T3: Mycobacterium (PART 2) Flashcards

1
Q

Special requirements for isolation of M. haemophilum

A

30-32 C and requires hemin

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2
Q

Advantages of the amplified direct DNA probe for ID of M. tuberculosis in a sputum specimen

A

*

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3
Q

Disadvantages of the amplified direct DNA probe for ID of M. tuberculosis in a sputum specimen

A

*

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4
Q

Runyon Groups:

Group I

A

Photochromogens

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5
Q

Runyon Groups:

Group II

A

Scotochromogens

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6
Q

Runyon Groups:

Group III

A

Nonchromogens

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7
Q

Runyon Groups:

Group IV

A

Rapid Growers

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8
Q

Sputum Processing for M. tuberculosis

- decontamination methods

A
    • Eliminate normal flora from the non-sterile samples
  • homogenization to release the bacteria from the sample and allow access to the nutrient present in the media
  • Homogenization: N-acetyl-cystine
  • Decontaminant: NaOH
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9
Q

Sputum Processing for M. tuberculosis

- concentration of NaOH

A
  • 2% NaOH is optimal to decontaminate but not kill all the mycobacteria
    Centrifugation: 3000-38000 x g or higher
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10
Q

Sputum Processing for M. tuberculosis

- smear staining

A

AFB stain on smear

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11
Q

Common members in Group I/Photochromogens

A
M. kansasii
M. marinum 
M. simiae 
M. genavense 
M. asiaticum
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12
Q

Common members in Group II/Scotochromogens

A
M. scrofulaceum  
M. szulgai 
M. xenopi 
M. celatum 
M. gordonae 
M. flavescens
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13
Q

Common members in Group III/Nonchromogens

A

M. avium
M. paratuberculosis
M. terrae
M. haemophilum

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14
Q

Common members in Group IV/Rapid Growers

A

M. fortuitum
M. chelonae
M. abcessus

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15
Q

Three members of the M. tuberculosis complex

A

M. tubeculosis
M. africanum
M. bovis

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16
Q

What is the setup of a skin culture for mycobacteria? (include temp, media etc)

A

EVERYTHING must be set up at 37C with bottle and solid media. Then if it is skin or soft tissue, also set up at 30-32C

17
Q

Appearance on an agar plate:

- M. tuberculosis

A

rough and buff

18
Q

Appearance on an agar plate:

- M. kansasii

A

buff colored when in the dark and yellow colored when exposed to light

19
Q

Appearance on an agar plate:

- M. xenopi

A

pale yellow to yellow orange regardless of light (very slower grower, loves 42C)

20
Q

Appearance on an agar plate:

- M fortuitum

A

rapid, rhizoids and rust appearance

21
Q

M. bovis:

- how does it affect the TB skin test

22
Q

M. bovis

- how it is used in cancer patients

A

BCG treatment in patients with bladder cancer

23
Q

M. bovis:

- how it is identified

A
  • water doplet-like colonies
  • Positive with the TB complex DNA probe
  • Susceptibility to T2H
24
Q

M. bovis

- relationship to BCG

A

An “attenuated” strain of M. bovis that does not cause disease but can stimulate the immune response is used for the Bacillus Calmette-Guerin (BCG) vaccine

25
Which mycobacteria are inhibited by T2H?
M. bovis
26
Which mycobacteria are Nitrate positive?
``` M. tuberculosis M. kansasii M szulgai M flavescens M fortuitum ```
27
How can urease be used as a clue to differentiate scotochromogens into pathogens vs. nonpathogenic
Urease positive means its probably a pathogen, negative urease usually indicates a contaminant
28
Methods for identifying M. leprae
*
29
Tests that differentiate M. tuberculosis and M. bovis
Niacin, Nitrate, and T2H M. tuberculosis: Niacin (+), Nitrate (+) T2H (resistant) M bovis: Niacin (-), Nitrate (-) T2H (susceptible)
30
Key biochemical reactions for differentiating members of the rapid growers group
MAC and Iron uptake
31
Key biochemical reactions for differentiating members of the scotochromogens group
Urease and Tween
32
Key biochemical reactions for differentiating members of the photochromogens group
photochromogenicity and temperature