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MYCOBACTERIUM TUBERCULOSIS
Presented by:
Nida Akram
L1S17BSMR0005
Presented to:
Dr. Basit Zeshan
Faculty:
Life Sciences
University of Central Punjab, Lahore
DISCOVERY OF MYCOBACTERIUM TUBERCULOSIS
 Robert Koch
 German Scientist
 In 1882
 Father of Bacteriology
 Nobel Prize
CHARACTERISTICS OF MYCOBACTERIUM TUBERCULOSIS
 Obligate Aerobe
 Non motile
 Small Bacillus
 Does not produce spores
 Obligate intracellular parasite
 2-4 um in length
 0.2-0.5 um in width
 Divides every 16 to 20 hours
 Survive in dry states for weeks Electron scanning micrograph
CELL ENVELOPE STRUCTURE
 Closely related to Gram +ve Bacteria
 Unique lipid composition
 Thick waxy coat
 Plasma membrane
 Cell wall
 Lipid layers
 Other glycolipids
 Porins and proteins
CELL ENVELOPE STRUCTURE
 Cell wall:
 Peptidoglycan
 Arabinoglactan
 Layer sugar
 D-arabinose and D-glactose
 Links to peptidoglycan and lipid layers
 Provide additional strength
CELL ENVELOPE STRUCTURE
 Lipid layers:
 Cell envelope composed of unique lipid layer
 Important one is Mycolic acid
 Long chain fatty acids
 Covalently linked to Arabinoglactan
 Form thick waxy coat
 Low permeability
 Allow to show resistance to drying and chemical
disinfectants
CELL ENVELOPE STRUCTURE
 Other glycolipids:
 Variety of glycolipids
 Released from cell envelope
 Interact with other membranes or receptors
 Bioactive
 Porins:
 Move essential molecules into and out of cell
CULTURING
 Lowenstein Jensen media
 Cultivation and isolation
 Glycerated egg base medium
 Colonies:
 Brown
 Rough
 Dry and non pigmented
MICROSCOPY OF MYCOBACTERIUM TUBERCULOSIS
 Does not identify by Gram Staining
 High lipid contents (Mycolic acid)
 Acid fast stains:
 Ziehl Neelsan stain
 Florescent stain (Auramine)
 Cells are:
 Curved
 Rod shaped
 Wrapped together
 Neither gram negative nor gram positive
MICROSCOPY OF MYCOBACTERIUM
TUBERCULOSIS
 Ziehl Neelsan Stain:
 Composition:
 Carbol Fuchsine
 Acid Alcohol
 Methylene blue
 Procedure
 Bacteria will appear bright red
MICROSCOPY OF MYCOBACTERIUM
TUBERCULOSIS
 Fluorescent Stain:
 Auramine Phenol stain
 Clinical microbiology
 Bacteria appear greenish yellow
 More rapid method than ZN technique
 Method:
 Smear stained with Auramine phenol
 Rinse with water
 Decolorize in acid alcohol
 Counterstain with 0.1% Potassium Permanganate
 Rinse and air dry
 40X Objective is used
CAUSATIVE AGENT OF TB
 Mycobacterium tuberculosis
 A type of Mycobacterium
 Main cause
 Mycobacterium Tuberculosis Complex
 M.bovis
 M.avium
 M.tuberculosis
WHAT IS TUBERCULOSIS??
 Contagious infection that
usually attacks the lungs. It
can also spread to other
parts of the body like brain,
kidneys and spine.
TYPES OF TUBERCULOSIS
 Latent TB:
 Germs stops by immune system
 No symptoms
 Patient is not contagious
 Infection is still alive
 Can become active
 Inactive TB
 Resembles with chickenpox infection
TYPES OF TUBERCULOSIS
 Active TB
 Germs multiply
 Patient become sick
 Disease spread from patient to others
 90% of active TB cases are from reactivation of Latent TB
infection.
