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2. Overview: Mycobacteria: Classification
Pathogenesis of M.tuberculosis
MTB disease
Diagnosis of MTB
Treatment of MTB
Summary of Key Features
3. Mycobacteria: Classification All are Acid fast bacilli (Kinyoun or Ziehl-Neelsen stain)- heat or phenol plus carbol fuschin- destain with acid-alcohol
DO NOT stain by Gram stain- lipids, waxes are impermeable to stain unless heated or treated with phenol
“Cording”: rope like formation of bacilli: - most common for M.tuberculosis
4. Mycobacteria: Classification Nontuberculous Mycobacteria (NTM)- M. avium-intracellulae complex- M. kansasii- M. chelonae (rapid grower)
Mycobacterium tuberculosis complex- M. tuberculosis- M. bovis- M. africanum- M. microti, - M. canettii, - M. pinnipedii
5. Mycobacterium tuberculosis Aerobe
Acid fast bacilli
Mycolic acid, waxes & lipids in cell wall
Slow growing (3 – 8 weeks to grow on agar)
Risk Group 3
Forms “Infectious Droplet Nuclei”: remain airborne for long time
6. Pathogenesis: M.tuberculosis Humans are the only reservoir
Inhalation of droplet nuclei containing M.tuberculosis
Replication in lungs (granuloma formation)
Lymphohematogenous spread: dissemination throughout body inside macrophages
Cell-mediate immune response leads to granuloma formation:
Latent infection
Reactivation
7. Pathogenesis: M.tuberculosis Humans are the only reservoir
Inhalation of droplet nuclei containing M.tuberculosis
Replication in lungs (granuloma formation)
Lymphohematogenous spread: dissemination throughout body inside macrophages
Cell-mediate immune response leads to granuloma formation:
Latent infection
Reactivation
8. Granuloma formation: Host Defense by “walling off” Granuloma formation:activated lymphocytes, macrophages, Langhans giant cells, fibroblasts and capillaries
Caseous necrosis: ? leads to liquefaction of necrotic tissue leads to cavitation in lungs
MTB in granuloma ? latent for years and then if immunity wanes the AFB can reactivate
9. Granuloma: M.tuberculosis
10. Key Virulence Factors of Mycobacteria tuberculosis Infectious droplet nuclei
Resistant cell wall:- waxes, lipids, mycolic acid
Intracellular survival
Latency
11. Survival within Macrophages
12. Student Presentation: Role of Intracellular survival in Pathogenesis of M.tuberculosis
13. Types of Infections: Acute infection: pneumonia [pulmonary TB]
Latent chronic infection ? granuloma in lungs or any other site in the body
Can manifest from any body organ or site so can present in many different ways
14. Mycobacterium tuberculosisPneumonia: Chest X-ray Infiltrates
Nodules
Calcified nodules
15. Infection Control Issues: Respiratory TB 35% close contacts will get infected with TB
Admitted: Airborne precautions(Air under negative pressure and is HEPA filtered before exhausted from room)
Contact tracing: hospital and community
Require 2 weeks of adequate therapy and 3 negative Respiratory samples (if original samples was AFB smear positive) before removal from Airborne precautions.
16. Diagnostic Testing Culture is still the recommended method for diagnosing TB
Detection of AFB in respiratory secretions
Chest X-ray
Tuberculin skin test (TST)
Molecular diagnostic tests: not yet sensitive enough
IGRA (Interferon gamma release assays): sensitized T-cells ? Latent TB detection
17. Canadian Data: MTB cases
18. Vaccine BCG vaccine (live M.bovis): protects from uncontrolled systemic spread ? up to 80% protection(ie. Doesn’t completely prevent risk of infection)
Used in countries where endemic TB poses significant risk
Canada: High risk groups ? Infants < 1 yr First Nations and Inuit communities (> 15 AFB smear positive pulmonary TB cases/100,000 pop)
19. Extra-pulmonary TB Risk of transmission minimal
Presentation can be confusing- testing may be delayed due to lack of suspicion about TB
Most common sites:- GI tract- Liver- Brain- Genito-Urinary tract
20. HIV: Risk of M.tuberculosis HIV patients at increased risk of TB- immunocompromised- First Nations HIV positive; drugs, crowded living conditions
Harder to treat TB in HIV patients
21. Drug resistant TB: More common in Foreign born Canadians TB drug resistance: resistant to one or more of first line drugs: isoniazid, rifampin, pyrazinamide and ethambutol (~ 5% in Canada)
MDR-TB: resistance to at least INH and rifampin (~ 0.7% in Canada)
XDR-TB: resistance to all first line therapeutic drugs (rare)
22. Summary of Key Issues: M. tuberculosis: - Acid Fast Bacilli (AFB)- Risk group 3 bacterium- Humans are the only reservoir
Pathogenesis: - Inhalation of infectious droplet nuclei- unrestricted replication ? spreads throughout body- Cell-mediated immune response - Granuloma formation ? latent infection- Reactivation if immunity wanes
Public Health Risk- Pulmonary TB highest risk for spread- HIV link- MDR: multi-drug resistant strains