E. coli infection. They are serotyped mostly on O basis,without identification of toxins. VTEC toxins and genes are identified just in two laboratories.(Laboratory of Institute of Public Health of Slovenia and in a laboratory of Medical Faculty inLjubljana). In that way just part of VTEC infections are identified, probably those with more severeclinical picture.Therefore the real burden of VTEC infections is not known.

National evaluation of the recent situation, the trends and sources of infection

The real burden of infection is not known. According to notifications of real VTEC cases(laboratory confirmed ­ VTEC toxin positive and / orvtec genes positive), infection is currently not a problem. No VTEC outbreaks were recorded in recentyears.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

O:157 strains were fully susceptible except for two of 21 strains, resistant to 3 and 4 antimicrobialsrespectively. For now the situation could be considered good, but the possibility of acquiringresistance should not be neglected and monitoring of antimicrobial susceptibility should continue.

Recent actions taken to control the zoonoses

Diagnostics of VTEC should be improved in that way, that all VTEC "suspected samples" should besent to laboratory to confirm toxins/ genes.

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2.4.2. E. Coli Infections in humans

A. Verotoxigenic Escherichia coli infections in humans

Reporting system in place for the human cases

Human cases are notifiable by national Law on Infectious Diseases (official Gazette number 69/ 95).Medical doctors, laboratories are obliged to notify cases on daily basis to local institutes of publichealth. Local institutes of public health notify disease to Institute of Public Health of R. Slovenia.

Case definition

According to EU definitions.

Diagnostic/ analytical methods used

Isolation, biochemial tests, O serotypisation; identification of VT1 and VT2 toxins in Laboratory of Institute of Public Health of Slovenia (RPLAtest) and Microbiological institute of Medical Faculty in Ljubljana.In the latter laboratory also identification of genes is done.

Notification system in place

Human cases are notifiable by national Law on Infectious Diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia.

History of the disease and/ or infection in the country

Real burden of disease is not known.Notification data for all E.coli serotypes: from 1990 to 1999 the average yearly number ofnotifications was about 150 or 7,5 / 100 000 inhabitants. After year 2000 the average yearly number of all E.coli notifications increased to 204 or 10,2/ 100000 inhabitants. According to notifications of real VTEC cases(laboratory confirmed ­ VTEC toxin positive and / orVTEC genes positive), VTEC infections are small part of all E.coli infections.

Results of the investigation

According to notifications of real VTEC cases(laboratory confirmed ­ VTEC toxin positive and / orVTEC genes positive), VTEC infections are small part of all E.coli infections. VTEC infection is nota problem ­ in last years. No VTEC outbreaks were recorded in recent years.

Relevance as zoonotic disease

The real burden of infection is not known. According to notifications of real VTEC (VT1 and VT2 toxins and genes confirmed), the number ofnotifications is low and infection is not a problem yet, no outbreaks were recorded in last years.

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Table Escherichia coli, pathogenic in hum

ans ­ Age distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.

Escherichia coli,

pathogenic

121

6.05

00

00

Verotoxigenic E.

coli (VTE

C)

301.50

Enteropathogenic E.

coli (EPE

C)

391.95

Enterotoxigenic E.

coli (ETE

C)

241.2

Enteroinvasive E.

coli (EIEC)

30.15

E.coli, pathogenic,

unspecified

251.25

HUS

­ clinical cases

­ lab. confirmed

cases

­ caused by O157

(VT+

)

­ caused by other

VTE

C

E.coli infect. (except

HUS)

121

6.05

­ clinical cases

­ laboratory

confirm

ed

121

6.05

­ caused by 0157

(VT+

)

­ caused by other

VTE

C

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Table Escherichia coli, pathogenic in hum

ans ­ Species/ serotype distribution (Part A

)

Verotoxigenic E. coli

(VTEC)

Enteropathogenic E. coli

(EPE

C)

Enterotoxigenic E. coli

(ETEC)

Enteroinvasive E. coli

(EIEC)

E.coli, pathogenic,

unspecified

VTEC O157:H7

Age Distribution

All

MF

All

MF

All

MF

All

MF

All

MF

All

MF

<1 year

31

24

13

53

20

00

44

0

1 to 4 years

53

27

52

21

11

10

64

2

5 to 14 years

86

25

32

00

01

01

30

3

15 to 24 years

44

02

11

21

11

10

22

0

25 to 44 years

31

26

24

63

30

00

75

2

45 to 64 years

30

36

33

51

40

00

21

1

65 years and older

41

39

18

41

30

00

10

1

Age unknown

Total :

30

16

14

39

16

23

24

10

14

3 2

1 25

16

9 0

0 0

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Table Escherichia coli, pathogenic in hum

ans ­ Species/ serotype distribution (Part B

)

VTEC non­O157

Age Distribution

All

MF

<1 year

1 to 4 years

5 to 14 years

15 to 24 years

25 to 44 years

45 to 64 years

65 years and older

Age unknown

Total :

0 0

0

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2.4.3. Escherichia coli, pathogenic in foodstuffs

A. Verotoxigenic E. coli (VTEC) in food

Monitoring system

Sampling strategy

HIRSMonitoring at retailAnnual monitoring programme was prepared with respect to the results of programme/ controlscarried out in the previous year, epidemiological situation.The majority of samples were taken in cities with 10000 inhabitants or more and number ofsamples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over the situation.Sampling carried out by health inspectors.Programme:Red meat: 50 samples / year;Minced meat: 100 samples / year;Vegetables and fruits: 70 samples / year;Sprouted seeds: 30 samples / year;Molluscan shellfish: 10 samples / year

Frequency of the sampling

Sampling takes place during the months: January ­ November

Methods of sampling (description of sampling techniques)

A sample weighing 300 ­ 400 g is removed by sterile instrument and stored in a sterile bag orother sterile container in a case the sample is not prepacked. Samples must be delivered to thelaboratory in the shortest time possible. The period of time elapsing from sampling to analysisshall by no means exceed 24 hours. The temperature during storage and transport should notexceed + 4 oC.

Definition of positive finding

A sample from which Verotoxigenic E.coli has been isolated.

Diagnostic/ analytical methods used

Bacteriological method: ISO 16654: 2001

Preventive measures in place

GMP, GHP, HACCP

Control program/ mechanisms

The control program/ strategies in place

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Regular monitoring

Measures in case of the positive findings or single cases

Additional sampling would be carried out and other necessary enforcement actions.

Notification system in place

Whenever zoonotic agent­VTEC is detected in samples taken, relevant authorities must be informed.

Results of the investigation

HIRSMonitoring at retailA total 260 samples were taken at restaurants, retail and catering. All examined samples were E.coli(VTEC) negative.

B. Verotoxigenic E. coli (VTEC) in food ­ Meat from bovine animals

Monitoring system

Sampling strategy

VARSBovine meat sampling is carried out in all the registered high capacity cutting plants. A meat sample constitutes an epidemiological unit.Sampling is carried out by official veterinarians.

Frequency of the sampling

At cutting plants, 1 meat sample is taken every 2 months.

Type of specimen taken

Meat

Methods of sampling (description of sampling techniques)

A meat sample weighing 300­500 g is removed by a sterile instrument and stored in a sterilebag in a case the sample is not prepacked.Samples must be delivered to the laboratory in the shortest possible time, and normally,immediately upon sampling, i.e. within the same day. During transport, samples must be chilledto +4 oC. Analyses should commence in the shortest possible time after sampling.

Definition of positive finding

Positive sample means a sample, where the zoonotic agent has been isolated from.Isolation of zoonotic agent in 25g.

Diagnostic/ analytical methods used

Bacteriological test:

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ISO 16654: 2001

Preventive measures in place

GMP, GHP, HACCP

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of establishments subjected to veterinary controls­ Identification of animal products and their traceability­ Veterinary controls in establishments

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.

Results of the investigation

In 2006, 153 bovine meat samples were taken. VTEC O:157 was not detected from any sample.

National evaluation of the recent situation, the trends and sources of infection

As compared to year 2005 (5,9 % of positives in sampling at cutting plants), the number of positivecases in 2006 decreased to 0% of positives, and thus we find the situation concerning VTEC in meatfrom bovine animals favourable.

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Table VT E. coli in food

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Escherichia coli, pathogenic

E.coli, pathogenic, unspecified

Verotoxigenic E. coli (VTEC)

Verotoxigenic E. coli (VTEC) ­ VTEC O157

Verotoxigenic E. coli (VTEC) ­ VTEC, unspecified

Meat from bovine animals ­fresh ­­ at cutting plant ­Monitoring ­ officialsampling ­ objectivesampling

­ VARS single 25g 153 0 0 0 0 0

Vegetables ­non­precut ­ HIRS single 25g 50 0 0 0 0 0

Fruits ­pre­cut ­ HIRS single 25g 20 0 0 0 0 0

Meat from bovine animals andpig

­ ­ ­

minced meat ­ HIRS single 25g 100 0 0 0 0 0

fresh ­ HIRS single 25g 50 0 0 0 0 0

Sprouted seeds ­ HIRS single 25g 30 0 0 0 0 0

Molluscan shellfish ­ ­ ­cooked ­ HIRS single 25g 10 0 0 0 0 0

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2.4.4. Escherichia coli, pathogenic in animals

A. Verotoxigenic Escherichia coli in cattle (bovine animals)

Monitoring system

Sampling strategy

VARSSampling is carried out continually throughout the year at all the registered bovineslaughterhouses. Sampled are animals raised in the Republic of Slovenia only.One slaughter animal constitutes an epidemiological unit.Sampling is carried out by the slaughterhouse official veterinarians.

Frequency of the sampling

Animals at slaughter (herd based approach)

Other: One (1) animal per month ­ 1 sample is sampled at slaughter establishments.

Type of specimen taken

Animals at slaughter (herd based approach)

Faeces

Methods of sampling (description of sampling techniques)

Animals at slaughter (herd based approach)

Faeces sample is taken prior to slaughter, and after slaughter, following theevisceration, the intestinal wall is aseptically opened and the intestinal contentremoved from the intestines and stored in a sterile plastic bag.Samples must be delivered to the laboratory in the shortest possible time, andnormally, immediately upon sampling, i.e. within the same day. During transport,samples must be chilled to +4 oC. Analyses should commence in the shortest possibletime after sampling.

Case definition

Animals at slaughter (herd based approach)

Positive animal means an animal, where a positive sample has been taken from.Positive sample means a 10g faeces sample, where the zoonotic agent has been isolatedfrom.

Diagnostic/ analytical methods used

Animals at slaughter (herd based approach)

Bacteriological method: ISO 16654:2001

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Other preventive measures than vaccination in place

Persons, who in carrying out a registered activity of breeding or production, come into direct contactwith animals, foodstuffs, raw materials, products or waste, must have thorough knowledge incontagious animal diseases, the prevention thereof and transmissibility to man, and in the regulationsgoverning the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GAP, GHP, and record keeping.

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of holdings, establishments, transporters, collection centres anddealers, who are subjected to veterinary checks ­ Identified and registered animals­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming from holdings withan unverified or suspect epizootiological situation

Notification system in place

VARS Regional Offices must report to VARS Main Office on a monthly basis regarding themonitoring programme implementation and control results.

Results of the investigation

In 2006, VTEC O:157 was detected in 6 samples (2,6 %) of 235 samples taken.

National evaluation of the recent situation, the trends and sources of infection

As compared to 2005 (5,3 % of positives), the number of positive cases in 2006 decreased by morethan one half (2,6 % positives), and thus we find the situation concerning VTEC in bovine animalsrather favourable.

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Table VT E. coli in animals

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Escherichia coli, pathogenic

E.coli, pathogenic, unspecified

Verotoxigenic E. coli (VTEC)

Verotoxigenic E. coli (VTEC) ­ VTEC O157

Verotoxigenic E. coli (VTEC) ­ VTEC, unspecified

Cattle (bovine animals) ­­ at slaughterhouse ­ animalsample ­ faeces ­ Monitoring ­official sampling ­ objectivesampling

­ VARS animal 235 6 0 6 6 0

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2.5. TUBERCULOSIS, MYCOBACTERIAL DISEASES

2.5.1. General evaluation of the national situation

A. Tuberculosis general evaluation

History of the disease and/ or infection in the country

HumansRegistry of TBC cases of Slovenia was founded in 1954 and has been functioning since then inHospital in Golnik.It is updated regularly. In 1995 it was updated ­reorganized according to demands of WHO and EuroTB.

National evaluation of the recent situation, the trends and sources of infection

Since year 2000 the annual incidence of TBC in Slovenia was lower than 20/ 100 000 inhabitants.About 75% of cases are autochtonous, 25% imported. Imported cases were until recently mostly from Balkan, in last years also from Baltic countries, Chechrepublic, Slovakia, Romunia, Moldowa etc.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Tbc is not relevant as zoonotic disease.

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2.5.2. Tuberculosis, Mycobacterial Diseases in humans

A. Tuberculosis due to Mycobacterium bovis in humans

Reporting system in place for the human cases

Registry of TBC cases of Slovenia was founded in 1954 and has been functioning since then inHospital in Golnik.It is updated regularly. In 1995 it was updated ­reorganized according to demands of WHO and EuroTB.2. Registry on TBC encounters: personnal data of TBC cases,clinical data of TBC cases, data on diagnostic procedures, therapy, data on antimicrobial resistence;data on diagnostics of TBC contacts, HIV patients..;data on BCG vaccination from 2005 on.3. Data on suspected (laboratory unconfirmed) TBC cases are also collated and sent to tbc registry.Further diagnostic procedures are done to confirm new cases.Epidemiological investigations of contacts of suspected cases are also performed. 4. Data on TBC cases in Slovenia are sent to WHO and Euro TB.

Case definition

Tbc case is defined as a person with laboratory confirmed TBC in lungs or other organs.

Diagnostic/ analytical methods used

Mycobacteria are mostly isolated from: (induced) sputum, bronchoscop.,gastric lavage, gastric juice.Bacteria are rarely confirmed in exudates, liquor, biopsy specimen, blood, bone marrow..Ziehl­Neelson and (Auramin dyes in autofluorescent microscope) are used. Lowenstein­Jensen solid medium and MGIT Bactec liquid medium are used.Antimicrobial activity is tested on same media. Identification of types is done with combination of microbiological, molecular and biochemicalmethods.

Notification system in place

Reporting system: medical doctors and laboratories are obliged by law to notify the confirmed TBCcases within one week to the Tbc registry in Hospital Golnik.

History of the disease and/ or infection in the country

Registry of TBC cases of Slovenia was founded in 1954 and has been functioning since then inHospital in Golnik.It is updated regularly. In 1995 it was updated ­reorganized according to demands of WHO and EuroTB.The incidence of all tbc cases in recent years is lower than 20/ 100 000 inhabitants.

