Exam 3 Objectives Flashcards

(91 cards)

1
Q

Where can you find S. epidermis?

A

In the normal skin microbiota.

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2
Q

Where can you find S. saprophyticus?

A

In the normal vaginal microbiota.

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3
Q

What infections can S. saprophyticus cause?

A

UTIs

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4
Q

What infections can S. aureus cause?

A

MRSA, impetigo, food poisoning, toxic shock syndrome.

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5
Q

What is differential media?

A

Media that changes its appearance due to some characteristic of the organism.

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6
Q

What are some examples of differential media?

A

Fermentation tubes or DNase agar.

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7
Q

What is selective media?

A

Media that encourages some growth while inhibiting others

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8
Q

What is an example of selective media?

A

CNA-BA

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9
Q

Why is CNA-BA considered selective and differential?

A

The antibiotics, colistin and nalidixic acid (CNA) inhibit the growth of Gram-negative organisms making Columbia CNA selective as well as differential.

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10
Q

What does a catalase test do?

A

Tests for the enzyme catalase which breaks down hydrogen peroxide into water and oxygen.

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11
Q

Why is catalase important?

A

Hydrogen peroxide is a toxic form of oxygen and a byproduct of aerobic respiration; bacteria need some way to break it down.

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12
Q

What does a positive test for catalase look like?

A

When hydrogen peroxide is put on the organism, a vigorously bubbling will occur.

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13
Q

Do Staphs or Strepts test positve for coagluase?

A

Staphs

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14
Q

What does a coagulase test do?

A

Tests to see if blood plasma can be turned into a blood clot by coagulase.

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15
Q

Why are blood clots important for bacteria?

A

Clots can help bacteria establish infections and protect themselves.

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16
Q

What media was used for the coagulase test?

A

Rabbit plasma.

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17
Q

What does a positive coagulase test look like?

A

A clot will be formed in the test tube.

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18
Q

What does a Novobiocin Disk test do?

A

Test how sensitive or resistant Staphs are to the antibiotic Novobiocin.

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19
Q

How can we tell is a Staph is resistant or sensitive to Novobiocin?

A

Sensitive: large zone of inhibition.
Resistant: small zone of inhibition.

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20
Q

How do you perform a Novobiovin Disk test?

A

Create a lawn of bacteria.
Put the antibiotic disk in the middle.

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21
Q

What oxygen classifications do more Strepts belong in?

A

Most are facultative anerobes or anerobes.

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22
Q

What is a capnophile?

A

An organism that grows better in a high concentration of CO2.

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23
Q

What do we do to accommodate some Strepts being capnophiles?

A

We grow the Strepts in a candle jar to raise the concentration of CO2.

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24
Q

What are some infections S. pyogenes cause?

A

Strept throat (which can turn into scarlet fever), impetigo, necrotizing fascitis, autoimmune complications, and rheumatic fever (which can lead to heart valve damage).

