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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
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
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006
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
Slovenia 2006 Report on trends and sources of zoonoses
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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.
Slovenia 2006 Report on trends and sources of zoonoses
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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
Slovenia 2006 Report on trends and sources of zoonoses
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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
Slovenia 2006 Report on trends and sources of zoonoses
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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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 84
Amoxicillin
30
11
1
Amoxicillin / Clavulanic acid
30
11
1
Ampicillin
30
12
Trimethoprim + su
lfonamides
Trimethoprim + Sulfamethoxazol
30
11
1
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 85
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 86
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 87
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 88
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 89
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 90
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 91
Amoxicillin
00
Amoxicillin / Clavulanic acid
00
Ampicillin
00
Trimethoprim + su
lfonamides
Trimethoprim + Sulfamethoxazol
00
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 92
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 93
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 94
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 95
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
Slovenia 2006 96
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
Slovenia 2006 97
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 98
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
Slovenia 2006 99
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
Slovenia 2006 100
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 101
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
Slovenia 2006 102
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
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
Slovenia 2006 104
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
Slovenia 2006 105
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
Slovenia 2006 106
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
Slovenia 2006 107
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 108
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
Slovenia 2006 109
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
Slovenia 2006 110
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
Slovenia 2006 111
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 112
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
Slovenia 2006 113
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
Slovenia 2006 114
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 115
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
Slovenia 2006 116
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 117
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
Slovenia 2006 118
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 119
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 120
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
Slovenia 2006 121
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 122
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 123
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 124
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
Slovenia 2006 125
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
Slovenia 2006 126
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
Slovenia 2006 127
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 128
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 129
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
Slovenia 2006 130
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
Slovenia 2006 131
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
Slovenia 2006 132
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 133
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 134
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
Slovenia 2006 135
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
Slovenia 2006 136
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
Slovenia 2006 137
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
Slovenia 2006 138
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 139
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 140
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
Slovenia 2006 141
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
Slovenia 2006 142
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
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 144
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
Slovenia 2006 145
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 146
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
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
Slovenia 2006 148
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
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 150
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 151
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 152
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
Slovenia 2006 153
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 154
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
Slovenia 2006 155
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
Slovenia 2006 156
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 157
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 158
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).
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 229
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).
Slovenia 2006 Report on trends and sources of zoonoses
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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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Slovenia 2006 235
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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Slovenia 2006 245
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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Slovenia 2006 250
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 284
Ampicillin
83
31
11
11
Trimethoprim + su
lfonamides
82
21
11
11
1
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 285
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 286
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 287
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 288
"All animals" stands for E. coli O:157 from monitoring of animals and food in veterinary laboratories.
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 289
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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Slovenia 2006 290
Ampicillin
40
12
1
Trimethoprim + su
lfonamides
40
13
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 291
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 292
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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Slovenia 2006 293
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 294
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 295
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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Slovenia 2006 296
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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Slovenia 2006 298
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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Slovenia 2006 300
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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Slovenia 2006 301
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.
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 302
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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Slovenia 2006 303
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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Slovenia 2006 304
4.3.2. Staphylococcal enterotoxins in foodstuffs
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 305
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.
Slovenia 2006 Report on trends and sources of zoonoses
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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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 308
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
Slovenia 2006 Report on trends and sources of zoonoses
Slovenia 2006 309
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