Results of the investigation

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In 2006 one case of human infection with Mycobacterium bovis was confirmed.

National evaluation of the recent situation, the trends and sources of infection

Tuberculosis is currently not an epidemiological problem.

Relevance as zoonotic disease

Tbc is not relevant as zoonotic disease.

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Table M

ycobacterium

in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.

Mycobacterium

212

10.65

212

10.65

00

M. bovis

10.05

10.05

M. tuberculosis

211

10.6

211

10.6

Reactivation of

previous cases

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Table M

ycobacterium

in hum

ans ­ Age distribution

M. bovis

M. tuberculosis

Age Distribution

All

MF

All

MF

<1 year

22

0

1 to 4 years

31

2

5 to 14 years

33

0

15 to 24 years

169

7

25 to 44 years

5230

22

45 to 64 years

5237

15

65 years and older

11

8331

52

Age unknown

00

0

Total :

1 1

0 211

113

98

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2.5.3. Mycobacterium in animals

A. Mycobacterium bovis in bovine animals

Status as officially free of bovine tuberculosis during the reporting year

The entire country free

The request for the recognition of status of the entire country was submitted on October 22nd2004.

Monitoring system

Sampling strategy

All animals over 6 weeks of age, compulsory post­ mortem examination of all bovines atslaughter.All samples of lungs of pneumonic cattle older than 2 years are bacteriologically examined forthe presence of M.bovis. All the examinations in 2006 were negative.

Frequency of the sampling

Interval between routine tuberculin test: every two years

Methods of sampling (description of sampling techniques)

Intradermal TB testing accordance with Council Directive 64/ 432/ EEC.

Diagnostic/ analytical methods used

Diagnostic proceduresMycobacterium bovis shall be confirmed by:1. direct microscopic examination of smears of suspect tissues (Ziehl­Neelsen staining,auramine­rodamine staining),2. detecting the characteristic pathohistological changes in the modified tissues (caseousnecroses, epitheloid macrophagues, giant cells),3. immunoperoxidase technique, 4. investigation on cell culture:a. homogenisation, decontamination and concentration of material under examination,cultivation, and selective cell cultures (Lowenstein/ Jensen, Stonebrink, Middlebrook 7H10 or11, MGIT or Middlebrook 7H12),b. cell cultures must be incubated for a minimum of 8 weeks (in the interim, the sediment shallbe kept at –20°C),c. isolate determination is carried out on the basis of the physical and biochemicalcharacteristics, and on the basis of the characteristics of the nucleic acids,d. strain typing is possible by the method of spoligotyping or by the RFLP method,5. detection of the presence of characteristic nucleic acids:a. by the PCR method (AMPLICOR, detection IS6110 or 16s rRNA)b. by the TMA method (GEN­PROBE).TB diagnostics in live animals is based on tuberculin tests.

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Tuberculin tests must be carried out in accordance with the Regulation No. 1226/ 2002/ EC,which is in compliance with the OIE “Manual of standards for diagnostic tests and vaccines,4th edition, 2000”.Under Regulation No. 1226/ 2002/ EC, the maximum number of contaminated animals mayalso be determined on the basis of the gamma interferon test, as detailed in the OIE “Manual ofstandards for diagnostic tests and vaccines, 4th edition, 2000”.In the NVI Laboratory of Bacteriology and Mycology, the methods are used that are indicatedunder items 1, 4a, b, c and 5 above. NVI Lab. is planning to introduce the typing of the M.bovis strains, or to cooperate with the reference laboratories that are carrying it out. At the sametime, NVI Lab. intends to follow the new methods in the diagnostics, in particular in the field ofconfirmation of nucleic acids, and to simultaneously develop new methods on the basis of thequantitative PCR technique.

Measures in case of the positive findings or single cases

Measures at suspected presence of TBWhen upon a sensitisation test with the bovine tuberculin TB is suspected in animals, the followingmeasures shall apply:­ prohibiting the issuing of animal health certificates,­ listing all suspect animals,­ isolating animals,­ restricting the procreation of animals,­ banning the trade in milk and milk products,­ prohibiting the removal of animal feed,­ prohibiting the removal of manure,­ ordering the compulsory packaging of manure for at least 21 days,­ prohibiting the use of common watering points,­ carrying out tests with the bovine and avian tuberculins at the holding, and repeating the tests upon 6weeks .In case of a positive reaction to the repeated test, the animal shall be intended for slaughter, theviscera thereof shall be removed and submitted for investigation to the authorised laboratory. When at slaughter the presence of TB is suspected in the bovine animals, the modified viscera shall besubmitted for investigation to the authorised laboratory. The meat of slaughtered animals shall beassessed by the official veterinarian as unfit for human consumption, when changes are identified onseveral organs or parts of carcass, when increased temperature has been established in the animal priorto slaughter, and when upon slaughter TB­characteristic changes have been established. WhenTB­characteristic changes are localised on some organs or parts of carcass and pertaining lymphnodes, only the affected parts of carcass or organs with the pertaining lymph nodes shall beconsidered unfit for human consumption.Measures at confirmed presence of TB:Epizootiological investigation shall be carried out.The following measures shall apply at the holding, where TB has been detected:­ slaughter of contaminated bovine animals at least within 30 days upon detection,­ cleaning and disinfection of stables, farmyard, watering points and other places, where the suspect ordiseased animals have been kept, as well as of items and installations that have been in contact withsuch animals,­ other measures to sanitise the holding.The official veterinarian at the slaughterhouse shall enter the data on the slaughtered animal in the

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CRBA, cancelling it from the register.Cessation of disease:It shall be considered that the disease has ceased, when all the measures required have been carriedout, and when the next simultaneous tuberculin test upon at least 6 weeks has shown negative resultsin all animals at the holding.The expenses for diagnostic testing are covered from the budget as well as compensation for culledanimals (Rules on the compensations in the veterinary field – Ur. l. RS. št. 37/ 02). Other expenses forthe sanitation of the herd are on the owner of the animals.

Notification system in place

Veterinary Practice Act (Ur. l. RS, št. 33/ 01, 45/ 04) provides a general classification of thecontagious animal diseases, in relation to which the general and specific preventive measures need tobe implemented, and other measures prescribed in the Act, into the Groups A, B and C, in accordancewith the OIE International Animal Health Code, and in accordance with the relevant epizootiologicalsituation. The classification is detailed in the Rules on the contagious animal diseases (Ur. l. RS, št. 54/ 02, 63/ 03 in 28/ 04), where TB is classified among the compulsorily notifiable animal diseases. In the case of an outbreak of contagious animal disease or when signs of disease have beenestablished, constituting reasonable doubt that an animal has taken ill with or died of a contagiousdisease, the holder of the animal in question must immediately and in the prescribed way notifythereof the veterinary organisation (Veterinary Practice Act, Article 12, point 1).In the case of a suspected presence of TB, the relevant veterinary organisation shall notify thereof theRegional Office of the VARS, which shall perform all the necessary measures to prevent the possiblespread of the disease. A report on the outbreak of disease shall be prepared once a month by the tenth day in the month, forthe past month and sent to the VARS HQ.In the case of a zoonosis, the official veterinarian shall notify of the suspected presence of disease alsothe competent public health services.

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Table Bovine tuberculosis in countries and regions that do not receive Com

munity co­fin

ancing for

eradication programmes

Region

Total num

ber of

existin

g bovine

Officially free

herds

Infected herds

Routin

e tuberculin

testing

Num

ber of tuberculin

tests carried out

before the

introduction

Num

ber of animals

with

suspicious

lesions of tuberculosis

Num

ber of animals

detected positive in

bacteriological

exam

ination

Herds

Animals

Num

ber of

herds

%

Num

ber of

herds

%

Interval

between

routine

tuberculin

tests (*)

Num

ber of

animals

tested

into the herds (Annex

A(I)(2

)(c) third

indent (1) of

Directive 64/ 432/

EEC)

exam

ined and

subm

itted to

histopathological and

bacteriological

exam

inations

SLOVEN

IJA

42306

467700

42306

100

0 0

2 444962

0 16

0

Total

42306

467700

42306

100

0 0

444962

0 16

0

(*) L

egend:

In colum

n "Interval between routine tuberculin tests" use the following numeric codes: (0) no routine tests; (1) tests once a year; (2) tests each two years; (3) tests

each three years concerning 24 month­old animals; (4) tests each 4 years; (5) others (please give details).

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2.6. BRUCELLOSIS

2.6.1. General evaluation of the national situation

A. Brucellosis general evaluation

History of the disease and/ or infection in the country

Human cases of brucellosis are notifiable by National law on infectious diseases (Official Gazettenumber 68/ 1995).Medical doctors, laboratories are obliged to notify cases on daily basis to local institutes of publichealth. Local institutes of public health notify disease to Institute of Public Health of R. Slovenia. Brucellosis in Slovenia is notyfiable for more than 50 years.Human infections were generally alimentary and between 1945 and1954 549 cases were registered in littoral Slovenia (Slovensko Primorje) alone.Brucelosis in bovine animals was eradicated in 1961. The disease in goat has been eradicated alreadyin 1955.

National evaluation of the recent situation, the trends and sources of infection

Human brucellosis has been not considered as epidemiological problem for a long time.The danger of reimportation of disease still exists.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Source of infection was in most cases milk, cheese, and milk products.

Recent actions taken to control the zoonoses

Epidemiological and laboratory investigation of all suspected cases.

Suggestions to the Community for the actions to be taken

None, as the disease is not considered as epidemiological problem.

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2.6.2. Brucellosis in humans

A. Brucellosis in humans

Reporting system in place for the human cases

Human cases of brucellosis are notifiable by National law on infectious diseases (Official Gazettenumber 68/ 1995).Medical doctors, laboratories are obliged to notify cases on daily basis to local institutes of publichealth. Local institutes of public health notify disease to Institute of Public Health of R. Slovenia. Brucellosis in Slovenia is notyfiable for more than 50 years.

Case definition

EU comission definitions.

Diagnostic/ analytical methods used

Serological methods;(IF).

Notification system in place

Human cases are notifiable by national law on infectious diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia. Notification after second world war.

History of the disease and/ or infection in the country

Böhm O. Caprine­ovine brucellosis in Istria and the Slovenian littoral in the middle of the 20th:From an epizootiological point of view, the sheep and goat husbandry ofMediterranean Slovenia, Croatian Istria and southeastern Friuli (Isonzo plain) hadsome important attributes. In the middle of the 20th century more than 5,000 sheep,which were transhumant and kept and bred in small flocks of between 50 and 150animals, migrated seasonally to the Isonzo (So~a) plain and western Istria duringwinter, and to the mountainous inland regions during summer. Both the ovine andcaprine Brucella melitensis infections started in the 1930's and became panzooticduring World War II and the years immediately following it.Another epidemiologically important feature was the production of cheeses fromthe ewes' milk. Human infections were generally alimentary and between 1945 and1954 549 cases were registered in littoral Slovenia (Slovensko Primorje) alone.The Yugoslav eradication program, which involved the testing of animals andimmediate culling of reactors, was a radical one. Where 30 % or more of a flocktested positively, the entire flock was eliminated. In 1952 brucellosis was eradicated in Slovenia. The danger of reimportation of disease still exists.

National evaluation of the recent situation, the trends and sources of infection

Human brucellosis is not considered as epidemiological problem for a long time.

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Relevance as zoonotic disease

Human brucellosis is not considered as epidemiological problem for a long time (more than 20 years).

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2.6.3. Brucella in foodstuffs

2.6.4. Brucella in animals

A. Brucella abortus in bovine animals

Monitoring system

Sampling strategy

In 2006, according to the provisions of Annex A Point II. 2. a. second indent of secondparagraph of Council Directive 64/ 432/ EEC testing regime was changed. Since more than 99,8 % herds were recognised as officially brucellosis free for the last fouryears, testing was limited to all animals over 24 months of age in 2006. Rose Bengal has beenused as a screening test and CFT has been used as a confirmatory test. The officially brucellosis free status was suspended in 6 herds (19 animals) by the end of 2006.The reason for suspension was the non­implementation of the prescribed tests. The decisionsuspending the status stipulated the requirements for the renewal of status recognition. Until theprescribed tests are not performed the holdings in question are under restriction (ban onmovements, except for slaughter under official supervision ­ animals from those holdingsintended for slaughter, have to be accompanied with the veterinary referral form).With 2006 testing the provisions for recognition of bovine brucellosis officially free status ofthe country were fulfilled.

Frequency of the sampling

Yearly

Type of specimen taken

Blood

Diagnostic/ analytical methods used

screening test ­ Rose Bengalconfirmatory test ­ CFT

Vaccination policy

Vaccination prohibited

Measures in case of the positive findings or single cases

Rules on the detection, prevention and eradication of brucellosis (Ur. l. RS, st. 91/ 2005, 13/ 2006) Measures at suspected presence of brucellosisAt suspected presence of brucellosis, the authorised veterinary organisation shall immediately confirmor reverse the suspicion, and immediately notify thereof the relevant Regional Office of the VARS,and the NVI. Measures to be implemented at suspect holding include:­ immediate suspension of officially brucellosis free status of the herd;­ quarantine of the infected holding;

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­ ban on movement of susceptible animals inside the holding, taking into account possible vectors ofthe disease;­ isolation of animals susceptible for the disease; milk from those animals can be used for feedinganimals on the same holding after heat treated; milk from other animals on the holding can be used forhuman consumption after heat treated (pasteurized) under official supervision in a dairy plant;­ ban on movement on and from the holding, except for slaughter under official supervision; ­ laboratory examination of carcasses and blood samples;­ epidemiological investigation;­ harmless disposal of dead animals; ­ ban on movement of all animals and stuff by which the disease can be transmitted.The same measures can be introduced also for the holdings that are suspected to be infected.Measures at confirmed presence of brucellosisOnce brucellosis is officially confirmed the following measures are introduced (beside the abovementioned):­ withdrawal of officially brucellosis free status of the herd;­ census of all infected animals on the holding, and animals suspected to be infected;­ ban on trade with animal products, b­products, waste, feeding stuff and all other stuff by which thedisease can be transmitted;­ isolation and slaughter of infected cattle and all cattle suspected to be infected under officialsupervision; cattle has to be slaughtered within 30 days after confirmation of the disease;­ harmless disposal of dead and culled animals, aborted foetuses, placentas and ovarial fluids;­ harmless disposal of waste, manure, litter, by which the disease can be transmitted; ­ cleaning and disinfection. The same measures can be introduced also for the holdings, which are suspected to be infected.Cessation of diseaseThe measures have to be enforced until the conditions for gaining the officially brucellosis free statusof the herd in compliance with the provisions of the Rules on the contagious animal diseases (Ur. l.RS, št. 54/ 02, 63/ 03, 28/ 04 and 142/ 04), which transpose entirely the provisions of CouncilDirective 64/ 432/ EEC in this respect.Procedures applicable to the fresh meat and other eadible partsThe health suitability of meat and other eadible parts is assessed in accordance with the food hygienelegislation:­ Regulation of the European parliament and of the Council of 29 April 2004 laying down specificrules for the organisation of official controls on products of animal origin intended for humanconsumption (EC) No 854/ 2004­ Regulation of the European parliament and of the Council of 29 April 2004 laying down specifichygiene rules for food of animal origin (EC) No 853/ 2004

Notification system in place

Veterinary Compliance Criteria Act (Ur. l. RS, št. 93/ 2005) provides a general classification of thecontagious animal diseases, in relation to which the general and specific preventive measures need tobe implemented, and other measures prescribed in the Act, in accordance with the OIE InternationalAnimal Health Code, and in accordance with the relevant epizootiological situation. The classification is detailed in the Rules on the contagious animal diseases (Ur. l. RS, št. 54/ 02, 63/ 03, 28/ 04 and 142/ 04), where Bovine Brucellosis is classified among the compulsorily notifiableanimal diseases. In the case of an outbreak of contagious animal disease or when signs of disease havebeen established, constituting reasonable doubt that an animal has taken ill with or died of a

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contagious disease, the holder of the animal in question must immediately and in the prescribed waynotify thereof the veterinary organisation (Veterinary Compliance Criteria Act, Article 17).In the case of a suspected presence of bovine brucellosis, the relevant veterinary organisation shallnotify thereof the Regional Office of the VARS, which shall perform all the necessary measures toprevent the possible spread of the disease. A report on the outbreak of disease shall be prepared once a month by the tenth day in the month, forthe past month and sent to the VARS HQ.In the case of a first (primary) outbreak of bovine brucellosis in the country, the designated laboratoryshall immediately communicate the results of diagnostic investigations by telephone and by fax to theVARS HQ.

