Fastidious Gram Negative Rods Respiratory Culture Unit Division of Medical Technology Carol Larson...

Preview:

Citation preview

Fastidious Gram Negative RodsRespiratory Culture Unit

Division of Medical Technology

Carol Larson MSEd, MT(ASCP)

Please click audio iconto hear Carol’s narration

• Fastidious– Complex / extensive nutrient requirements

• Faint staining Gram Negative Rods– Safranin counterstain for >2 minutes– Substitute carbolfuschin for safranin

• Serological testing useful

Click icon for audio

General Information

• Causes Pertussis / Whooping cough

• Spread by airborne droplets

• Virulence factors– Attachment to ciliated epithelium of the

upper respiratory tract– Exotoxin – tracheal cytotoxin– Exotoxin - Pertussis toxin– Cell wall endotoxin

Click icon for audio

Bordetella pertussis

Clinical Significance

• Nasopharyngeal swab or aspirate

• Plate at bedside– Regan-Lowe media– Bordet-Gengou media– Methicillin or cephalexin added to media

to inhibit normal flora

• Make smear for DFA screening

Click icon for audio

Bordetella pertussis

Specimen Collection

• 35ºC, 5-10% CO2 for at least 7 days

• Colony morphology– No growth on

BAP & MAC– Bordet-Gengou– Regan-Lowe

Click icon for audio

Bordetella pertussis

Growth Characteristics

• Gram stain– Small, faintly staining gram-negative

coccobacilli

• Oxidase +

• Nitrate –

• Urea –

• Nonmotile

Click icon for audio

Bordetella pertussis

Identification

• Direct fluorescent antibody test

• Agglutination methods

• DNA probes for direct detection in:– Specimen– Culture confirmation

Click icon for audio

Bordetella pertussis

Serological Testing

• Erythromycin is drug of choice

• Vaccination

Click icon for audio

Bordetella pertussis

Treatment & Prevention

What media is used to culture Bordetella pertussis?

Regan-Lowe media and Bordet-Gengou media. Bordetella pertussis will not grow on BAP or MAC. Methicillin or cephalexin can be added to the media to inhibit normal flora.

Francisella tularensis

Clinical Significance• Causes Tularemia – an acute febrile,

HIGHLY INFECTIOUS disease

• Acquire by:– Direct contact with infected animals

(rabbits)– Bite from an insect– Inhalation of infectious aerosols

Click icon for audio

Francisella tularensis

Specimen Collection• Inflammatory material from infected site

• Wear gloves and use biosafety hood

• Do not aerosolize or allow contact with skin or mucous membranes

• CDC: Biosafety Level 2 pathogen

Click icon for audio

Francisella tularensis

Specimen Processing• Requires cysteine / cystine for growth

• Glucose-cystine blood (Francis’) agar

• Grows on– Chocolate– BCYE– Modified TM

Click icon for audio

Francisella tularensis

Growth Characteristics• Strict aerobic

• 35°C with 5-10% CO2 for 7 days

• Colony morphology– BAP & MAC = No growth– CHOC = Small, gray

alpha-hemolytic colonyat 2-5 days

Click icon for audio

Francisella tularensis

Identification• Pale staining gram negative coccobacilli

• Oxidase –

• Catalase – to weak +

• Glucose fermenter

• Nonmotile

Click icon for audio

Francisella tularensis

Serological Testing• Most cases diagnosed serologically

• DFA tests may be performed on specimen

• ELISA and agglutination tests

• Four-fold rise in titer is diagnostic

• Single titer of >=1:160 is presumptive

Click icon for audio

• Streptomycin is drug of choice

Click icon for audio

Francisella tularensis

Treatment & Prevention

What substance is required in culture media in order to grow Francisella?

Cysteine / Cystine

What is the best method for determining if a patient has Tularemia and Why?

Serological testing is best. To actually culture the organism in the laboratory has a high risk for laboratory personnel becoming infected.

• Legionnaires’ disease

• Pontiac Fever

• Transmission: inhalation of the organism in aerosols

• Legionella pneumophila serogroup 1

Click icon for audio

Legionella species

Clinical Significance

• BAL, BW, lung biopsy, pleural fluid

• Avoid aerosolization

• Transport ambient temperature

• Requires cysteine and iron salts for growth

• Buffered Charcoal Yeast Extract agar– Selective media: BCYE + antibiotics

Click icon for audio

Legionella species

Specimen Collection

• Aerobic

• 35°C in 5-10% CO2 for 10 days

• Colony morphology– BAP & MAC = no growth– CHOC = grows slowly– BCYE = convex, grayish

white, glistening with an entire edge at 2-4 days

Click icon for audio

Legionella species

Growth Characteristics

• Thin, faintly staining short to filamentous GNR

• Oxidase wk +

• Catalase wk +

• Non-”F”

• Non-”O”

• Motile:polar flagella

Click icon for audio

Legionella species

Identification

• Specimen screen & Isolate ID– DFA stain and DNA probe

• IFA test of choice (serum)– Four-fold rise in titer to at least 1:128

Click icon for audio

Legionella species

Serological Testing

• Susceptibility testing not routinely performed

• Drug of choice: Erythromycin alone or with Rifampin

Click icon for audio

Legionella species

Treatment and Prevention

What substance is required in culture media in order to grow Legionella?

Cysteine and iron salts.

What populations are most prone to Legionella infections?

Men, cigarette smokers, people with underlying disease, immunocompromised/immunosuppressed patients, people who drink alcohol and nosocomial infections.

• Looked at several organisms

• Clinical significance

• Specimen collection, transport & processing

• Growth characteristics & identification

• Serological testing

• Treatment and prevention

Click icon for audio

Fastidious GNR

Summary

Who am I?

Reagin-Lowe media Gram Stain

Bordetella pertussis

Causes Whooping Cough

Who am I?

BCYE agar Gram Stain

Legionella species

Causes Pontiac Fever

Recommended