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Mycobacteria are slender rod
bacteria that stained with special
differential stains (Ziehl-Neelsen).
the most important mycobacteria
are the tuberculosis bacteria (TB)M.
tuberculosis and M. bovis and the
leprosy pathogen (LB) M.leprae
Morphology and culturing
 TB are slender, acid-fast
rods, nonsporing and
nonmotile.
They can be stained with
special agents (Ziehl-Neelsen
Ziehl-Neelsen staining of a urine
preparation
Culture of M. tuberculosis on
egg nutrient substrate according to
Lo¨wenstein-Jensen: after four weeks
of incubation rough, yellowish,
cauliflowerlike colonies.
Glycolipids and wax D
 Responsible for resistance to chemical
and physical effect.
 Adjuvant effect (wax D), i.e.,
enhancement of antigen immunogenicity.
 Intracellular persistence in nonactivated
macrophages by means of inhibition of
phagosome-lysosome fusion.
 — Complement resistance.
 — Virulencefactor
Tuberculin Test : Partially
purified tuberculin contains a
mixture of small proteins(10
kDa) is used to test for TB
exposure.
Delayed allergic reaction.
Microscopy: Ziehl-Neelsen
and/or auramine fluorescent
staining ,this method produces
rapid results but has a low level
of sensitivity
 Culture: on special solid and in
special liquid mediums time
require four to eight weeks.
Direct identification in patient
material.
 Molecular methods used for
direct detection of the M.
tuberculosis complex in
(uncultured) test material.
Morphology and culture.
Mycobacterium leprae (Hansen,
1873) is the causative
pathogen of leprosy. In morphological
terms, these acid-fast rods are
Identical to tuberculosis bacteria.
They differ, however, in that they
cannot be grown on nutrient
mediums or in cell cultures.
Pathogenesis. The pathological
mechanisms of LB are identical to
those of TB.
The host organism attempts to localize
and isolate infection foci by forming
granulomas.
Leprous granulomas are
histopathologically identical to
tuberculous granulomas.
 High counts of leprosy bacteria are
often found in the macrophagesof the
granulomas.
Immunity: The immune
defenses mobilized against a
leprosy infection are strictly
of the cellular type.
 The lepromin skin test can
detect a postinfection
allergy.
Diagnosis :Detection of the
pathogens in skin or nasal
mucosa scrapings under the
microscope using Ziehl-Neelsen
staining
(Molecular confirmation of DNA
sequences specific to leprosy
bacteria in a polymerase chain
reaction is possible (PCR).
Therapy: are treated with
dapson plus rifampicin for six
months.
 In lepromatous leprosy, nodular dermal and
mucosal lesions develop.
 Nerve inflammation and neuroparalysis will
follow, eventually resulting in mutilations
THANKS

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Mycobacteria

  • 1.
  • 2. Mycobacteria are slender rod bacteria that stained with special differential stains (Ziehl-Neelsen). the most important mycobacteria are the tuberculosis bacteria (TB)M. tuberculosis and M. bovis and the leprosy pathogen (LB) M.leprae
  • 3. Morphology and culturing  TB are slender, acid-fast rods, nonsporing and nonmotile. They can be stained with special agents (Ziehl-Neelsen
  • 4. Ziehl-Neelsen staining of a urine preparation Culture of M. tuberculosis on egg nutrient substrate according to Lo¨wenstein-Jensen: after four weeks of incubation rough, yellowish, cauliflowerlike colonies.
  • 5. Glycolipids and wax D  Responsible for resistance to chemical and physical effect.  Adjuvant effect (wax D), i.e., enhancement of antigen immunogenicity.  Intracellular persistence in nonactivated macrophages by means of inhibition of phagosome-lysosome fusion.  — Complement resistance.  — Virulencefactor
  • 6. Tuberculin Test : Partially purified tuberculin contains a mixture of small proteins(10 kDa) is used to test for TB exposure. Delayed allergic reaction.
  • 7. Microscopy: Ziehl-Neelsen and/or auramine fluorescent staining ,this method produces rapid results but has a low level of sensitivity  Culture: on special solid and in special liquid mediums time require four to eight weeks.
  • 8. Direct identification in patient material.  Molecular methods used for direct detection of the M. tuberculosis complex in (uncultured) test material.
  • 9. Morphology and culture. Mycobacterium leprae (Hansen, 1873) is the causative pathogen of leprosy. In morphological terms, these acid-fast rods are Identical to tuberculosis bacteria. They differ, however, in that they cannot be grown on nutrient mediums or in cell cultures.
  • 10. Pathogenesis. The pathological mechanisms of LB are identical to those of TB. The host organism attempts to localize and isolate infection foci by forming granulomas. Leprous granulomas are histopathologically identical to tuberculous granulomas.  High counts of leprosy bacteria are often found in the macrophagesof the granulomas.
  • 11. Immunity: The immune defenses mobilized against a leprosy infection are strictly of the cellular type.  The lepromin skin test can detect a postinfection allergy.
  • 12.
  • 13. Diagnosis :Detection of the pathogens in skin or nasal mucosa scrapings under the microscope using Ziehl-Neelsen staining (Molecular confirmation of DNA sequences specific to leprosy bacteria in a polymerase chain reaction is possible (PCR).
  • 14. Therapy: are treated with dapson plus rifampicin for six months.
  • 15.  In lepromatous leprosy, nodular dermal and mucosal lesions develop.  Nerve inflammation and neuroparalysis will follow, eventually resulting in mutilations