National evaluation of the recent situation, the trends and sources of infection

Brucelosis was eradicated in 1961.

Additional information

Compulsory notification of all abortions of whatever cause is in place in accordance with CouncilDirective 64/ 432/ EEC.

B. Brucella melitensis in sheep

Status as officially free of ovine brucellosis during the reporting year

The entire country free

Officially free status of ovine/ caprine brucellosis was granted to Slovenia with theCommission Decision 2005/ 179/ EC.

Monitoring system

Sampling strategy

Following the recognition of officially brucellosis (B. melitensis) free status, animals have beentested in accordance with Point II.2.i of Annex A of Council Directive 91/ 68/ EEC (5% of theovine and caprine animals over six months of age).

Frequency of the sampling

Yearly

Methods of sampling (description of sampling techniques)

Individual blood samples

Diagnostic/ analytical methods used

Screening test ­ Rose BengalConfirmatory test ­ CFT

Vaccination policy

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Vacination forbidden

Measures in case of the positive findings or single cases

Measures at suspected presence of brucellosisAt suspected presence of brucellosis, the authorised veterinary organisation shall immediately confirmor reverse the suspicion, and immediately notify thereof the relevant Regional Office of the VARS,and the NVI. Measures to be implemented at suspect holding include:­ laboratory examination of carcasses and blood samples;­ epidemilogical investigation;­ harmless diaposal of dead animals;­ quarantine of the infected holding­ census of all animals on the holding, susceptible for the disease, affected, suspected to be infectedand dead; census shall be up to date, all newborn animals, and animals died during the infection haveto be registered;­ isolation of animals susceptible for the disease,­ ban on movement of susuceptible animals inside the holding, taking into account possible vectors ofthe disease;­ ban on movement on and from the holding;­ ban on movement of all animals and stuff by which the disease can be transmitted;The same measures can be introduced also for the holdings, which are suspected to be infected.Measures at confirmed presence of brucellosisOnce brucellosis is officially confirmed the following measures are introduced (beside the abovementioned):­ ban on trade with animals, animal products, b­products, waste, feeding stuff and all other stuff bywhich the disease can be transmitted;­ slaughter of infected acattle;­ harmless disposal of dead and culled animals, aborted foetuses, placentas and ovarial fluids;­ hrmless disposal of waste, manure, litter, by which the disease can be transmitted;­ testing of all susceptible animals on the holding;­ ban on use of milk from the infected holding;­ ban on use of animals from the infected holding in breeding purposes;­ DDD;The same measures can be introduced also for the holdings, which are suspected to be infected.Cessation of diseaseIt shall be considered that the disease has ceased, when the serological investigation of animals uponthree examinations in an interval of 3 months has shown negative results, and when all theprescribed measures have been implemented.Procedures applicable to the fresh meat and other eadible partsThe health suitability of meat and other eadible parts is assessed in accordance with the food hygienelegislation:­ Regulation of the European parliament and of the Council of 29 April 2004 laying down specificrules for the organisation of official controls on products of animal origin intended for humanconsumption (EC) No 854/ 2004­ Regulation of the European parliament and of the Council of 29 April 2004 laying down specifichygiene rules for food of animal origin (EC) No 853/ 2004

Notification system in place

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Veterinary Compliance Criteria Act (Ur. l. RS, št. 93/ 2005) provides a general classification of thecontagious animal diseases, in relation to which the general and specific preventive measures need tobe implemented, and other measures prescribed in the Act, in accordance with the OIE InternationalAnimal Health Code, and in accordance with the relevant epizootiological situation.The classification is detailed in the Rules on the contagious animal diseases (Ur. l. RS, št. 54/ 02, 63/ 03, 28/ 04 and 142/ 04), where ovine/ caprine brucellosis is classified among the compulsorilynotifiable animal diseases. In the case of an outbreak of contagious animal disease or when signs ofdisease have been established, constituting reasonable doubt that an animal has taken ill with or diedof a contagious disease, the holder of the animal in question must immediately and in the prescribedway notify thereof the veterinary organisation (Veterinary Compliance Criteria Act, Article 17).In the case of a suspected presence of ovine/ caprine brucellosis, the relevant veterinary organisationshall notify thereof the Regional Office of the VARS, which shall perform all the necessary measuresto prevent the possible spread of the disease.A report on the outbreak of disease shall be prepared once a month by the tenth day in the month, forthe past month and sent to the VARS HQ.In the case of a first (primary) outbreak of ovine/ caprine brucellosis in the country, the designatedlaboratory shall immediately communicate the results of diagnostic investigations by telephone and byfax to the VARS HQ.

C. Brucella melitensis in goats

Status as officially free of caprine brucellosis during the reporting year

The entire country free

Officially free status of ovine/ caprine brucellosis was granted to Slovenia with theCommission Decision 2005/ 179/ EC.

Monitoring system

Sampling strategy

Following the recognition of officially brucellosis (B. melitensis) free status, animals have beentested in accordance with Point II.2.i of Annex A of Council Directive 91/ 68/ EEC (5% of theovine and caprine animals over six months of age).

Frequency of the sampling

Yearly

Type of specimen taken

Blood

Methods of sampling (description of sampling techniques)

individual blood samples

Diagnostic/ analytical methods used

­ Rose Bengal test ­ screening test

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­ Complement fixation test ­ confirmatory test

Vaccination policy

Vaccination forbidden

Measures in case of the positive findings or single cases

Measures at suspected presence of brucellosisAt suspected presence of brucellosis, the authorised veterinary organisation shall immediately confirmor reverse the suspicion, and immediately notify thereof the relevant Regional Office of the VARS,and the NVI. Measures to be implemented at suspect holding include:­ laboratory examination of carcasses and blood samples;­ epidemilogical investigation;­ harmless diaposal of dead animals;­ quarantine of the infected holding­ census of all animals on the holding, susceptible for the disease, affected, suspected to be infectedand dead; census shall be up to date, all newborn animals, and animals died during the infection haveto be registered;­ isolation of animals susceptible for the disease,­ ban on movement of susuceptible animals inside the holding, taking into account possible vectors ofthe disease;­ ban on movement on and from the holding;­ ban on movement of all animals and stuff by which the disease can be transmitted;The same measures can be introduced also for the holdings, which are suspected to be infected.Measures at confirmed presence of brucellosisOnce brucellosis is officially confirmed the following measures are introduced (beside the abovementioned):­ ban on trade with animals, animal products, b­products, waste, feeding stuff and all other stuff bywhich the disease can be transmitted;­ slaughter of infected acattle;­ harmless disposal of dead and culled animals, aborted foetuses, placentas and ovarial fluids;­ hrmless disposal of waste, manure, litter, by which the disease can be transmitted;­ testing of all susceptible animals on the holding;­ ban on use of milk from the infected holding;­ ban on use of animals from the infected holding in breeding purposes;­ DDD;The same measures can be introduced also for the holdings, which are suspected to be infected.Cessation of diseaseIt shall be considered that the disease has ceased, when the serological investigation of animals uponthree examinations in an interval of 3 months has shown negative results, and when all theprescribed measures have been implemented.Procedures applicable to the fresh meat and other eadible partsThe health suitability of meat and other eadible parts is assessed in accordance with the food hygienelegislation:­ Regulation of the European parliament and of the Council of 29 April 2004 laying down specificrules for the organisation of official controls on products of animal origin intended for humanconsumption (EC) No 854/ 2004

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­ Regulation of the European parliament and of the Council of 29 April 2004 laying down specifichygiene rules for food of animal origin (EC) No 853/ 2004

Notification system in place

Veterinary Compliance Criteria Act (Ur. l. RS, št. 93/ 2005) provides a general classification of thecontagious animal diseases, in relation to which the general and specific preventive measures need tobe implemented, and other measures prescribed in the Act, in accordance with the OIE InternationalAnimal Health Code, and in accordance with the relevant epizootiological situation. The classification is detailed in the Rules on the contagious animal diseases (Ur. l. RS, št. 54/ 02, 63/ 03, 28/ 04 and 142/ 04), where ovine/ caprine brucellosis is classified among the compulsorilynotifiable animal diseases. In the case of an outbreak of contagious animal disease or when signs ofdisease have been established, constituting reasonable doubt that an animal has taken ill with or diedof a contagious disease, the holder of the animal in question must immediately and in the prescribedway notify thereof the veterinary organisation (Veterinary Compliance Criteria Act, Article 17).In the case of a suspected presence of ovine/ caprine brucellosis, the relevant veterinary organisationshall notify thereof the Regional Office of the VARS, which shall perform all the necessary measuresto prevent the possible spread of the disease. A report on the outbreak of disease shall be prepared once a month by the tenth day in the month, forthe past month and sent to the VARS HQ.In the case of a first (primary) outbreak of ovine/ caprine brucellosis in the country, the designatedlaboratory shall immediately communicate the results of diagnostic investigations by telephone and byfax to the VARS HQ.

Additional information

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Table Bovine brucellosis in countries and regions that do not receive Com

munity co­fin

ancing for

eradication programme

Region

Total num

ber

of

Officially free

herds

Infected

herds

Surveillance

Investigations of suspect cases

existin

gbovine

Serological tests

Examination of bulk

milk samples

Inform

ation about

abortions

Epidemiological investigation

Herds

Animals

Num

ber of

herds

%

Num

ber of

herds

%

Num

ber of

bovine

Num

ber of

animals

Num

ber of

infected

Num

ber of

bovine

Num

ber of

animals

Num

ber of

infected

Num

ber of

notified

Num

ber of

isolations

Num

ber of

abortions

Num

ber of

animals

Num

ber of

suspended

Num

ber of positive animals

Num

ber of

animals

Num

ber of

animals

herds tested

tested

herds tested

herds tested

or pools tested

herds

abortions

whatever cause

of Brucella

infection

due to Brucella

abortus

tested with

serological

blood tests

herds

Serologically

BST

exam

ined

microbio

logically

positive

microbio

logically

SLOVEN

IJA

42306

467700

42300

99.986

0 0

35983

210997

0 0

0 0

182

0 0

0 0

0 0

0 0

Total

42306

467700

42300

99.986

0 0

35983

210997

0 0

0 0

182

0 0

0 0

0 0

0 0

Footnote

The officially brucellosis free status was su

spended in 6 herds (19 animals) by the end of 2006. The reason for suspension was the non­implem

entation of the

prescribed tests. The decision su

spending the status stipulated the requirements for the renewal of status recognition. Until the prescribed tests are not performed the

holdings in question are under restriction (ban on movem

ents, except for slaughter under official supervision ­ animals from those holdings intended for slaughter,

have to be accompanied with the veterinary referral form).

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Ovine or Caprine Brucellosis in countries and regions that do not receive Com

munity co­fin

ancing for

eradication programme

Region

Total num

ber of

existin

g ovine /

caprine

Officially free herds

Infected herds

Surveillance

Investigations of suspect cases

Herds

Animals

Num

ber of herds

%

Num

ber of herds

%

Num

ber of herds

tested

Num

ber of animals

tested

Num

ber of infected

herds

Num

ber of animals

tested with

serological

blood tests

Num

ber of animals

positive serologically

Num

ber of animals

exam

ined microbio

logically

Num

ber of animals

positive microbio

logically

Num

ber of su

spended

herds

SLOVEN

IJA

6737

158288

6737

100

0 0

838

4770

0 0

0 0

0 0

Total

6737

158288

6737

100

0 0

838

4770

0 0

0 0

0 0

Footnote

Officially free status of the country was granted to Slovenia with the Com

mission Decision 2005/ 179/ E

C. Following the recognition of officially brucellosis (B.

melitensis) free status, animals h

ave been tested in accordance with Point II.2.i of Annex A of C

ouncil Directive 91/ 68/ EEC

(5% of the ovine and caprine animals

over six months o

f age).

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2.7. YERSINIOSIS

2.7.1. General evaluation of the national situation

A. Yersinia enterocolitica general evaluation

History of the disease and/ or infection in the country

Yersiniosis is rarely reported in Slovenia.Nevertheless the number of notificated cases increased from 28 in 2005 to 80 in 2006. (The incidenceincreased from 1,4 to 4 / 100 000 inhabitants. The reason of the recent trend is not known yet.The average number of yearly notifications from 2002 to 2006 was 57 or average incidence, based onnotifications, was cca 2,9/ 100 000 inhabitants. From 1990 to 1999 the number of yearly notifications were low as well, except in 1995, the number ofnotifications increased to 1092 or incidence, based on notifications, was cca 54/ 100 000 inhabitants.

National evaluation of the recent situation, the trends and sources of infection

Yersinia enterocolitica is notifiable by national Law on Infectious diseases. Medical doctors notifycases on daily basis to local institutes of public health. Local institutes of public health notify diseaseto Institute of Public Health of R. Slovenia. Notification since 1977.

