MYCOBACTERIA Flashcards

1
Q

i. Mycobacterium tuberculosis
ii. Mycobacterium bovis
iii. Mycobacterium africanum
iv. Mycobacterium canetti
v. Mycobacterium microti

A

. Mycobacterium tuberculosis complex

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2
Q

Non-tuberculous mycobacteria

A

Group I – photochromogens, produces
pigment when there is light, no light = no
pigment (photo – light, chromo –
pigment)
ii. Group II – scotochromogens, produces
pigment with and without the presence
of light.
iii. Group III – non-photochromogens, does
not produce any kind of pigment.
➢ Group I, II, III are slow
growers.
iv. Group IV – rapid growers

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3
Q
  • Slender, slightly curved or straight, rod-shaped organisms
A

MYCOBACTERIA

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4
Q
  • Non-motile and do not form spores
A

MYCOBACTERIA

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5
Q
  • The cell wall has extremely high lipid content; thus, mycobacterial cells
A

MYCOBACTERIA

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6
Q
  • Resist staining with commonly used basic aniline dyes, such as those used in the Gram stain, at room temperature.
A

MYCOBACTERIA

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7
Q
  • Take up dye with increased staining time or application of heat but resist decolorization with acid-ethanol
A

MYCOBACTERIA

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8
Q
  • This characteristic is referred to as acid fastness—hence, the term AFB—and
A

MYCOBACTERIA

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9
Q

strictly aerobic, but increased carbon dioxide (CO2) will enhance the growth of some species.

A

MYCOBACTERIA

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10
Q
  • Cause pulmonary tuberculosis
A

MYCOBACTERIA

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11
Q
  • Studied using AFS (Acid Fast Staining)
A

MYCOBACTERIA

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12
Q
  • Important component is the Mycolic acid (targeted by the antibiotics that are used
A

MYCOBACTERIA

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13
Q
  • Antibiotics of Mycobacteria
A

Isoniazid, Rifampin

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14
Q
  • Consists of M. tuberculosis, M. bovis
A

MYCOBACTERIUM TUBERCULOSIS COMPLEX

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15
Q
  • (including the vaccination strain bacillus Calmette-Guérin), M. africanum, M. canettii, and
    M. microti. M. africanum
A

MYCOBACTERIUM TUBERCULOSIS COMPLEX

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16
Q

usually a disease of the respiratory tract.

A
  • TB
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17
Q

are acquired from persons with active disease who are excreting viable bacilli by sneezing or talking.

A
  • Tubercle bacilli
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18
Q

an organization of lymphocytes, macrophages, fibroblasts, and
* capillaries.

A

granuloma

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19
Q

or granuloma may be formed

A
  • Hard tubercle
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20
Q

o Granuloma treatment is from

A

9-12 months

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21
Q

screening test or the positive PPD (purified protein derivatives) skin test also known as Mantoux skin test.

A
  • Clinical diagnosis of primary TB
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22
Q

ositive PPD (purified protein derivatives) skin test also known as

A

Mantoux skin test.

23
Q
  • Other tests for pulmonary tuberculosis
A

X-ray, culture of the sputum, AFS using the sputum

24
Q

Diagnosis is confirmed by

A

y stained smear and culture of sputum, gastric aspirates, or bronchoscopy specimens

25
o Aside from your lungs, it can also infect other organs through hematogenous spread (spread through blood circulation)
* Extrapulmonary Tuberculosis
26
refers to the seeding of many organs outside the pulmonary tree with AFB through hematogenous spread. (sesame seeds)
* Miliary TB
27
unexplained pleural effusion with mononuclear pleurocytosis, manifests as cough, fever, and chest pain, resembling the presentation of bacterial pneumonia.
* Pleurisy
28
– inflammation of the lymph nodes
* Lymphadenitis
29
of the spine is referred to as Pott disease.
* Skeletal TB
30
, skinny, and not able to stand up
o Positive in TB
31
examination usually reveals an elevated protein level, decreased glucose level, and a predominance of lymphocytes.
* Cerebrospinal fluid (CSF)
32
malachite green, egg white)
LJ medium
33
characterized as cauliflower appearance.
* Mycobacterium tuberculosis
34
colonies typically raised, with a dry, rough appearance
* Mycobacterium tuberculosis
35
nonpigmented and classically described as being buff-colored
* Mycobacterium tuberculosis
36
* Optimal growth occurs at
35° C to 37° C.
37
* For pulmonary TB, treatment typically involves
9-month course of therapy with isoniazid and rifampin, usually once per day the first month and twice a week thereafte
38
o for severe/chronic TB, therap
12 months
39
first life of drugs for Pulmonary Tuberculosis.
o isoniazid and rifampin
40
inhibits mycolic acid
o Isoniazid
41
inhibits RNA polymerase
Rifampin
42
* Regimens also include a 2- to 8-week initial course of
streptomycin or ethambutol
43
may be added to the regimen if there is a suspicion of lowered cellular immunity and a need to obtain bactericidal levels of antimycobacterial activity intracellularly in macrophages.
* Pyrazinamide (PZA)
44
defined as resistance to at least isoniazid and rifampin
* MDR-TB (multi drug resistant TB)
45
is defined as resistance to isoniazid and rifampin plus resistance to any fluoroquinolone and at least one of three injectable second-line anti-TB drugs—the aminoglycosides amikacin, kanamycin, or capreomycin.
* Extensively drug-resistant TB (XDR-TB)
46
RIPES (Rifampin, Isoniazid, Pyrazinamide, Ethambutol, Streptomycin)
o Primary drugs
47
Aminoglycosides Amikacin, Kanamycin, or Capreomycin.
o Secondary drugs
48
* TB primarily in cattle but also in other ruminants, as well as in dogs, cats, swine, parrots, and humans. (domestic animals)
MYCOBACTERIUM BOVIS
49
* The disease in humans closely resembles that caused by M. tuberculosis and is treated similarly.
MYCOBACTERIUM BOVIS
50
* days of incubation at C.
21 , 37°C
51
o niacin-negative o do not reduce nitrate o do not grow in the presence of (T2H) thiophene-2-carboxylic acid hydrazide
* Test results of M. bovis
52
* Causes TB in Tropical Africa
MYCOBACTERIUM AFRICANUM
53
* Associated with AIDS patients
MYCOBACTERIUM CANETTI
54
* Causes TB for both immunocompromised and competent
MYCOBACTERIUM MICROTI