Micro Lab Flashcards

0
Q

CNS

A

Coagulase negative staphylococci
S. Epidermidis
A. Saprophyticus

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1
Q

What are the virulence factors if s. Aureus?

A
Coagulase
DNase- digest DNA
Hemolysin αtoxin-β hemolysis
Pigment staphyloxanthin
Ferments mannitol to produce acid
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2
Q

Beta hemolysis

A

Clear zone in blood agar

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3
Q

Alpha hemolysis

A

Greenish discoloration

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4
Q

Gamma hemolysis

A

No effect on blood cells

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5
Q

Group A streptococci

A

Streptococcus pyogenes

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6
Q

Group B strep

A

A. Agalactiae

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7
Q

Group C

A

Zoonoses

A. Dusgalactiae

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8
Q

Fermentation tests

A

Durham tube sugar fermentation a
Mixed acid fermentation (methyl red test)
2,3 butanediol fermentation (Vogues-Proskauer test)
Citrate test

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9
Q

Durham tubes

A

Ferment sugar? Acid produced. Maybe gas too. Acid? Red–>yellow. Gas? Displacement of medium from the Durham tube.

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10
Q

Mixed-acid fermentation

A

Methyl red–> turns red if acid is present some gram negative intestinal bacteria produce a number if organic acids (formic, succinic, lactic, acetic)
Positive result is red. Negative is yellow.

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11
Q

2,3 butanediol fermentation

A

Voges-Proskauer test
Does a neutral end product 2,3 butanediol exist? Important test for determining within enterobacteriaceae. What is negative for MR will usually be positive for VP provided they are enterobacteriaceae
Positive result is red. Negative is yellow or copper

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12
Q

Citrate test

A

Organisms that metabolize citrate release ammonia, making the medium a deeper Prussian blue (basic). Green(-)–> blue(+)

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13
Q

Why is it important to do the o/f glucose test before any other of the fermentation tests? Fermentation tests–>MR, VP, Durham tubes, citrate
Oxidase tests–> oxidase, catalase, nitrate

A

If your organism is only oxidative and not capable if fermenting sugars, don’t do the fermentation tests. Waste of time.

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14
Q

Amylase

A

Degrade starch

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15
Q

Cellulose

A

Degrade cellulose

16
Q

Protease

A

Degrade protein, casein and gelatin and polypeptides into amino acids

17
Q

Lipase a

A

Degrade triglycerides into fatty acids and glycerol

18
Q

Tryptophanase

A

Pyruvate and indole

19
Q

Starch hydrolysis

A

Bacteria that hydrolyze starch have amylases that degrease the starch molecule into molecules of maltose, glucose, and dextrins.
Clear zone–amylase present, hydrolyzing starch.

20
Q

Casein hydrolysis

A

Milk agar

Clear zone means proteolysis of casein.

21
Q

Fat hydrolysis

A

Lipases degrade triglycerides into fatty acids and glycerol. Spirit blue agar contains tributyrin, a simple animal triglyceride that serves as a substrate for lipases. Dark blue precipitate, zone of clearing positive

22
Q

Tryptophan degradation

A

Bacteria that have the ability to degrade the amino acid tryptophan produce indole, ammonia, and pyruvic acid. (Pyruvic acid is useful to the organism) Kovacs reagent is used to see if degradation of tryptophan has occurred. Kovacs turns red if indole is present.

23
Q

Urea hydrolysis

A

Urease–> splits molecule into carbon dioxide and ammonia. Used to seperate out the enteric bacteria proteus, providencia, and morganella. Positive is a beautiful pink color. Negative is yellow.

24
Q

What is the best wavelength for killing bacteria?

A

260 nm

Pyramidine dimer

25
Q

Multiple test technique (sim, etc)

Look over nitrate test

26
Q

Virulent E. coli

27
Q

Coliforms

A

Ferment lactose

28
Q

SIM

A

Contains casein, ferrous salts, agar
Tryptophan–>indole–>Kovacs–>red
Cysteine–>hydrogen sulfide–>ferrous–>black
Motility–>agar

29
Q

Killers iron agar

A

Alkaline (red)
Acid (yellow)
Black(h2s)

30
Q

IMViC

A

Indole
Methyl red
Voges
Citrate

31
Q

Red slant/yellow butt

A

Glucose was utilized only.
Oxidative on top.
Fermentation in bottom.

32
Q

Yellow slant/yellow butt

A

Glucose and lactose utilized.
Acids produced–> yellow
Because of fermentation.