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2.7.2. Yersiniosis in humans

A. Yersinosis in humans

Reporting system in place for the human cases

Yersinia enterocolitica is notifiable by national Law on Infectious diseases. Medical doctors notifycases on daily basis to local institutes of public health. Local institutes of public health notify diseaseto Institute of Public Health of R. Slovenia. Notification since 1977.

Case definition

According to definition of EU comission.

Diagnostic/ analytical methods used

Isolation on differential and selective media;Gram staining;biochemical identification;serological tests.

Notification system in place

Yersinia enterocolitica is notifiable by national Law on Infectious diseases ( Official Gazette 69/ 95).Medical doctors notify cases on daily basis to local institutes of public health. Local institutes ofpublic health notify disease to Institute of Public Health of R. Slovenia. Notification since 1977.

History of the disease and/ or infection in the country

Yersiniosis is rarely reported in Slovenia.The average number of yearly notifications in last five years was 52 or average incidence, based onnotifications, was cca 2,6/ 100 000 inhabitants. From 1990 to 1999 the number of yearly notifications were low as well, except in 1995, the number ofnotifications increased to 1092 or incidence, based on notifications, was cca 54/ 100 000 inhabitants.

Results of the investigation

The number of notificated cases increased from 28 in 2005 to 80 in 2006. (The incidence increasedfrom 1,4 to 4 / 100 000 inhabitants. The reason of the recent trend is not known yet.

National evaluation of the recent situation, the trends and sources of infection

The real burden of disease is not known because of undereporting of disease.

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Table Yersinia in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.

Yersinia

804

00

069.55

Y. enterocolitica

693.45

69

Yersinia spp.,

unspecified

100.50

0.50

Y. kristensenii

10.05

0.05

Y. enterocolitica ­

O:3

Y. enterocolitica ­

O:9

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Table Yersinia in hum

ans ­ Age distribution

Y. enterocolitica

Yersinia spp.

Y. kristensenii

Age Distribution

All

MF

All

MF

All

MF

<1 year

21

10

00

00

0

1 to 4 years

167

94

13

00

0

5 to 14 years

129

32

20

00

0

15 to 24 years

95

40

00

00

0

25 to 44 years

157

81

01

00

0

45 to 64 years

75

22

11

10

1

65 years and older

84

41

01

00

0

Age unknown

Total :

69

38

31

10

4 6

1 0

1

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Table Yersinia in hum

ans ­ Seasonal distribution

Y. enterocolitica

Yersinia spp.

Y. kristensenii

Month

Cases

Cases

Cases

January

4 3

1

February

2 2

0

March

3 0

0

April

3 0

0

May

3 1

0

June

6 0

0

July

6 0

0

August

14

2 0

Septem

ber

14

0 0

October

6 0

0

Novem

ber

3 1

0

Decem

ber

5 1

0

not known

Total :

69

10

1

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2.7.3. Yersinia in foodstuffs

A. Y. enterocolitica in food

Monitoring system

Sampling strategy

HIRSMonitoring at retailAnnual monitoring programme was prepared with respect to the results of programme/ controlscarried out in the previous year, epidemiological situation.The majority of samples were taken in cities with 10000 inhabitants or more and numberof samples taken was proportional with the population in the region.There were taken at the retail level where sampling could give an overview over thesituation.Sampling carried out by health inspectors.Programme:Red meat: 50 samples / year;Other processed food products and prepared dishes (deli dishes, pates): 360 samples / year

Frequency of the sampling

Sampling takes place during the months: January ­ November

Methods of sampling (description of sampling techniques)

A sample weighing 300 ­ 400 g is removed by sterile instrument and stored in a sterile bag orother sterile container in a case the sample is not prepacked. Samples must be delivered to thelaboratory in the shortest time possible. The period of time elapsing from sampling to analysisshall by no means exceed 24 hours. The temperature during storage and transport should notexceed + 4 oC.

Definition of positive finding

Sample shall be considered positive where the causative agent has been isolated from thesample.

Diagnostic/ analytical methods used

Bacteriological method: ISO 10273:1994

Preventive measures in place

GMP, GHP, HACCP

Control program/ mechanisms

The control program/ strategies in place

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Regular monitoring.

Measures in case of the positive findings or single cases

Additional sampling was carried out and other necessary enforcement actions.

Results of the investigation

HIRSMonitoring at retailA total 410 samples were taken at restaurants, retail and catering.Among all samples taken 3 samples of red meat (n=50) and 3 samples of other processed foodproducts and prepared dishes (n= 360) were unsuitable due to presence of Yersinia enterocolitica.Altogether Yersinia enterocolitica was detected in 1,5 % of food in retail.

National evaluation of the recent situation, the trends and sources of infection

In comparison to the preceding year (monitoring in retail), the situation in 2006 show someimprovement as the percentage of positive samples taken decreased.

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Table Yersinia in food

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Yersinia spp.

Y. enterocolitica

Yersinia spp., unspecified

Y. enterocolitica ­ O:3

Y. enterocolitica ­ O:9

Y. enterocolitica ­ unspecified

Meat from bovine animals andpig

­ HIRS single 25g 50 3 3 0 0 0 3

Other processed food productsand prepared dishes

­ ­ ­

unspecified ­ ­ ­ready­to­eat foods ­ HIRS single 25g 360 3 3 0 0 0 3

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2.7.4. Yersinia in animals

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2.8. TRICHINELLOSIS

2.8.1. General evaluation of the national situation

A. Trichinellosis general evaluation

History of the disease and/ or infection in the country

Human cases are notifiable by National Law on Infectious Diseases (official Gazette number 69/ 1995). Medical doctors are obliged to notify cases on daily basis to local institutes of public health. Localinstitutes of public health notify disease to Institute of Public Health of R. Slovenia. Notification since1977.

National evaluation of the recent situation, the trends and sources of infection

Trichinellosis is a rare human disease in Slovenia. No cases were notified in 2004 and 05, in 2006 onecase.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Trichinellosis is a rare zoonosis in Slovenia. No human cases were recorded in last years, also 2005. In 2006 one case was notified.Most of sporadic cases in last 20 years were infected because of ingestion of imported meat.

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2.8.2. Trichinellosis in humans

A. Trichinellosis in humans

Reporting system in place for the human cases

Human cases are reported by practitioners who are obliged to notify cases on daily basis to localinstitutes of public health. Local institutes of public health notify disease to Institute of Public Healthof Republic Slovenia.

Case definition

According to definition of commission of the EU communities.

Diagnostic/ analytical methods used

Serological tests, parasite cysts in bioptic specimen of skeletal muscle.

Notification system in place

Human cases are notifiable by National Law on Infectious Diseases (official Gazette number 68/ 1995). Medical doctors are obliged to notify cases on daily basis to local institutes of public health. Localinstitutes of public health notify disease to Institute of Public Health of R. Slovenia. Notification since1977.

History of the disease and/ or infection in the country

Trichinellosis is a rare zoonosis in Slovenia. No human cases were recorded in last years, also 2005.Most of sporadic cases in last 20 years were infected because of ingestion of imported meat.In 1989 an outbreak was recorded. 39 people were infected. The source of infection was pork. in thesame year there were also 5 sporadic cases. Another outbreak occured in 1996, 7 people were infected. The source of infection was pork,imported from Croatia.In 1992 42­years old man died from encephalitis due to T. spiralis.

Results of the investigation

Trichinellosis is a rare human disease in Slovenia. No one case was notified in 2004 and 2005.

Description of the positive cases detected during the reporting year

There was one reported human case.

National evaluation of the recent situation, the trends and sources of infection

A rare disease in Slovenia.

Relevance as zoonotic disease

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In the moment not important as zoonotic disease.

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Table Trichinella in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.

Trichinella

10.05

00

00

Trichinella sp

p.1

0.05

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Table Trichinella in hum

ans ­ Age distribution

Trichinella sp

p.

Age Distribution

All

MF

<1 year

00

0

1 to 4 years

00

0

5 to 14 years

00

0

15 to 24 years

00

0

25 to 44 years

11

0

45 to 64 years

00

0

65 years and older

00

0

Age unknown

Total :

1 1

0

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2.8.3. Trichinella in animals

A. Trichinella in pigs

Monitoring system

Sampling strategy

General

VARSThe disease, or the larval stage of the agent of disease, is monitored within the scope ofcompulsory veterinary post­mortem examination of animals at slaughter.Fresh meat of all porcine animals is systematically inspected for Trichinella atslaughterhouses. Likewise, any holder of a tourist farm activity must provide for theinspection of meat obtained from the on­farm slaughtered porcine animals for thepresence of larvae. Epidemiological unit is the animal.

Frequency of the sampling

General

All porcine animals slaughtered are subjected to inspection – either at registeredslaughterhouses or at tourist farms.

Type of specimen taken

General

Fresh meat: diaphragm, lingual muscle, jaw muscle, abdominal muscles as appropriate.

Methods of sampling (description of sampling techniques)

General

In accordance with a reference detection method (artificial digestion of a pooledsample in a magnetic stirrer) or trichinoscopy.

Case definition

General

The disease shall be considered officially confirmed by identifying the agent ofdisease; in the opposite case it shall be considered that the disease has officially beenruled out.Positive animal – animal where Trichinella spp. has been detected.

Diagnostic/ analytical methods used

General

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­ the magnetic stirrer method for pooled sample digestion­ trichinoscopic examination

Preventive measures in place

Persons, who in carrying out a registered activity of breeding or production come into direct contactwith animals, foodstuffs, raw materials, products or waste, must have thorough knowledge incontagious animal diseases, the prevention thereof and transmissibility to man, and in the regulationsgoverning the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GHP, and record keeping.

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of holdings, establishments, transporters, collection centres anddealers, who are subjected to veterinary checks ­ Identified and registered animals­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming from holdings withan unverified or suspect epizootiological situation­ Holder of a tourist farm activity shall at least 48 hours prior to slaughtering porcine animalsnotify an official veterinarian of the relevant Regional Office of VARS, who shall carry out theante­mortem examination of animals prior to slaughter and a post­mortem examination of themeat upon slaughter. Holder of activity shall provide for the examination of porcine meat forthe presence of trichinae.­ Where the meat is intended for placing on the market it shall be ensured that the fresh meat, incase it has not been examined for trichinae, is subjected to freezing process.­ In case of a suspected presence of disease, the disease shall be confirmed or ruled out.­ Measures for the detection, prevention and suppression of disease.

Measures in case of the positive findings or single cases

At the infected holding there shall be:­ instituted an epizootiological investigation;­ provided and maintained the required conditions of hygiene in the facilities;­ banned the trade in and movements of animals, except for slaughter and provided that the healthcertificate includes an indication that the holding is suspected of being infected by trichinellosis;­ provided that the meat and parts of trichinae­infested animals do not come into contact with humansand animals, and shall be harmlessly destroyed;­ instituted the compulsory examination for trichinae of all on­farm slaughtered animals;­ carried out the DDD and other measures in order to sanitise the infected holding.Measures shall be instituted at the infected holding as long as the final DDD measures have not beencarried out.Meat of the trichinae­infested animals shall be assessed as unfit for human consumption.

Notification system in place

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In case of disease, the veterinary organisation must notify the Regional Office of VARS, within thearea of which the disease has been diagnosed. The report on the occurrence of disease is to besubmitted on a monthly basis by the tenth day in a month for the previous month.The authorised laboratory submits the diagnostic test results to the relevant Regional Office of VARS,and to the consigner of samples.Once a month and no later than the 20th day in the month, the authorised laboratories and RegionalOffices of VARS must report on the diagnostic test results to the Office for Contagious AnimalDiseases within VARS. The Main Office of VARS collects the results of ante­ and post­mortem examinations conducted bythe official veterinarians, and applies them in relation to the diagnoses of diseases communicable toman.Where a case of disease is established, the data on the case are reported as soon as possible to theveterinary organisation, duly licensed in accordance with the act governing the veterinary sector,which is supervising the herd of origin of the affected animal.VARS submits to the Commission the data on certain diseases and cases detected, in particular thosecommunicable to man.This method of reporting is carried out in accordance with the provisions of the Rules on contagiousanimal diseases (applicable since 2002), and the reporting as such has been compulsory since 1996.

Results of the investigation including description of the positive cases and the verificationof the Trichinella species

In 2006, no case of trichinellosis in porcine animals was confirmed.

National evaluation of the recent situation, the trends and sources of infection

The last case of trichinellosis was confirmed in 1989. According to data, the positive animal was notof Slovenian origin.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

In Slovenia, taking into account the findings in porcine animals, the possibility of transmission of thedisease to humans is negligible.

B. Trichinella in horses

Monitoring system

Sampling strategy

VARSThe disease, or the larval stage of the agent of disease, is monitored within the scope ofcompulsory veterinary post­mortem examination of animals at slaughter.Systematic examinations for trichinae of the fresh meat of equidae are carried out atslaughterhouses. Epidemiological unit is the animal.

Frequency of the sampling

Examination is carried out on all equidae slaughtered at the registered slaughterhouses.

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Type of specimen taken

Fresh meat: preferable lingual or jaw muscle, otherwise diaphragm, as appropriate.

Methods of sampling (description of sampling techniques)

In accordance with a reference detection method (artificial digestion of a pooled sample in amagnetic stirrer) or trichinoscopy.

Case definition

The disease shall be considered officially confirmed by identifying the agent of disease; in theopposite case it shall be considered that the disease has officially been ruled out.Positive animal – animal where Trichinella spp. has been detected.

Diagnostic/ analytical methods used

­ the magnetic stirrer method for pooled sample digestion­ trichinoscopic examination

Results of the investigation including the origin of the positive animals

In 2006, no case of trichinellosis in equidae was confirmed

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of holdings, establishments, transporters, collection centres anddealers, who are subjected to veterinary checks ­ Identified and registered animals­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming from holdings withan unverified or suspect epizootiological situation­ Holder of a tourist farm activity shall at least 48 hours prior to slaughtering porcine animalsnotify an official veterinarian of the relevant Regional Office of VARS, who shall carry out theante­mortem examination of animals prior to slaughter and a post­mortem examination of themeat upon slaughter. Holder of activity shall provide for the examination of porcine meat forthe presence of trichinae.­ Where the meat is intended for placing on the market it shall be ensured that the fresh meat, incase it has not been examined for trichinae, is subjected to freezing process.­ In case of a suspected presence of disease, the disease shall be confirmed or ruled out.­ Measures for the detection, prevention and suppression of disease.

