MI: Mycobacterial Diseases Flashcards

1
Q

How can mycobacteria be categorised?

A

Rapid-growing and slow-growing

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2
Q

List three types of mycobacterial complex.

A

Mycobacterium tuberculosis complex

  • Mycobacterium tuberculosis
  • Mycobacterium bovis

Mycobacterium avium complex

  • Mycobacterium avium
  • Mycobacterium intracellulare

Mycobacterium abscessus complex

  • Mycobacterium abscessus
  • Mycobacterium massiliense
  • Mycobacterium bolletii
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3
Q

Describe the morphology of mycobacteria.

A
  • Non-motile rod-shaped bacteria
  • Relatively slow-growing
  • Cell wall composed of mycolic acids, complex waxes and glycoproteins
  • Acid-alcohol fast
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4
Q

What is used as a screening test for mycobacterial infections?

A

Auramine stain

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5
Q

How are non-tuberculous mycobacterial infections transmitted?

A
  • NOT person-to-person
  • From the environment
  • May be colonising rather than infecting
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6
Q

List three examples of slow-growing non-tuberculous mycobacteria and the diseases that they cause.

A

Mycobacterium avium intracellulare

  • May invade bronchial tree or pre-existing bronchiectasis/cavaties
  • Disseminated infection in immunocompromised patients

Mycobacterium marinum

  • Swimming pool granuloma

Mycobacterium ulcerans

  • Skin lesions (e.g. Bairnsdale ulcer, Buruli ulcer)
  • Chronic progressive painless ulcer
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7
Q

List three examples of rapid-growing non-tuberculous mycobacteria.

A
  • Mycobacterium abscessus
  • Mycobacterium chelonae
  • Mycobacterium fortuitum
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8
Q

List some risk factors for NTM.

A

Age

Underlying lung disease

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9
Q

How is Mycobacterium avium intracellulare treated?

A
  • Clarthromycin/azithromycin
  • Rifampicin
  • Ethambutol
  • +/- streptomycin/amikacin
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10
Q

What are the two types of Mycobacterium leprae infection?

A
  • Paucibacillary tuberculoid - few skin lesions (usually <5), robust T cell response, low number of bacteria in the body
  • Multibacillary lepromatous - multiple skin lesions (usually >5), poor T cell response, high number of bacteria
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11
Q

What is the most common cause of death by infectious agent in the world?

A
  • 1 = HIV
  • 2 = TB (10% of world infected)
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12
Q

How many species are part of the Mycobacterium tuberculosis complex?

A

7 (including Mycobacterium tuberculosis, bovix and africanum)

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13
Q

What is the generation time of Mycobacterium tuberculosis?

A

15-20 hours

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14
Q

What is the infectious dose of Mycobacterium tuberculosis?

A

1-10 bacilli

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15
Q

What are the 2 types of primary TB infection

A
  • Latent TB
    • Asymptomatic
    • Not contagious
  • Active primary TB
    • Symptomatic
    • Infectious
    • Can cause progessive disseminated disease
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16
Q

What is post-primary (secondary) TB?

A

Reactivation or exogenous re-infection

10% chance after primary infection

17
Q

List some risk factors for reactivation of TB.

A
  • Immunosuppression
  • Chronic alcohol excess
  • Malnutrition
  • Ageing
18
Q

List some types of extra-pulmonary TB.

A
  • Lymphadenitis (scrofula) - cervical lymph nodes most commonly
  • Gastrointestinal - due to swallowing of tubercle
  • Peritoneal - ascitic or adhesive
  • Genitourinary
  • Bone and joint - due to haematogenous spread (e.g. Pott’s disease)
  • Miliary TB
  • Tuberculous meningitis
19
Q

Why is it important to take 3 sputum samples when investigating suspected TB?

A

Increases the sensitivity of the smear microscopy

20
Q

What is the turnaround time for smear microscopy and PCR?

21
Q

What is the issue with culturing TB?

A

It takes up to 6 weeks

22
Q

What is the histological hallmark of TB?

A

Caseating granulomas

23
Q

What is NAAT and why is it useful?

A
  • Nucleic acid amplification test
  • Allows speciation and the detection of drug resistance mutations
  • Rapid
24
Q

What are the screening tests for latent TB

A

Tuberculin skin test

Interferon gamma release assay

25
What is the tuberculin skin test (Mantoux test) and how does it work?
A sample of tuberculin is injected intradermally and left for 48-72 hours to observe the response Type IV hypersensitivity (T cell) response to antigen
26
What are the disadvantages of the tuberculin skin test?
* Cross-reacts with BCG * Cannot distinguish between active and latent TB * False negative in immunosuppressed individuals
27
What is an IGRA assay?
* Uses M. tuberculosis specific antigens to stimulate T cell IFN-gamma production which is then measured using ELISA
28
What are the advantags and disadvantges of IGRA assay?
No cross reactivity with other strains Does not distinguish between latent or active TB
29
What do you do if screening tests are positive?
CXR (looks for active TB) if CXR normal - treat with latent TB protocol
30
What is the treatment of latent TB
* 3 months of isoniazid plus rifampicin * Or 6 months of isoniazid
31
What is the treatment of active TB
* **Initiation phase:** rifampicin, isoniazid, pyrazinamide, ethambutol for 2 months * **Continuation phase:** rifampicin plus isoniazid for 4 months
32
List some side-effects of: 1. Rifampicin 2. Isoniazid 3. Pyrazinamide 4. Ethambutol
1. **Rifampicin** * Raised transaminases * CYP450 induction * Orange secretions 2. **Isoniazid** * Peripheral neuropathy * Hepatotoxicity 3. **Pyrazinamide** * Hepatotoxicity 4. **Ethambutol** * Visual disturbance
33
What drug is given to prevent peripheral neuropathy from isoniazid?
Pyridoxine
34
What is DOT?
Direct observation therapy
35
What is multi-drug resistant TB?
Resistant to rifampicin and isoniazid
36
What is extremely drug resistant TB?
Resistant to rifampicin, isoniazid, fluoroquinolones and at least 1 injectable
37
What are the diagnostic challenges of HIV and TB coinfection?
* Clinical presentation is less likely to be classical * Symptoms may be absent if CD4+ count is low * More likely to have extra-pulmonary manifestations * Tuberculin skin test more likely to give false-negative * Low sensitivity for IGRAs
38
What are the treatment challenges of HIV and TB coinfection?
* Timing of treatment * Drug interactions * Overlapping toxicities * Duration of treatment