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Sporogenous Bacilli
Aerobic Bacilli

1.Bacillus anthracis
2.Bacillus cereus
3. Anthracoid bacilli

Anaerobic Clostridia

1. Cl.perfringens
2. Cl. tetani
3. Cl.botulinum
-First pathogenic bacteria to be observed under microscope
-First bacilli to be isolated in pure culture
-First bacilli in which spores were demonstrated
-First bacterium used for preparation of attenuated vaccine
-First bacterium to be shown cause of disease
-First bacterium that evolved as a potent weapon in bioterrorism
Morphology
Cultural characteristics

Biochemical reactions
Resistance
Pathogenicity
Lab diagnosis
Epidemiology
Prophylaxis
Treatment

BIOTERRORISM
-One of the largest pathogenic bactera;4-8x1-1.5 mm in size
-Gram +ve, rod shaped, non-motile and non acid-fast
-Bamboo stick appearance of long chains
-Polypeptidal capsule
-Central or sub terminal oval spores
-Aerobic ,Facultative anaerobic
-On NA : Colonies are round, grayish white,irregular,raised
with “frosted glass” appearance,2-3 mm in diameter.
Medusa head /Barrister's wig appearance of colonies under
low magnification
-On BA: Non-hemolytic colonies
-Gelatin stab culture: “Inverted fir tree" appearance
-PLET medium: for selective isolation
-Glucose, Maltose, Sucrose fermented with ACID production
-Nitrate reduction test
-Gelatin liquefaction test

All positive

-Catalase test

RESISTANCE

-Spores survive for many years(dry state & soil)
-vegetative cells 60 0C x 30 min.
-spores 1000C x 10 min.
-4% FD & KMnO4 kills spores
Duckering: 2% formaldehyde at 30-40 0C for 20 min. disinfects
wool & 0.25% at 60 0C for 6 hrs. for animal hair & bristles.
-Moist heat kills :
Virulence factors:
1.Capsular polypeptide – inhibits phagocytosis
2.Anthrax toxin –a complex of 3 fractions:
-Edema factor(OF or Factor I)
whole complex
-Protective antigen factor(PA or Factor II) produces local edema
-Lethal factor(LF or Factor III)
& generalized shock

Edema factor + protective antigen = Edema toxin
Lethal factor + protective antigen = Lethal toxin
Clinically three forms of Human anthrax occur
1.Cutaneous anthrax
2.Pulmonary anthrax
3.Intestinal anthrax
Broadly can be classified into
Non Industrial/Agricultural ( Through infected animals):
Cutaneous anthrax
Rarely intestinal anthrax
Industrial Anthrax ( Through animal products):

Mostly through animal products( wools, hair, hides, bones)
Likely to develop Cutaneous and pulmonary anthrax
1.Cutaneous Anthrax(95-99% human anthrax)
•Mainly in professionals( Veterinarian, butcher, Zoo keepers,

persons handling carcasses/hides/hair, loading skin on bare
backs-hide porters disease .
• Spores infect skin- a characteristic gelatinous edema &

congestion develops at the site (Papule- pustule-black
ulcer(eschar) .Later a ring of vesicle containing serous fluid
surrounds eschar termed as Malignant pustule.
•Face ,neck,arms and back are common sites
• 80-90% heal spontaneously ( 2-6wks)
• 10-20% progressive disease – develop fatal septicemia, death
Different locations & morphology of lesion in cutaneous anthrax
2.Pulmonar Anthrax- wool sorter's/Ragpicker’s disease:
-Acquired with inhalation of spores(bioterrorism-aerosol)
-Requires very high infective dose(10,000 t0 20,000 spores)

-Inflammatory reaction occurs in trachea, bronchi with

hemorrhagic bronchospasm
-Presents initially with non -specific symptoms but later
with symptoms of severe respiratory infection & severe
respiratory collapse
-Hemorrhagic meningitis sometimes occurs as complication
-Progress to septicemia very rapidly
-Mortality rate is very high
3.Intestinal Anthrax

-Rare in man and is found in primitive communities eating
dead carcasses of infected animal
-Presents with serious severe enteritis, bloody or hemorrhagic
diarrhoea,bloody vomit
-Fatality rate is 25-60% depending upon treatment
EPIDEMIOLOGY(INDIA)
-Anthrax is enzootic in India
-An epizootic of anthrax in sheep active AP,TN borders
-Largest live stock population in the world