Measures in case of the positive findings or single cases

At the infected holding there shall be:­ instituted an epizootiological investigation;­ provided and maintained the required conditions of hygiene in the facilities;­ banned the trade in and movements of animals, except for slaughter and provided that the health

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certificate includes an indication that the holding is suspected of being infected by trichinellosis;­ provided that the meat and parts of trichinae­infested animals do not come into contact with humansand animals, and shall be harmlessly destroyed;­ instituted the compulsory examination for trichinae of all on­farm slaughtered animals;­ carried out the DDD and other measures in order to sanitise the infected holding.Measures shall be instituted at the infected holding as long as the final DDD measures have not beencarried out.Meat of the trichinae­infested animals shall be assessed as unfit for human consumption.

Notification system in place

In case of disease, the veterinary organisation must notify the Regional Office of VARS, within thearea of which the disease has been diagnosed. The report on the occurrence of disease is to besubmitted on a monthly basis by the tenth day in a month for the previous month.The authorised laboratory submits the diagnostic test results to the relevant Regional Office of VARS,and to the consigner of samples.Once a month and no later than the 20th day in the month, the authorised laboratories and RegionalOffices of VARS must report on the diagnostic test results to the Office for Contagious AnimalDiseases within VARS. The Main Office of VARS collects the results of ante­ and post­mortem examinations conducted bythe official veterinarians, and applies them in relation to the diagnoses of diseases communicable toman.Where a case of disease is established, the data on the case are reported as soon as possible to theveterinary organisation, duly licensed in accordance with the act governing the veterinary sector,which is supervising the herd of origin of the affected animal.VARS submits to the Commission the data on certain diseases and cases detected, in particular thosecommunicable to man.This method of reporting is carried out in accordance with the provisions of the Rules on contagiousanimal diseases (applicable since 2002), and the reporting as such has been compulsory since 1996.

National evaluation of the recent situation, the trends and sources of infection

In the past 16 years in Slovenia, no case of trichinellosis in equidae has been confirmed.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

In Slovenia, taking into account the findings in equidae, the possibility of transmission of the diseaseto humans is negligible.

C. Trichinella spp., unspecified in animal ­ Wild animals

Monitoring system

Sampling strategy

VARSThe disease, or the larval stage of the agent of disease, is monitored within the scope ofcompulsory veterinary post­mortem examination of killed wild game.

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Frequency of the sampling

Compulsory is the examination of wild boars and other animals, which may be carriers oftrichinae and the meat whereof is intended for public consumption.

Type of specimen taken

Fresh meat: diaphragm, lingual muscle, jaw muscle, abdominal muscles or front leg muscles, asappropriate.

Methods of sampling (description of sampling techniques)

In accordance with a reference detection method (artificial digestion of a pooled sample with amagnetic stirrer) or trichinoscopy.

Case definition

The disease shall be considered officially confirmed by identifying the agent of disease; in theopposite case it shall be considered that the disease has officially been ruled out. Positiveanimal ­ animal where Trichinella spp. has been detected.

Diagnostic/ analytical methods used

­ the magnetic stirrer method for pooled sample digestion­ trichinoscopic examination

Control program/ mechanisms

The control program/ strategies in place

National control programme is carried out in accordance with the national legislation, on thebasis of the Rules on examination for trichinae and meat freezing procedure in order to destroytrichinae, and the Rules onconditions for the collection of killed wild game, veterinary inspection, production of meat andplacing on the market of the meat of killed wild game. The control programme envisages interalia as follows:Wild game or wild game meat may be placed on the market only after the killed animals havevisually been inspected by the official veterinarian and where the meat has been obtained fromwild game that has been subjected to a post­mortem examination (compulsory examination fortrichinae) carried out by an official veterinarian, or by a hunter acting as the veterinary auxiliaryand supervised by the official veterinarian. In case of a suspected presence of disease, thedisease shall be confirmed or ruled out. VARS shall monitor the possible detection ofcontagious diseases in the individual hunting grounds. In case of detecting a contagious disease,measures appropriate to thetype of disease shall be taken.

Measures in case of the positive findings or single cases

Meat of the trichinae­infested animals shall be assessed as unfit for human consumption.

Notification system in place

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Where a zoonosis is detected in wild game, the official veterinarian must notify thereof the relevantRegional Office of VARS that is supervising the hunting ground of killing the particular wild animal,and that Regional Office must take the appropriate measures asprescribed.

Results of the investigation including the origin of the positive animals

In 2006, one case of trichinellosis in wild boar was confirmed.

National evaluation of the recent situation, the trends and sources of infection

In 1998, a single positive case was detected in a wild animal. No positive cases were detected in theperiod 1999­2003. In 2004, trichinellosis was detected in one wild boar, the same as in 2006.In 2005, no positive cases were detected.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

In Slovenia, taking into account the findings in animals, the possibility of transmission of the diseaseto humans is negligible.

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Table Trichinella in animals

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Trichinella sp

p.

T. spiralis

Trichinella sp

p., unspecified

T. britovi

Pigs ­­ at slaughterhouse ­Surveillance (officialsampling)

­ VARS animal 428007 0

­ Surveillance (officialsampling at tourist farm)

­ VARS animal 545 0

Solipeds, domestic ­horses ­­ at slaughterhouse ­Surveillance (officialsampling)

­ VARS animal 1497 0

Wild boars ­ ­ ­wild ­­ at game handlingestablishment ­ Surveillance(official sampling)

­ VARS animal 475 1 0 0 1

farmed ­­ at slaughterhouse ­Surveillance (officialsampling)

­ VARS animal 1 0

Bears ­wild ­ ­ ­­ at game handlingestablishment ­ Surveillance(official sampling)

­ VARS animal 56 0

Deer ­ ­ ­farmed ­ ­ ­­ at slaughterhouse ­Surveillance (officialsampling)

­ VARS animal 1 0

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2.9. ECHINOCOCCOSIS

2.9.1. General evaluation of the national situation

A. Echinococcus spp. general evaluation

History of the disease and/ or infection in the country

According to notifications it is a rare disease in Slovenia.From 1990 to 2006 from 0 to 8 cases yearly have been reported. Most of cases in last years were imported from Balkan countries.AnimalsHydatid cysts are detected from time to time by the compulsory post­mortem examinations atslaughterhouses.

National evaluation of the recent situation, the trends and sources of infection

A rare zoonosis. Infections are mostly imported. In 2005 8 cases and in 2006 three cases were notified(Incidence 0,15 / 100 000 inhabitants).

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Infections are mostly imported.

Recent actions taken to control the zoonoses

Notification system for human cases, identification of source of infection.

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2.9.2. Echinococcosis in humans

A. Echinococcus spp. in humans

Reporting system in place for the human cases

Human cases are notifiable by national Law on Infectious Diseases (Official Gazette 69/ 95). Medicaldoctors, laboratories are obliged to notify cases on daily basis to local institutes of public health. Localinstitutes of public health notify disease to Institute of Public Health of R. Slovenia. Notification since1977.

Case definition

According to definition of commission of the EU communities.

Diagnostic/ analytical methods used

Serology (ELISA etc);ultrasonography,Rtg , CT, MRI ..

Notification system in place

Human cases are notifiable by national Law on Infectious Diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia. Notification since 1977.

History of the disease and/ or infection in the country

According to notifications it is a rare disease in Slovenia.From 1990 to 2006 from 0 to 8 cases yearly have been reported. Most of cases in last years were imported from Balkan countries.AnimalsHydatid cysts are detected from time to time by the compulsory ante­ and post­mortem examinationsat slaughterhouses.

Results of the investigation

In 2005 8 cases have been reported, in 2006 three.

National evaluation of the recent situation, the trends and sources of infection

A rare disease. Most infections are imported.

Relevance as zoonotic disease

Currently not important.

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Table Echinococcus in humans ­ Species/ serotype distribution

Cases

Cases In

c.Autochthon cases

Autochthon Inc.

Imported cases

Imported In

c.

Echinococcus

30.15

00

00

E. granulosus

E. multilocularis

Echinococcus sp

p.3

0.15

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Table Echinococcus in humans ­ Age distribution

E. granulosus

E. m

ultilocularis

Echinococcus spp.

Age Distribution

All

MF

All

MF

All

MF

<1 year

00

0

1 to 4 years

00

0

5 to 14 years

00

0

15 to 24 years

00

0

25 to 44 years

11

0

45 to 64 years

11

0

65 years and older

10

1

Age unknown

Total :

0 0

0 0

0 0

3 2

1

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2.9.3. Echinococcus in animals

A. E. granulosus in animal

Monitoring system

Sampling strategy

VARSMonitored are all slaughter animals and wild game intended for human consumption, andexamined by the official veterinarians at slaughterhouses or wild game processing houseswithin the scope of the compulsory veterinary post­mortem examination.

Frequency of the sampling

Post­mortem examination of all animals and/ or meat and organs upon slaughter or killing.

Type of specimen taken

Organs/ tissues: Hydatic cysts

Methods of sampling (description of sampling techniques)

Visual examination of the slaughtered/ killed animal and its organs, and palpation of the liver.

Case definition

Specific structures in the hydatid cysts must be observed using laboratory microscopy, or thepresence of characteristic antibodies must be determined by serology.

Diagnostic/ analytical methods used

Other: Macroscopic (visual) examination of organs and laboratory microscopic parasitologicalidentification of the agent.

Other preventive measures than vaccination in place

Persons, who in carrying out a registered activity of breeding or production come into direct contactwith animals, foodstuffs, raw materials, products or waste, must have thorough knowledge incontagious animal diseases, the prevention thereof and transmissibility to man, and in the regulationsgoverning the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GHP, and record keeping.Systematic dehelminthisation of dogs along with anti­rabies vaccination.

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of holdings, establishments, transporters, collection centres anddealers, who are subjected to veterinary checks ­ Identified and registered animals

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­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming from holdings withan unverified or suspect epizootiological situation­ The meat and/ or wild game may be placed on the market after the slaughtered/ killed animalshave visually been inspected by the official veterinarian, or by a hunter acting as the veterinaryauxiliary and supervised by the official veterinarian.­ Measures for the detection, prevention and suppression of the disease.

Measures in case of the positive findings or single cases

Harmless disposal of hydatid cysts. In the areas, where the disease is enzootic, double dehelminthisation of dogs.

Notification system in place

In case of disease, the veterinary organisation must notify the Regional Office of VARS, within thearea of which the disease has been diagnosed. The report on the occurrence of disease is to besubmitted on a monthly basis by the tenth day in a month for the previous month.The authorised laboratory submits the diagnostic test results to the relevant Regional Office of VARS,and to the consigner of samples.Once a month and no later than the 20th day in the month, the authorised laboratories and RegionalOffices of VARS must report on the diagnostic test results to the Office for Contagious AnimalDiseases within VARS. The Main Office of VARS collects the results of ante­ and post­mortem examinations conducted bythe official veterinarians, and applies them in relation to the diagnoses of diseases communicable toman.Where a case of the disease is detected, data on the case are promptly communicated to a veterinaryorganisation, which is holding a concession in accordance with the Act governing the veterinarysector, and which is responsible for control of the herd of origin of affected animal.VARS submits to the Commission the data on certain diseases and cases detected, in particular thosecommunicable to man.

Results of the investigation

In 2006, Echinococcus granulosus was detected in bovine animals in 9 cases (0,006%) of 140430bovine animals tested, and in porcine animals in 14 cases (0,003%) of 428552 porcine animals tested. No E. granulosus was detected in the slaughtered small ruminants neither in slaughtered horses.E. granulosus was also not confirmed in any of the wild animals, whose internal organs wereinspected by official veterinarians in the wild game handling establishments.

National evaluation of the recent situation, the trends and sources of infection

In 2006, the number of cases of Echinococcosis in bovine animals remained approximately the sameas in 2005. In 2006, the number of cases of Echinococcosis in porcine animals decreasedconsiderably, and therefore, the situation is assessed as favourable.

B. Echinococcus spp., unspecified in animal

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Monitoring system

Sampling strategy

VARSMonitored are all slaughter animals and wild game intended for human consumption, andexamined by the official veterinarians at slaughterhouses or wild game processing houseswithin the scope of the compulsory veterinary post­mortem examination.

Frequency of the sampling

Post­mortem examination of all animals and/ or meat and organs upon slaughter or killing.

Type of specimen taken

Other: Visual examination of the slaughtered/ killed animal and its organs, and palpation of theliver

Case definition

Detection of hydatid cysts in the liver, the lungs and some other organs of the slaughtered,killed or dead animals (porcines, small ruminants, bovines, equidae, and some wild gamespecies).

Diagnostic/ analytical methods used

Other: Pathoanatomic examination, visual examination and palpation of organs

Other preventive measures than vaccination in place

Persons, who in carrying out a registered activity of breeding or production come into direct contactwith animals, foodstuffs, raw materials, products or waste, must have thorough knowledge incontagious animal diseases, the prevention thereof and transmissibility to man, and in the regulationsgoverning the protection against contagious diseases.In accordance with legislation, the business operator shall provide for conditions of hygiene inprimary production ­ GHP, and record keeping.Systematic dehelminthisation of dogs along with anti­rabies vaccination.

Control program/ mechanisms

The control program/ strategies in place

­ Registration and/ or approval of holdings, establishments, transporters, collection centres anddealers, who are subjected to veterinary checks ­ Identified and registered animals­ Regular official veterinary checks on holdings­ Movements of animals accompanied by prescribed documents­ Veterinary referral form to accompany sick animals and animals coming from holdings withan unverified or suspect epizootiological situation­ The meat and/ or wild game may be placed on the market after the slaughtered/ killed animalshave visually been inspected by the official veterinarian, or by a hunter acting as the veterinaryauxiliary and supervised by the official veterinarian.

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­ Measures for the detection, prevention and suppression of the disease.

Measures in case of the positive findings or single cases

Harmless disposal of hydatid cysts. In the areas, where the disease is enzootic, double dehelminthisation of dogs.

Notification system in place

In case of disease, the veterinary organisation must notify the Regional Office of VARS, within thearea of which the disease has been diagnosed. The report on the occurrence of disease is to besubmitted on a monthly basis by the tenth day in a month for the previous month.The authorised laboratory submits the diagnostic test results to the relevant Regional Office of VARS,and to the consigner of samples.Once a month and no later than the 20th day in the month, the authorised laboratories and RegionalOffices of VARS must report on the diagnostic test results to the Office for Contagious AnimalDiseases within VARS. The Main Office of VARS collects the results of ante­ and post­mortem examinations conducted bythe official veterinarians, and applies them in relation to the diagnoses of diseases communicable toman.Where a case of the disease is detected, data on the case are promptly communicated to a veterinaryorganisation, which is holding a concession in accordance with the Act governing the veterinarysector, and which is responsible for control of the herd of origin of affected animal.VARS submits to the Commission the data on certain diseases and cases detected, in particular thosecommunicable to man.