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25
Where can S. agalactiae be found?
In the normal microbiota vaginally ~30%
26
What infections can S. agalactiae cause?
Neonatal meningitis.
27
What infections can S. agalactiae cause?
Neonatal meningitis.
28
What infections can S. pneumoniae cause?
Pneumonia, ear infections, and meningitis.
29
What infections can S. mitis cause?
Tooth decay and plaque.
30
Where can S. mitis be found?
Normal mouth microbiota.
31
What is specifc about S. mitis and S. pneumoniae?
The both can make a capsule for protection.
32
Where can Enterococcus faecalis be found?
In the normal microbiota of the large intestine.
33
What are Lancefield groups based on?
They are based in the carbohydrate surface antigens of Strept.
34
What does B-hemolysis do?
Lysis all red blood cells.
35
What is O hemolysin?
Inhibited by oxygen.
36
What is S hemolysin?
Stable in oxygen.
37
What does Alpha-hemolysis do?
Partial red blood cell lysis.
38
What does Gamma-hemolysis do?
No red blood cell lysis.
39
How do B-hemolysis bacteria look on blood agar?
The media becomes clear or yellow especially around the stabs in the agar.
40
How do Alpha-hemolysis bacteria look on blood agar?
The media becomes greenish/brown especially around the stabs in the agar.
41
How do Gamma-hemolysis bacteria look on blood agar?
The media does not change color or appearance.
42
How did we innoculate a bile esculin test?
We innoculate the slant just like normal.
43
What are we testing for in a bile esculin test?
Testing to see if the organism can break down the polysaccharide esculin into esculatin and glucose.
44
What group of Strepts test positive for a bile esculin test?
Group D Strepts.
45
What does a positive bile esculin look like?
A black color change will occur.
46
How did we innoculate a hippurate test?
Inoculate the solution like normal.
47
What are we testing for in a hippurate test?
We testing to see if an organism can use hippurate hydrolase to break down hippurate into benzoate and glycine.
48
What group of Strepts test positive for the hippurate test?
Group B Strepts.
49
What reagent do we add to hippurate tests after incubation?
Ninhydrin.
50
What does a positive hippurate test look like?
A purple color change occurs.
51
Why is MacConkey agar both differential and selective?
MacConkey agar contains both bile salts and lactose which acts both selectively and differentially. This bile salt component is selective to gram-negative enteric bacteria, and inhibits the growth of most gram-positive bacteria.
52
What tests make up the MIViC tests?
Indole test, Methyl Red test, Voges-Proskauer test, and Citrate test.
53
What media did we use in the indole test?
We used tryptophan enriched broth.
54
What are we testing for in an indole test?
Tests if tryptophanase can break down tryptophan into indole, pyruvate, and NH3.
55
What is indole?
Indole is an amino acid.
56
What reagent do we add to an indole test after incubation?
Kovac's reagent.
57
What does a positive indole test look like?
A red ring is sitting on top of the media after the reagent is added.
58
What are we testing in a methyl red test?
Tests if the organism uses the mixed acid fermentation path when given glucose.
59
What are mixed acid fermentation pathway products?
Succinic acid, lactic acid, formic acid, acetic acid.
60
What reagent is added after incubation of a methyl red test?
Methyl red, which acts as a pH indicator.
61
What does a positive methyl red test look like?
A red color change occurs.
62
What are we testing for in a Voges-Proskauer test?
If the organism produces acetoin, which breaks down into 2,3 butanediol which has a pH of 6.
63
What reagent is added to a Voges-Proskauer after incubation?
Voges-Proskauer A and B in a 3:1 ratio.
64
What does a positive Voges-Proskauer test look like?
A dark/muddy red color change.
65
What are we testing in a citrate test?
Tests if an organism can break citrate into NH3 using citrase.
66
What pH indicator is in the slant?
Brothymol blue.
67
What does a positive citrate test look like?
A blue color change (blue signifies that the media has turned alkaline).
68
What's special thing do we have to do to the cap of citrate and urea tests?
Leave it loose to let in oxygen.
69
What are we testing for in a urea test?
Tests if organism can use urease to break down urea into 2 NH3 + CO2.
70
What is formed if 2 NH3 + CO2 is combined with water?
Ammonium carbonate (NH4)2CO3 which is basic.
71
What pH indicator is in the slant?
Phenol red.
72
What does a positive urea test look like?
A pink alkaline color change.
73
What does the Kliger's Iron Agar (KIA) test for?
Sugar utilization and hydrogen sulfide production.
74
What does the KIA agar contain to test for sugar utilization?
0.1% glucose, 1% lactose, and the pH indicator phenol red.
75
How are the acidic and basic colors shown in the slant?
Acidic=Yellow Basic=Red
76
What components of the KIA agar test for hydrogen sulfide?
Sodium thiosulfate (a source of sulfur) and ferric ammonium citrate (tests for hydrogen sulfide production).
77
How does ferric ammonium citrate show hydrogen sulfide production?
The hydrogen sulfide reacts with the iron to make iron sulfide which shows as a black ppt.
78
How do we innoculate the KIA slant?
We stab into the shallower butt portion and then streak to get the heaviest inoculum in the butt of the tube (the place with the least oxygen).
79
What does an A/A test result mean?
It means both the slant and the butt were yellow and the organism ferments glucose and lactose.
80
What does a K/K test result mean?
It means both the slant and the butt were red and the organism cannot ferment glucose or lactose.
81
What does a K/A test result mean?
It means the slant was red and the butt was yellow and the organism can ferment glucose but not lactose.
82
What does a black color anywhere in the slant mean?
It means the organism produces hydrogen sulfide.
83
What do creaks or bubbles in the agar mean?
Gas was produced during fermentation.
84
What 3 things do we test in the SIM test?
Hydrogen sulfide production, indole production, and motility.
84
What 3 things do we test in the SIM test?
Hydrogen sulfide production, indole production, and motility.
85
How does a positive SIM test look for hydrogen sulfide production?
A black color change.
86
How does a positive SIM test look for indole production?
A red ring is present when Kovac's reagent is added.
87
How does a positive SIM test look for motility?
The whole tube is cloudy, not just around the stab.
88
How do we innoculate a SIM test?
Stab straight down and up in the media.
89
How do we create a wet mount?
Use a glass pipet to drop a couple of drops onto a glass slide. Put a plastic coverslip over the drops, creating air bubbles.
90
How do we read a wet mount under the microscope?
Find the edge of an air bubble in 4x and focus. Move up to 40x, focus, and look outside the edge of the bubble.