Midt 2 PP- Jane Flashcards
How do we perform Neisser staining?
1. Neisser -I 2xVol Neisser-II 1xVol Mix these for for about 10 min 2. wash with water 3. Crisoiddine 1-2 min 4. Remove excess stain and dry with filter paper 5. Observer under microscope (immersion)
Clauberg medium
Composed of Glicerin, blood, cystin and tellurite
The specimen reduce the tellurite to different extent –> grey- black colonies.
Gives a garlic smell
Typically used Corynebacterium diphtheria
Löffler medium
Ivory color.
Composed of bovine serum, egg, heart extract.
Rapid growth, strong volutin granule formation.
Oxidase test
Purpose: Detection of cytochrome.oxidase enzyme.
Diagnostic use: Differentiation of obligate aerobes.
Performance:
- Filter paper on microscope slide
- add oxidase reagent ( = parephenylene-diamine derivative)
- add bacteria
- postitive: pink/purple color
oxidase + bacterias: pseudomonas, Neisseria, Vibrio, campylobacter.
Elek’s test
A filter paper strip is buried in the agar before it hardens, this paper have antitoxin on it. If the toxin binds the antitoxin we get a precipitation arch.
This test is used to test the toxigenicity for diphtheria.
Coagulase test
- Tube coagulase test: inoculating the bacteria into citrate treated rabbit plasma, coagulation occurs in a few hours.
- Clumping test: fibrinogen-coated particles endocoagulase binds fibrinogen. Mix the bacteria with fibrinogen-bound latex particles on microscope slide –> clumping bacteria ( in a few sec)
Coagulase +: St. aureus
Coagulase -: all other staphylococci
Catalase test
Aim: to diff between staph and street
Performance: mix the bacteria with H2O2 –> strong bubbling response if positive.
H2O2 –> H20 + O2