Results of the investigation

In 2006, hydatid cysts was detected in 15 bovine animals (0,011 %) of 140430 bovine animals tested,and in 54 porcine animals (0.013 %) of 428552 porcine animals tested. No hydatic cysts were detected in the slaughtered small ruminants neither in the slaughtered horses.

National evaluation of the recent situation, the trends and sources of infection

Hydatid cysts are detected from time to time by the compulsatory post­mortem examinations atslaughterhouses and wild game processing houses.

Relevance of the findings in animals to findings in foodstuffs and to human cases (as asource of infection)

The percentage of positive cases in animal population is rather low, i.e. less than 0.5 %. Taking intoaccount the rarity of cases in animal population it may be concluded that human population in generalis not at risk.

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Table Echinococcus in animals

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Echinococcus spp.

E. granulosus

E. m

ultilocularis

Echinococcus spp., unspecified

Cattle (bovine animals) ­ VARS animal 140430 9 9 0 0

Sheep ­ VARS animal 10263 0

Goats ­ VARS animal 315 0

Pigs ­ VARS animal 428552 14 14 0 0

Solipeds, domestic ­ VARS animal 1497 0

Wild boars ­ ­ ­wild ­ ­ ­­ at game handlingestablishment ­ Surveillance(official sampling)

­ VARS animal 112 0

farmed ­ ­ ­­ at slaughterhouse ­Surveillance (officialsampling)

­ VARS animal 1 0

Bears ­ ­ ­wild ­ ­ ­­ at game handlingestablishment ­ Surveillance(official sampling)

­ VARS animal 10 0

Deer ­ ­ ­wild ­ ­ ­roe deer ­ ­ ­­ at game handlingestablishment ­Surveillance (officialsampling)

­ VARS animal 65 0

red deer ­ ­ ­­ at game handlingestablishment ­Surveillance (officialsampling)

­ VARS animal 94 0

fallow deer ­ ­ ­­ at game handlingestablishment ­Surveillance (officialsampling)

­ VARS animal 21 0

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farmed ­ ­ ­red deer ­ ­ ­­ at slaughterhouse ­Surveillance (officialsampling)

­ VARS animal 1 0

Mouflons ­ ­ ­wild ­ ­ ­­ at game handlingestablishment ­ Surveillance(official sampling)

­ VARS animal 64 0

Alpine chamois ­ ­ ­wild ­ ­ ­­ at game handlingestablishment ­ Surveillance(official sampling)

­ VARS animal 14 0

Footnote

Number of sheeps monitored:10.224 ­ official sampling at slaughterhouse39 ­ official sampling at tourist farmNumber of pigs monitored:428.007 ­ official sampling at slaughterhouse545 ­ official sampling at tourist farm

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2.10. TOXOPLASMOSIS

2.10.1. General evaluation of the national situation

A. Toxoplasmosis general evaluation

History of the disease and/ or infection in the country

Human cases are notifiable by national Law on Infectious Diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia. Notification since 1977.

National evaluation of the recent situation, the trends and sources of infection

The average yearly number of notifications of human cases from 2002 to 2006 was 27 and variedfrom 22 to 38 cases. (During that period average yearly incidence was 1,36 / 100 000 inhabitants andvariied from 1,1 to 1,9 / 100 000 inhabitants).

Recent actions taken to control the zoonoses

Notification system, screening of pregnant women on routine basis.

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2.10.2. Toxoplasmosis in humans

A. Toxoplasmosis in humans

Reporting system in place for the human cases

Human cases are notifiable by national Law on Infectious Diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia. Notification since 1977.

Case definition

According to comission of EU.

Diagnostic/ analytical methods used

Toxoplasma is identificated in laboratory of Medical Faculty in Ljubljana, in Laboratory of Instituteof Transf, and some labs in Institutes of Public Health.Methods used are:Serology: detection of IgG, IgM, IgA with EIA (Abott); avidity of Ig (Biorat Platelia);isolation;PCR.

Notification system in place

Human cases are notifiable by national Law on Infectious Diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia. Notification since 1977.

History of the disease and/ or infection in the country

Number of notifications decreases.

Relevance as zoonotic disease

Important for some population groups­ on example pregnant women. Screening during pregnancy isdone routinely.

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Table Toxoplasm

a in hum

ans ­ Species/ serotype distribution

Cases

Cases In

c.

Toxoplasm

a24

1.2

T. gondii

241.2

Toxoplasma spp.

Congenital cases

20.1

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Table Toxoplasm

a in hum

ans ­ Age distribution

T. gondii

Toxoplasm

a spp.

Age Distribution

All

MF

All

MF

<1 year

31

2

1 to 4 years

00

0

5 to 14 years

00

0

15 to 24 years

92

7

25 to 44 years

114

7

45 to 64 years

10

1

65 years and older

00

0

Age unknown

Total :

24

7 17

0 0

0

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2.10.3. Toxoplasma in animals

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2.11. RABIES

2.11.1. General evaluation of the national situation

A. Rabies general evaluation

History of the disease and/ or infection in the country

From 1946 to 1950 13 human rabies cases­deaths were recorded. Since 1950 no human cases havebeen notified in Slovenia. Dog­mediated rabies was eradicated soon after World War II, when compulsory vaccination of dogsagainst rabies came into force (1947). Since that time all dogs in Slovenia are compulsorily vaccinatedagainst rabies.Wildlife­mediated rabies has been present since 1973, when the first rabid animal (red fox) wasdetected in the NW of Slovenia. It had progressively spread trough the territory of the municipalitiesof Murska Sobota and Lendava, but it has never crossed the natural barrier of the Mura River.The second wave of sylvatic rabies reached Slovenia in 1979 from Austria. From there it has beenspread throughout the country nd has persisted until the present.Due to the inconvenient epizootiological situation regarding rabies in the 1980­ies, the VeterinaryAdministration decided to implement the oral vaccination of foxes against rabies. In 1988, when thepilot project of the manual distribution of baits (so­called Tübingen Model with the SAD type) wasstarted, vaccination was conducted in a small part of Slovenia only. Thereafter, two vaccinationcampaigns (in spring and autumn) were performed as the strategy of pushing rabies from west to east.At that time, 40,000 to 60,000 baits were distributed in each campaign in a rate of 16 to 20 baits perkm2. In a few years that followed, the whole territory of Slovenia was covered three times. It wasfound that if only a certain region was covered at one time, the success rate was poor. And this was the reason that in 1995, we started with a new strategy to combat rabies. The aircraftdistribution of baits has been perfomed twice per year – spring and autumn. The GPS was used tosupport bait distribution and is still used today as a prevailing strategy. Each year, 640,000 baits weredeposited (320,000 per campaign, 20 baits/ km2). The follow up investigations such as anti­body andmarker investigations, have been carried out. Specific software has been developed in order to analysedata received from the computer (connected to the GPS). The results of new strategy were veryencouraging. The number of rabies cases decreased from 1089 (996 foxes) in 1995 to only 6 cases (5foxes) in 1999. All cases were detected near the border with Croatia.In 2000, the number of cases increased again. Because of new tax policy the OVF budget decreasedand at the same time there was a deteriorating situation regarding rabies in South – Easternneighbourhood. Therefore, the distribution pattern was changed again.

National evaluation of the recent situation, the trends and sources of infection

No human cases were recorded after 1950.In 2004, only 2 positive animals (foxes) were detected. Both cases were on the SE border. In 2005, two rabies cases on the border of vaccination area were detected. Emergency vaccination in30 km radius around this two outbreaks and taking into account the natural barierrs was carried out.With emergency vaccination we tried to avoid the spread of the disease outside the vaccionation area. The third case was detected in May in municipality Ilirska Bistrica on the border region with Croatia.

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In 2006, 1896 (1.645 foxes) animals were tested on rabies. Two rabid foxes were detected near theborder with Croatia.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Epizootic situation improved since introduction of vaccination of wild animals; no human cases wererecorded after 1950.There is possibility of importation of human cases in spite of fact, that preexposure vaccination isavailable for foreign travellers.

Recent actions taken to control the zoonoses

Ongoing oral vaccination of foxes twice per year.

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2.11.2. Rabies in humans

A. Rabies in humans

Reporting system in place for the human cases

Rabies cases are notifiable by national Law on Infectious Diseases. Medical doctors, laboratories areobliged to notify cases on daily basis to local institutes of public health. Local institutes of publichealth notify disease to Institute of Public Health of R. Slovenia.No human cases in Slovenia since 1950.

Case definition

According to definition of commission of the EU communities.

Diagnostic/ analytical methods used

Virologic laboratory of Veterinary Faculty in Ljubljana uses methods:serology (neutralisation test);isolation on cell cultures, also mouse neuroblasts;RT­PCR;direct imunofluorescent test.

Notification system in place

Rabies cases are notifiable by national Law on Infectious Diseases. Medical doctors are obliged tonotify cases on daily basis to local institutes of public health. Local institutes of public health notifydisease to Institute of Public Health of R. Slovenia. Notification since second World War.

History of the disease and/ or infection in the country

From 1946 to 1950 13 human rabies cases­deaths were recorded. Since 1950 no human cases havebeen notified in Slovenia. There were no human and animal cases from 1950 to 1973. From 1973 to 1988 rabies spread among wild animals in all regions of Slovenia. In 1988 vaccinationcampaign of wild animals started and continued in 1995 and last years.

Results of the investigation

No human cases were recorded after 1950. Epizootic situation improved since the start of vaccination of wild animals.

National evaluation of the recent situation, the trends and sources of infection

Epizootic situation improved since introduction of vaccination of wild animals; no human cases wererecorded after 1950.(There is possibility of importation of human cases in spite of fact, that preexposure vaccination isavailable for foreign travellers).

Relevance as zoonotic disease

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In Slovenia postexposure prophylaxis of injured persons after bite or injury caused by unknown wildor domestic animal is still obligatory by law.Preexposure prophylaxis is obligatory by law as well for persons, potentially exposed to infectionduring work.Preexposure prophylaxis is also available for foreign travellers.Surveillance of epizootic situation goes on.

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2.11.3. Lyssavirus (rabies) in animals

A. Rabies in dogs

Vaccination policy

Compulsorily vaccination of all dogs older than 3 months.

Additional information

Dog­mediated rabies was eradicated soon after World War II, when compulsory vaccination of dogsagainst rabies came into force (1947). Since that time all dogs in Slovenia are compulsorily vaccinatedagainst rabies.

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Table Rabies in animals

­ ­

Source of information

Sampling unit

Units tested

Total units positive for Lyssavirus (rabies)

unspecified Lyssavirus

European Bat Lyssavirus ­ unspecified

classical rabies virus (genotype 1)

Cattle (bovine animals) ­ VARS animal 16 0

Sheep ­ VARS animal 12 0

Goats ­ VARS animal 1 0

Pigs ­ VARS animal 0 0

Solipeds, domestic ­ VARS animal 0 0

Dogs ­ VARS animal 63 0

Cats ­ VARS animal 65 0

Foxes ­ ­ ­wild ­ VARS animal 1645 2 0 0 2

Wolves ­ ­ ­wild ­ VARS animal 11 0

Badgers ­ ­ ­wild ­ VARS animal 20 0

Marten ­ ­ ­wild ­ VARS animal 43 0

Deer ­ VARS animal 13 0

wild ­ ­ ­roe deer ­ VARS animal 13 0

Rats ­ ­ ­wild ­ VARS animal 2 0

Hamsters ­ ­ ­pet animals ­ VARS animal 1 0

Bears ­ ­ ­wild ­ VARS animal 1 0

Polecats ­ ­ ­wild ­ VARS animal 1 0

Mice ­ ­ ­wild ­ VARS animal 2 0

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2.12. Q­FEVER

2.12.1. General evaluation of the national situation

2.12.2. Coxiella (Q­fever) in animals

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3. INFORMATION ON SPECIFIC INDICATORS OF ANTIMICROBIALRESISTANCE

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3.1. ESCHERICHIA COLI, NON­PATHOGENIC

3.1.1. General evaluation of the national situation

A. Escherichia coli general evaluation

History of the disease and/ or infection in the country

According to Law on infectious diseases (Official Gazette 69/ 95) E.coli infections are notifiable.Doctors and laboratories are obliged to notify them in three days after diagnosis. The number of allE.coli infections in 2005 was 117, 22 from them were identified as other E.coli infections. In 2006there were 121 notifications, among those 25 were diagnosed as other E.coli infections. Theproportion or incidence of nonpathogenic E.coli is not clear, because most E.coli notifications do nothave serotype data, may be nonpathogenic E.coli are diganosed as "concomitant" bacteria and areprobably not notified at all.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Non­pathogenic E. coli (100 strains, of which 13 from cattle, 66 from poultry (Gallus gallus), 5 frompigs, 4 from turkeys, 8 from dogs and 4 from zoo moose) were tested in indicators of antimicrobialresistance. Also 21 strains of E. coli O:157 from animals and food were included. The same battery of20 antimicrobials as for Salmonella was used.Of poultry strains only 9% of strains were fully susceptible, while 30% of strains were resistant tomore than 4 antimicrobials. Of cattle strains 61% of strains were resistant to 1 antimicribial, and 23%of strains were fully susceptible. From turkeys we had only 4 strains, which is not enough to draw arelevant conclusion. Strains resistant to more than one antimicrobial were found. Similar situation isin pigs and in zoo animals. Although a small number of strains from dogs were tested, the results arenot encouraging. Two strains resistant to 8 antimicrobials were found. Due to close contact betweendogs and their owners and the rest of the family including children, this source of multiresitant strainsand the possible transfer of resistant determinants to other bacterial species (especially enterobacteriaincluding Salmonella) this source of risk should not be neglected.