PATHOGENESIS OF MYCOBACTERIUM
TUBERCULOSIS
 Bacteria recognize as invaders in alveoli
 Attacked by macrophages
 Not all bacteria destroyed
 hijack macrophages
 Increasing population
 Bursting of macrophages
 Granuloma
 Necrotization of granuloma
 Mixture of blood and sputum
 Lungs fill with clusters of bacteria
Mycobacterium tuberculosis

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Mycobacterium tuberculosis

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  • 2. MYCOBACTERIUM TUBERCULOSIS Presented by: Nida Akram L1S17BSMR0005 Presented to: Dr. Basit Zeshan Faculty: Life Sciences University of Central Punjab, Lahore
  • 3. DISCOVERY OF MYCOBACTERIUM TUBERCULOSIS  Robert Koch  German Scientist  In 1882  Father of Bacteriology  Nobel Prize
  • 4. CHARACTERISTICS OF MYCOBACTERIUM TUBERCULOSIS  Obligate Aerobe  Non motile  Small Bacillus  Does not produce spores  Obligate intracellular parasite  2-4 um in length  0.2-0.5 um in width  Divides every 16 to 20 hours  Survive in dry states for weeks Electron scanning micrograph
  • 5. CELL ENVELOPE STRUCTURE  Closely related to Gram +ve Bacteria  Unique lipid composition  Thick waxy coat  Plasma membrane  Cell wall  Lipid layers  Other glycolipids  Porins and proteins
  • 6. CELL ENVELOPE STRUCTURE  Cell wall:  Peptidoglycan  Arabinoglactan  Layer sugar  D-arabinose and D-glactose  Links to peptidoglycan and lipid layers  Provide additional strength
  • 7. CELL ENVELOPE STRUCTURE  Lipid layers:  Cell envelope composed of unique lipid layer  Important one is Mycolic acid  Long chain fatty acids  Covalently linked to Arabinoglactan  Form thick waxy coat  Low permeability  Allow to show resistance to drying and chemical disinfectants
  • 8. CELL ENVELOPE STRUCTURE  Other glycolipids:  Variety of glycolipids  Released from cell envelope  Interact with other membranes or receptors  Bioactive  Porins:  Move essential molecules into and out of cell
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  • 10. CULTURING  Lowenstein Jensen media  Cultivation and isolation  Glycerated egg base medium  Colonies:  Brown  Rough  Dry and non pigmented
  • 11. MICROSCOPY OF MYCOBACTERIUM TUBERCULOSIS  Does not identify by Gram Staining  High lipid contents (Mycolic acid)  Acid fast stains:  Ziehl Neelsan stain  Florescent stain (Auramine)  Cells are:  Curved  Rod shaped  Wrapped together  Neither gram negative nor gram positive
  • 12. MICROSCOPY OF MYCOBACTERIUM TUBERCULOSIS  Ziehl Neelsan Stain:  Composition:  Carbol Fuchsine  Acid Alcohol  Methylene blue  Procedure  Bacteria will appear bright red
  • 13. MICROSCOPY OF MYCOBACTERIUM TUBERCULOSIS  Fluorescent Stain:  Auramine Phenol stain  Clinical microbiology  Bacteria appear greenish yellow  More rapid method than ZN technique  Method:  Smear stained with Auramine phenol  Rinse with water  Decolorize in acid alcohol  Counterstain with 0.1% Potassium Permanganate  Rinse and air dry  40X Objective is used
  • 14. CAUSATIVE AGENT OF TB  Mycobacterium tuberculosis  A type of Mycobacterium  Main cause  Mycobacterium Tuberculosis Complex  M.bovis  M.avium  M.tuberculosis
  • 15. WHAT IS TUBERCULOSIS??  Contagious infection that usually attacks the lungs. It can also spread to other parts of the body like brain, kidneys and spine.
  • 16. TYPES OF TUBERCULOSIS  Latent TB:  Germs stops by immune system  No symptoms  Patient is not contagious  Infection is still alive  Can become active  Inactive TB  Resembles with chickenpox infection
  • 17. TYPES OF TUBERCULOSIS  Active TB  Germs multiply  Patient become sick  Disease spread from patient to others  90% of active TB cases are from reactivation of Latent TB infection.
  • 18. PATHOGENESIS OF MYCOBACTERIUM TUBERCULOSIS  Bacteria recognize as invaders in alveoli  Attacked by macrophages  Not all bacteria destroyed  hijack macrophages  Increasing population  Bursting of macrophages  Granuloma  Necrotization of granuloma  Mixture of blood and sputum  Lungs fill with clusters of bacteria