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3.1.2. Antimicrobial resistance in Escherichia coli, non­pathogenic isolates

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Table Antimicrobial su

sceptib

ility testing of E. coli in Pigs ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­Pigs

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

5

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

52

22

1

Amphenicols

Chloram

phenicol

50

12

2

Florfenicol

50

12

2

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

50

11

12

Ceftiofur

50

11

12

Ceftriaxon

50

11

12

Fluoroquinolones

Ciprofloxacin

50

11

11

1

Enrofloxacin

50

11

3

Quinolones

Nalidixic acid

51

11

12

Sulfonamides

Sulfonamide

51

11

21

Trimethoprim

51

11

21

Aminoglycosides

Streptom

ycin

52

21

2

Gentamicin

51

11

12

Neomycin

50

13

1

Kanam

ycin

51

11

12

Spectinom

ycin

51

11

12

Penicillins

Amoxicillin

52

11

12

Amoxicillin / Clavulanic acid

52

11

12

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Ampicillin

53

32

Trimethoprim + su

lfonamides

51

12

11

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Table Antimicrobial su

sceptib

ility testing of E. coli in Moose ­ zoo animal ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­Moose ­ zoo animal

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

4

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

42

21

1

Amphenicols

Chloram

phenicol

41

11

11

Florfenicol

40

11

2

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

40

4

Ceftiofur

40

12

1

Ceftriaxon

40

12

1

Fluoroquinolones

Ciprofloxacin

41

11

2

Enrofloxacin

41

11

11

Quinolones

Nalidixic acid

41

11

11

Sulfonamides

Sulfonamide

42

21

1

Trimethoprim

41

11

11

Aminoglycosides

Streptom

ycin

42

21

1

Gentamicin

40

31

Neomycin

41

12

1

Kanam

ycin

41

12

1

Spectinom

ycin

40

11

11

Penicillins

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Amoxicillin

42

21

1

Amoxicillin / Clavulanic acid

40

12

1

Ampicillin

42

21

1

Trimethoprim + su

lfonamides

41

11

11

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Table Antimicrobial su

sceptib

ility testing of E. coli in Cattle (bovine animals) ­ quantitative data

[Diffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­Cattle (bovine animals)

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

13

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

132

22

61

2

Amphenicols

Chloram

phenicol

131

11

41

42

Florfenicol

130

13

24

11

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

130

13

44

1

Ceftiofur

130

11

12

41

3

Ceftriaxon

130

25

15

Fluoroquinolones

Ciprofloxacin

130

21

51

31

Enrofloxacin

130

11

52

11

2

Quinolones

Nalidixic acid

131

12

22

22

11

Sulfonamides

Sulfonamide

132

21

22

32

1

Trimethoprim

139

91

11

1

Aminoglycosides

Streptom

ycin

122

24

51

Gentamicin

131

11

33

32

Neomycin

130

11

65

Kanam

ycin

130

11

26

21

Spectinom

ycin

131

15

31

3

Penicillins

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Amoxicillin

130

13

12

42

Amoxicillin / Clavulanic acid

130

17

22

1

Ampicillin

131

11

21

31

22

Trimethoprim + su

lfonamides

130

11

25

31

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Table Antimicrobial su

sceptib

ility testing of E. coli in Dogs ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­Dogs

Isolates out of a monitoring

programme

no

Num

ber of isolates available in

the laboratory

8

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

80

15

11

Amphenicols

Chloram

phenicol

82

22

21

1

Florfenicol

72

23

11

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

81

12

13

1

Ceftiofur

81

11

42

Ceftriaxon

81

12

31

1

Fluoroquinolones

Ciprofloxacin

82

21

21

2

Enrofloxacin

82

21

41

Quinolones

Nalidixic acid

82

21

11

12

Sulfonamides

Sulfonamide

83

31

11

2

Trimethoprim

83

31

11

11

Aminoglycosides

Streptom

ycin

83

34

1

Gentamicin

82

21

31

1

Neomycin

80

14

21

Kanam

ycin

80

22

31

Spectinom

ycin

82

21

31

1

Penicillins

Amoxicillin

81

12

23

Amoxicillin / Clavulanic acid

81

12

21

11

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Ampicillin

83

31

11

11

Trimethoprim + su

lfonamides

82

21

11

11

1

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Table Antimicrobial su

sceptib

ility testing of E. coli in All animals ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­All animals

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

21

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

211

12

16

61

31

Amphenicols

Chloram

phenicol

210

13

25

51

22

Florfenicol

210

21

62

32

21

11

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

210

11

35

47

Ceftiofur

210

21

54

23

22

Ceftriaxon

210

11

43

12

Fluoroquinolones

Ciprofloxacin

210

11

25

17

4

Enrofloxacin

210

33

24

32

22

Quinolones

Nalidixic acid

210

33

44

21

31

Sulfonamides

Sulfonamide

212

21

11

22

27

21

Trimethoprim

211

11

12

12

21

32

14

Aminoglycosides

Streptom

ycin

211

12

47

42

1

Gentamicin

210

16

45

5

Neomycin

210

33

66

21

Kanam

ycin

210

21

13

54

22

1

Spectinom

ycin

210

43

55

31

Penicillins

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Amoxicillin

211

13

18

25

1

Amoxicillin / Clavulanic acid

210

11

57

51

1

Ampicillin

211

13

18

31

21

1

Trimethoprim + su

lfonamides

211

11

12

26

43

1

Footnote

E. coli O

157 from

monitoring of animals and food in veterinary laboratories

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Table Antimicrobial susceptibility testing of E. coli in animals

n = Number of resistant isolates

E. coliCattle(bovineanimals)

Pigs Gallus gallus(fowl)

Turkeys All animals Dogs Moose ­ zooanimal

Isolates out of a monitoringprogramme

yes yes yes yes yes no no

Number of isolatesavailable in the laboratory

13 5 66 4 21 8 4

­Antimicrobials: N n N n N n N n N n N n N nTetracyclines

Tetracyclin 13 2 5 2 66 28 4 2 21 1 8 0 4 2Amphenicols

Chloramphenicol 13 1 5 0 66 6 4 0 21 0 8 2 4 1Florfenicol 13 0 5 0 66 2 4 0 21 0 8 2 4 0

CephalosporinsCefotaxim 13 0 5 0 66 1 4 0 21 0 8 1 4 0Ceftiofur 13 0 5 0 66 2 4 0 21 0 8 1 4 0Ceftriaxon 13 0 5 0 66 3 4 0 21 0 8 1 4 0

FluoroquinolonesCiprofloxacin 13 0 5 0 66 16 4 0 21 0 8 2 4 1Enrofloxacin 13 0 5 0 66 17 4 0 21 0 8 2 4 1

QuinolonesNalidixic acid 13 1 5 1 66 41 4 0 21 0 8 2 4 1

SulfonamidesSulfonamide 13 2 5 1 66 19 4 0 21 2 8 3 4 2

Trimethoprim 13 9 5 1 66 31 4 2 21 1 8 3 4 1

AminoglycosidesStreptomycin 13 2 5 2 66 20 4 0 21 1 8 3 4 2Gentamicin 13 1 5 1 66 10 4 0 21 0 8 2 4 0Neomycin 13 0 5 0 66 3 4 0 21 0 8 0 4 1Kanamycin 13 0 5 1 66 4 4 0 21 0 8 0 4 1Spectinomycin 13 1 5 1 66 11 4 0 21 0 8 2 4 0

PenicillinsAmoxicillin 13 0 5 2 66 34 4 0 21 1 8 1 4 2Amoxicillin / Clavulanicacid

13 0 5 2 66 11 4 0 21 0 8 1 4 0

Ampicillin 13 1 5 3 66 41 4 0 21 1 8 3 4 2

Trimethoprim +sulfonamides

13 0 5 1 66 7 4 0 21 1 8 2 4 1

Fully sensitive 13 3 5 2 66 6 4 1 21 19 8 3 4 2

Resistant to 1 antimicrobial 13 8 66 12 4 1 8 1

Resistant to 2antimicrobials

66 12 4 2 8 2

Resistant to 3antimicrobials

5 2 66 12 21 1

Resistant to 4antimicrobials

13 1 66 4 21 1

Resistant to >4antimicrobials

13 1 5 1 66 20 8 2 4 2

Footnote

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"All animals" stands for E. coli O:157 from monitoring of animals and food in veterinary laboratories.

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Table Antimicrobial su

sceptib

ility testing of E. coli in Turkeys ­ quantitative data [D

iffusion method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­Turkeys

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

4

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

42

21

1

Amphenicols

Chloram

phenicol

40

11

11

Florfenicol

40

11

2

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

40

12

1

Ceftiofur

40

11

11

Ceftriaxon

40

12

1

Fluoroquinolones

Ciprofloxacin

40

11

11

Enrofloxacin

40

11

11

Quinolones

Nalidixic acid

40

11

11

Sulfonamides

Sulfonamide

40

12

1

Trimethoprim

42

21

1

Aminoglycosides

Streptom

ycin

40

12

1

Gentamicin

40

11

2

Neomycin

40

21

1

Kanam

ycin

40

22

Spectinom

ycin

40

11

2

Penicillins

Amoxicillin

40

11

11

Amoxicillin / Clavulanic acid

40

11

11

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Ampicillin

40

12

1

Trimethoprim + su

lfonamides

40

13

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Table Antimicrobial su

sceptib

ility testing of E. coli in Gallus gallus (fowl) ­ quantitative data [D

iffusion

method]

Num

ber of resistant isolates (n) and num

ber of isolates with

the concentration µl/ m

l) or zone (m

m) of inhibition equal to

­E. coli

­Gallus g

allus (fowl)

Isolates out of a monitoring

programme

yes

Num

ber of isolates available in

the laboratory

66

­ Antimicrobials:

Nn

<=6

78

910

1112

1314

1516

1718

1920

2122

2324

2526

2728

2930

3132

3334

>=35

Tetracyclines

Tetracyclin

6628

281

133

32

82

41

1

Amphenicols

Chloram

phenicol

666

51

61

73

912

65

71

21

Florfenicol

662

11

43

126

54

93

72

62

1

Cephalosporins

3rd generation cephalosporins

0

Cefotaxim

661

11

21

41

181

112

1410

Ceftiofur

662

23

11

23

76

163

146

2

Ceftriaxon

663

31

32

310

212

210

39

6

Fluoroquinolones

Ciprofloxacin

6816

64

21

21

12

33

33

33

36

82

64

2

Enrofloxacin

6617

112

11

23

36

15

13

22

68

14

13

Quinolones

Nalidixic acid

6641

401

24

47

43

1

Sulfonamides

Sulfonamide

6619

191

31

58

38

56

13

11

1

Trimethoprim

6631

301

11

11

11

15

36

65

11

1

Aminoglycosides

Streptom

ycin

6620

191

722

103

21

1

Gentamicin

6610

51

11

212

1113

125

21

Neomycin

663

21

28

2512

93

21

1

Kanam

ycin

664

31

513

2210

73

11

Spectinom

ycin

6611

51

41

24

1718

73

21

1

Penicillins

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Amoxicillin

6634

221

22

75

73

54

41

11

1

Amoxicillin / Clavulanic acid

6611

71

31

46

97

46

76

41

Ampicillin

6641

401

23

32

48

11

1

Trimethoprim + su

lfonamides

667

61

11

11

11

63

193

122

71

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Table Antimicrobial susceptibility testing of E. coli in humans

n = Number of resistant isolates

E. colihumans

Isolates out of a monitoringprogramme Number of isolatesavailable in the laboratory(1)

2

­Antimicrobials: N nTetracyclines

Tetracyclin 2 0Amphenicols

Chloramphenicol 2 0Fluoroquinolones

Ciprofloxacin 2 0Quinolones

Nalidixic acid 2 0Aminoglycosides

Gentamicin 2 0Kanamycin 2 0Spectinomycin 2 0

PenicillinsAmpicillin 2 0

Trimethoprim +sulfonamides

2 0

(1) : VTEC strains

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Table Breakpoints used for antimicrobial susceptibility testing in Animals

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Escherichia coli,non­pathogenic

Standard forbreakpoint

Breakpoint concentration (microg/ ml) Range tested concentration(microg/ ml)

Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

AmphenicolsChloramphenicol 30 18 12

Florfenicol 30 20 16

TetracyclinesTetracyclin 30 19 14

FluoroquinolonesCiprofloxacin 5 21 15

Enrofloxacin 5 20 16

QuinolonesNalidixic acid 30 19 13

Trimethoprim 5 16 10

SulfonamidesSulfonamide 300 17 12

AminoglycosidesStreptomycin 10 15 11

Gentamicin 10 15 12

Neomycin 30 17 12

Kanamycin 30 18 13

Spectinomycin 100 18 14

Trimethoprim +sulfonamides

25 16 10

CephalosporinsCefotaxim 30 23 14

Ceftiofur 30 20 16

Ceftriaxon 30 21 13

3rd generationcephalosporins

PenicillinsAmoxicillin 10 17 13

Amoxicillin /Clavulanic acid

30 17 13

Ampicillin 10 17 13

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Table Breakpoints used for antimicrobial susceptibility testing in Humans

Test Method Used

­ Disc diffusion

­ Agar dilution

­ Broth dilution

­ E­test

Standards used for testing

­ NCCLS

­Escherichia coli,non­pathogenic

Standard forbreakpoint

Breakpoint concentration (microg/ ml) Range tested concentration(microg/ ml)

Disk content Breakpoint Zone diameter (mm)

Susceptible<=

Intermediate Resistant>

lowest highest microg Susceptible>=

Intermediate Resistant<=

AmphenicolsChloramphenicol 30 18 15 12

Florfenicol TetracyclinesTetracyclin 30 19 16 14

FluoroquinolonesCiprofloxacin 5 21 18 15

Enrofloxacin QuinolonesNalidixic acid 30 19 16 13

Trimethoprim 5 16 13 10

SulfonamidesSulfonamide

AminoglycosidesStreptomycin 10 15 13 11

Gentamicin 10 15 13 12

Neomycin Kanamycin 30 18 16 13

Spectinomycin

Trimethoprim +sulfonamides

CephalosporinsCefotaxim Ceftiofur Ceftriaxon 3rd generationcephalosporins

PenicillinsAmoxicillin Amoxicillin /Clavulanic acid Ampicillin 10 17 15 13

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4. INFORMATION ON SPECIFIC MICROBIOLOGICAL AGENTS

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4.1. HISTAMINE

4.1.1. General evaluation of the national situation

A. Histamine General evaluation

History of the disease and/ or infection in the country

Human cases of microbial food intoxication are notifiable by National Law on infectious diseases(Official Gazette number 69/ 1995).Medical doctors, laboratories are obliged to notify cases to local institutes of public health. Localinstitutes of public health notify disease to Institute of Public Health of R. Slovenia. Histamin intoxication is according to Law on infectiou diseases (Official Gazette number 69/ 1995)not notifiable. (It could be notified as gastroenterocolitis acuta, without identified agent). Mostpatients with symptoms of histamin intoxication, which is not severe, do not seek medical help. Ifthey go to doctor, cases are mostly not notified.Therefore the disease is underreported. From 1980 on to January 2005 less than 15 cases of histamin intoxication were officially recorded inSlovenia. Cases were intoxicated by eating fishes in sandwich, on pizza, noodles with tuna fish and tomatosauce.

National evaluation of the recent situation, the trends and sources of infection

Last case was recorded 2002. The patient ate tunna salad and went ill one hour later. Later there wereno official notifications.

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

The source of infection was mostly canned fish: tuna fish, mackerel.

Recent actions taken to control the hazard

Sampling of food in restaurants, in food shops, education of food workers against: storing fishes, opened canned fish on room temperature; using large amounts of fish instead of opening smaller canns, containing fish;measuring temperature in refrigerators, where fishes are kept etc.

Suggestions to the Community for the actions to be taken

Occasional sampling of canned fish for laboratory evaluation of histamin content?

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4.1.2. Histamine in foodstuffs

A. Histamine in foodstuffs

Monitoring system

Sampling strategy

HIRS has taken samples at the retail level.

Frequency of the sampling

Samples are taken once per year.

Methods of sampling (description of sampling techniques)

Samples are taken randomly from the available lot.

Definition of positive finding

Definition of positive finding as written in the Regulation 2073/ 2005.

Diagnostic/ analytical methods used

HLPC

Preventive measures in place

Regular monitoring.

Control program/ mechanisms

The control program/ strategies in place

Regular monitoring.

Measures in case of the positive findings or single cases

In case of non­compliance with the regulation 2073/ 2005 recall follows.

Notification system in place

All positive samples are evaluated by RASFF unit.

Results of the investigation

HIRS took 10 samples in 9 subunits and none was posititive on presence of histamin.

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Table Histamine in food

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units in non­ conform

ity

<= 100 mg/ kg

>100 ­ <=

200 mg/ kg

>200 ­ <=

400 mg/ kg

> 400 mg/ kg

Fish ­ ­

­

Fishery products from fishspecies associated with a highamount of histidine ­ notenzyme maturated

­ HIRS batch 9* 10 0 10 0 0 0

Footnote

9* ­ number of subunits of the sampleeach weighting 125 ­ 195g.

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4.2. ENTEROBACTER SAKAZAKII

4.2.1. General evaluation of the national situation

A. Enterobacter sakazakii general evaluation

History of the disease and/ or infection in the country

Infections with Enterobacter sakazakii are according to our Law on infectious diseases ( OfficialGazette 69/ 95) not notifiable. Therefore we do not have any offcial notifications.

National evaluation of the recent situation, the trends and sources of infection

Unknown.

Recent actions taken to control the hazard

Law on infectious diseases from 1995 is beeing modified in the moment. Enterobacter sakazakii infections could be added to the list of obligatory notifiable diseases.

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4.2.2. Enterobacter sakazakii in foodstuffs

A. Enterobacter sakazakii in foodstuffs

Monitoring system

Sampling strategy

HIRS is executing monitoring at wholesale level, where samples of different producers aretaken.

Frequency of the sampling

Once per year all samples are taken.

Methods of sampling (description of sampling techniques)

Prepacked baby food is taken randomly from the available part of the consignment.

Definition of positive finding

Presence of E.sakazakii in 25g.

Diagnostic/ analytical methods used

Method according to U. S. Food and Drug Administration, Center for Food Safety andApplied Nutrition, july 2002; Revised August 2002

Preventive measures in place

GMP, GHP, HACCP

Measures in case of the positive findings or single cases

Recall from the market, inspection at the producer.

Notification system in place

All of the positive results are evaluated at the RASFF unit, in 2006 none was positive.

Results of the investigation

None of 10 samples was positive.

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Table Enterobacter sakazakii in food

­ ­

Source of information

Sampling unit

Sample weight

Units tested

Total units positive for Enterobacter sakazakii

Infant formula ­ ­

­

dried ­ HIRS single 25g 10 0

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4.3. STAPHYLOCOCCAL ENTEROTOXINS

4.3.1. General evaluation of the national situation

A. Staphylococcal enterotoxins general evaluation

History of the disease and/ or infection in the country

Human cases of Stapylococcal intoxication are notifiable by National Law on Infectious Diseases(official Gazette number 69/ 1995). Notifiable are sporadic cases and outbreaks as well.Medical doctors are obliged to notify cases on daily basis to local institutes of public health. Localinstitutes of public health notify disease to Institute of Public Health of R. Slovenia. Notificated formore than 30 years.

National evaluation of the recent situation, the trends and sources of infection

From 2000 to 2006 the average number of sporadic notificated cases of staphylococcal food poisoningwas 15 (from 1 to 63) yearly. Staphylococci are the second most frequent bacteria, which cause food intoxication outbreaks inSlovenia (after Salmonella spp). During the same period number of notificated outbreaks varied from zero to 5 yearly (Places ofintoxication were: schools, school camps, restaurants, family outbreaks. In 2006 we notified threeoutbreaks of staphylococcal poisoning. (Two in school camps and one in a restaurant).

Relevance of the findings in animals, feedingstuffs and foodstuffs to human cases (as asource of infection)

Sources of infection from outbreaks are different­from human cariers to milk/ milk products, potatosalad etc.

Recent actions taken to control the hazard

Implementation of HACCP system in public kitchens, food industry.Education of food workers about Staphyloccocus spp.infections.

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4.3.2. Staphylococcal enterotoxins in foodstuffs

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5. FOODBORNE OUTBREAKS

Foodborne outbreaks are incidences of two or more human cases of the same disease or infection where thecases are linked or are probably linked to the same food source. Situation, in which the observed human casesexceed the expected number of cases and where a same food source is suspected, is also indicative of afoodborne outbreak.

A. Foodborne outbreaks

System in place for identification, epidemological investigations and reporting offoodborne outbreaks

System for identification of foodborne outbreaks is:mandatory and national.It covers: family, general and international outbreaks;and all classes of microbiological agents.An outbreak of foodborne illness may be defined as two or more linked cases of the same illness orthe situation, where the observed number of cases exceeds the expected number.Oubreaks of foodborne infections are notifiable by national Law on Infectious diseases, issued in1995. Public health professionals in regional institutes are requested to report regularly allinvestigated outbreaks of infectious intestinal diseases to the Institute of public health of the RepublicSlovenia, using a preliminary notification form.At the end of investigation a final report is also forwarded by the lead investigator.An outbreak of foodborne illness may be defined as two or more linked cases of the same illness orthe situation, where the observed number of cases exceeds the expected number.

Description of the types of outbreaks covered by the reporting:

Reporting covers:family, general and international outbreaks.It covers all range of microbiological agents.

National evaluation of the reported outbreaks in the country:

Trends in numbers of outbreaks and numbers of human cases involved

In 2006 66 different outbreaks were recorded with 1796 ill persons.From those; 25 were food borne, 31 were transmitted contactly;4 via droplets, aerosol;there were no waterborne outbreaks; 1 nosocomial outbreak and 5 other outbreaks.Agents, which caused the foodborne outbreaks were:Salmonella Enteritidis (16 outbreaks);Calicivirus (3 outbreaks);Staphyloccocus aureus (3 outbreaks);Cryptosporidium parvum (1 outbreak)Gastroenterocolitis, agent not identified (2 outbreaks).

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Relevance of the different causative agents, food categories and the agent/ foodcategory combinations

Agents, which caused the foodborne outbreaks were:Salmonella Enteritidis (16 outbreaks);Calicivirus (3 outbreaks);Staphyloccocus aureus (3 outbreaks);Cryptosporidium parvum (1 outbreak)Gastroenterocolitis, agent not identified (2 outbreaks).Cause of enteral outbreaks:patient/ carrier (4 outbreaks);chicken (2 outbreaks);fish (1 outbreak);home made cream cake (1 outbreak);beefsteak (1 outbreak);other.

Relevance of the different type of places of food production and preparation inoutbreaks

Number of foodborne outbreaks increased for 79% in comparison with 2005, but is still for21% lower than 5­years average. 64% of foodborne outbreaks in 2006 were caused by Salmonella Enteritidis. 99,99%comparability among epidemic, Salmonella Enteritidis from source of outbreaks andSalmonella Enteritidis of ill persons, was confirmed by PFGE in all outbreaks.

Descriptions of single outbreaks of special interest

Salmonella outbreak in summer sport camp for children; the same Salmonella Enteritidis PFGEserotype was found in cakes and in feces of children and kitchen workers (99,99%comparability).Imported Salmonella Enteritidis outbreak from Serbia; from 38 bus pasangers from Slovenia,who went for a trip to Serbia and ate supper in Belgrade, 31 went ill. From 31 patients, 13 werediagnosed with Salmonella sepsis. No one died. Food samples were not available. Serotypes ofSalmonella spp. of patients were the same according to PFGE analysis.

Control measures or other actions taken to improve the situation

Improvement of general hygienic conditions in kitchens, cleaning and disinfection of public kitchens;education of public kitchen workers about food hygiene;excluding of public kitchen workers with diarrhea from food handling;excluding of public kitchen workers from food handling because of lack of knowledge of foodhygiene;control of HACCP system;booklet with information about Salmonella in food for consumers.

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Table Foodborne outbreaks in hum

ans

Causative agent

General

outbreak

Household

outbreak

Total Num

ber of

persons

Food im

plicated

Type of

evidence for

implication

of the food

Place where

food was

consum

ed

Contributing

factors

ill (in total)

died

in hospital

Food (sub)category

Suspected as a source

Confirmed as a source

1 2

3 4

5 6

7 8

9 10

Cryptosporidium ­ C. parvum

18

00

carrier

1Epidem

iological

evidence

arrest

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

16

00

carrier

1Epidem

iological

evidence

home for the

elderly

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

16

00

carrier

1Epidem

iological

evidence

hospital

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

18

02

lunch

1Epidem

iological

evidence

school

breakdow

n of

HACCP

Food borne viruses ­ calicivirus (including norovirus)

110

01

carrier

1Epidem

iological

evidence

school cam

punknow

n

Food borne viruses ­ calicivirus (including norovirus)

113

00

carrier

1Epidem

iological

evidence

home for the

elderly

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

113

07

carrier

1Epidem

iological

evidence

hospital

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

114

00

food ­ unknow

n1

Epidem

iological

evidence

hotel

breakdow

n of

HACCP

Food borne viruses ­ calicivirus (including norovirus)

114

00

unknow

n1

Epidem

iological

evidence

health resort

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

117

00

unknow

n1

Epidem

iological

evidence

canteen

breakdow

n of

HACCP

Food borne viruses ­ calicivirus (including norovirus)

120

01

unknow

n1

Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

122

00

carrier

1Epidem

iological

evidence

restaurant

breakdow

n of

HACCP

Food borne viruses ­ calicivirus (including norovirus)

126

00

unknow

n1

Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

131

00

carrier

1Epidem

iological

evidence

health resort

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

134

01

food ­ unknow

n1

Epidem

iological

evidence

factory of

medicines

breakdow

n of

HACCP

Food borne viruses ­ calicivirus (including norovirus)

140

03

food ­ unknow

n1

Epidem

iological

evidence

hotel

breakdow

n of

HACCP

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Food borne viruses ­ calicivirus (including norovirus)

143

03

carrier

1Epidem

iological

evidence

home for the

elderly

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

144

00

carrier

1Epidem

iological

evidence

home for the

elderly

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

171

00

unknow

n1

Epidem

iological

evidence

health resort adn

home for the

eldely

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

172

01

food ­ unknow

n1

Epidem

iological

evidence

school

breakdow

n of

HACCP

Food borne viruses ­ calicivirus (including norovirus)

174

01

carrier

1Epidem

iological

evidence

home for the

elderly

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

178

00

carrier

1Epidem

iological

evidence

home for the

eldely

unknow

n

Food borne viruses ­ calicivirus (including norovirus)

185

01

food ­ unknow

n1

Epidem

iological

evidence

home for the

elderly

breakdow

n of

HACCP

Food borne viruses ­ rotavirus

110

01

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ rotavirus

111

04

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ rotavirus

113

01

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ rotavirus

117

05

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ rotavirus

167

00

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Food borne viruses ­ rotavirus

184

00

carrier

1Epidem

iological

evidence

home for the

elderly

unknow

n

Salmonella ­ S. Enteritidis

18

08

home made cream cake

1laboratory

confirm

edfamily

celebration

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

15

00

roast fish and potato salad

1Laboratory

confirm

edcanteen

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

15

02

food

1Laboratory

confirm

edrestaurant

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

17

01

carrier

1Laboratory

confirm

edrestaurant

breakdow

n of

HACCP

Salmonella ­ S. Enteritidis

19

02

carrier

1laboratory

confirm

edhome for the

elderly

unknow

n

Salmonella ­ S. Enteritidis

114

00

food

1Laboratory

confirm

edkindergarten

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

114

01

unknow

n1

Epidem

iological

incidence

restaurant

breakdow

n of

HACCP

Salmonella ­ S. Enteritidis

115

02

unknow

n1

Epidem

iological

evidence

school cam

pdeficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

115

07

food

1laboratory

confirm

edrestaurant

deficiencies in

the preparation

or food handling

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Salmonella ­ S. Enteritidis

116

02

roast m

eet

1Laboratory

confirm

edrestaurant

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

119

02

chicken

1laboratory

confirm

edrestaurant

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

120

01

Tartar beefsteak

1Laboratory

confirm

edrestaurant

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

122

00

food­unknown

1Epidem

iological

evidence

school cam

punknow

n

Salmonella ­ S. Enteritidis

131

013

food (smoked ham

, vegetables, roast m

eet, sweets)

1laboratory

confirm

ed

excursion

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

133

05

food ­ unknow

n1

Epidem

iological

evidence

school and

kindergarten

unknow

n

Salmonella ­ S. Enteritidis

173

06

food ­ unknow

n1

Epidem

iological

evidence

restaurant

deficiencies in

the preparation

or food handling

Salmonella ­ S. Enteritidis

198

09

unknow

n1

Epidem

iological

evidence

school

unknow

n

Staphylococcus ­ S. aureus

16

00

carrier

1Laboratory

confirm

edrestaurant

breakdow

n of

HACCP

Staphylococcus ­ S. aureus

18

00

carrier

1Laboratory

confirm

edschool cam

punknow

n

Staphylococcus ­ S. aureus

138

00

food

1Laboratory

confirm

edschool cam

punknow

n

Unknown

15

00

unknow

n1

Epidem

iological

evidence

kindergarten

unknow

n

Unknown

17

00

unknow

n1

Epidem

iological

evidence

school

unknow

n

Unknown

110

00

unknow

n1

Epidem

iological

evidence

school cam

punknow

n

Unknown

116

00

carrier

1Epidem

iological

evidence

school

unknow

n

Unknown

116

00

carrier

1Epidem

iological

evidence

school

unknow

n

Unknown

117

00

food

1Epidem

iological

evidence

rustic cottage

deficiencies in

the preparation

or food handling

Unknown

117

01

carrier

1Epidem

iological

evidence

school

unknow

n

Unknown

119

00

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Unknown

121

00

food ­ unknow

n1

Epidem

iological

evidence

school

unknow

n

Unknown

136

04

unknow

n1

Epidem

iological

evidence

canteen

breakdow

n of

HACCP

Unknown

1134

00

carrier

1Epidem

iological

evidence

school

unknow

n

Yersinia ­ Y

. enterocolitica

133

00

carrier

1Epidem

iological

evidence

kindergarten

unknow

n

Slovenia 2006 Report on trends and sources of zoonoses

Slovenia 2006 310