-Pondicherry ( JIPMER) - 30 human cases reported ( Mostly
Cutaneous, Septicemic or Meningeal)

-Vellore ( CMC)- 49 human cases
-Chittor ( Rajasthan)- 30 human cases
-Tirupati ( Andhrapradesh)- 25 human cases
-Midnapur ( WB)- 22 human cases
LABORATORY DIAGNOSIS
A. Hematological investigation-not significant
B.Bacteriological investigation:
Specimen- swabs, pus, pustules, blood ,sputum, feces etc.
1.Microscopy:Gram staining & spore staining
Characteristic Mc’ Fadyean’s reaction
Immunofluorescent microscopy
2.Culture: Suitable culture media for selective isolation
3.Animal inoculation : done in guinea pigs, mice & rabbits.
3.Serology(Ascoli’s thermoprecipitation test)
4.Molecular methods : PCR with specific primers
5.Molecular typing: MLVA & AFLL for epidemiological studies
PROPHYLAXIS
Humans protected by preventing disease in animals

-Veterinary supervision
-Trade restrictions
-Proper sterilization & disinfection of animal products
-Deep burial or cremation of carcasses
 Improved industry standards
 Safety practices in laboratories
 Post-exposure antibiotic prophylaxis
VACCINATION:
-Active immunization with Pasteur’s anthrax vaccine
-Salvo immune serum in serious toxic cases
-Cell free vaccine in high risk groups
-Inactivated /killed vaccine for veterinarians & Agri-workers
-Sterne vaccine used effectively in livestock's
-Alum precipitated toxoid found safe in professionals
 3 doses given intramuscularly
TREATMENT
Effective antibiotics in humans:
Sulphonamides,ciprofloxacin,penicillin,erythromycin,
Vancomycin,doxycyline,chloramphenicol
FDA -approved ciprofloxacin,doxycycline and penicillin
BIOTERRORISM-anthrax as a bioweapon
-Anthrax was used by Scandinavian rebels against Russians
-Operation vegetarian by Royal Air Force against Germany in
1944 ,an anti-livestock operation
-In 1997-accidental release of anthrax spores from biological
weapons complex in Russia infected 94 people ,68 died
-In Oct.2001 anthrax attacks in USA termed Amerithrax(FBI)
22 cases- 11 inhalation(5 deaths),11 cutaneous(no deaths)
-Important cause of food poisoning
-Distributed widely in nature(soil, vegetables & foods)
-Non-Capsulated but Motile (few non-motile strains )
-Two patterns of food borne disease are produced:
1.Diarrhoeal type: -caused by serotypes 2,6,8,9,10 & 12
-associated with wide range of foods
-characterized by diarrhea & abdominal pain
2.Emetic type(fried rice syndrome) caused by STs 1,3 & 5
- associated with consumption of cooked rice
- characterized by acute nausea & vomiting
For isolation MYPA medium is used
10,00000 bacilli/gram of stool is significant
ANTHRACOIS /PSEUDOANTHRAX
-Saprophytic ,spore-forming, non-pathogenic species
-They are most common laboratory contaminants
(e.g. B.subtilis contaminating blood transfusion bottles
-They are opportunistic & may cause septicemia
Bacillus anthrax ,a potent bioweapon
Bacillus anthrax ,a potent bioweapon
Bacillus anthrax ,a potent bioweapon
Bacillus anthrax ,a potent bioweapon

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Bacillus anthrax ,a potent bioweapon

  • 1.
  • 2. Sporogenous Bacilli Aerobic Bacilli 1.Bacillus anthracis 2.Bacillus cereus 3. Anthracoid bacilli Anaerobic Clostridia 1. Cl.perfringens 2. Cl. tetani 3. Cl.botulinum
  • 3. -First pathogenic bacteria to be observed under microscope -First bacilli to be isolated in pure culture -First bacilli in which spores were demonstrated -First bacterium used for preparation of attenuated vaccine -First bacterium to be shown cause of disease -First bacterium that evolved as a potent weapon in bioterrorism
  • 4. Morphology Cultural characteristics Biochemical reactions Resistance Pathogenicity Lab diagnosis Epidemiology Prophylaxis Treatment BIOTERRORISM
  • 5. -One of the largest pathogenic bactera;4-8x1-1.5 mm in size -Gram +ve, rod shaped, non-motile and non acid-fast -Bamboo stick appearance of long chains -Polypeptidal capsule -Central or sub terminal oval spores
  • 6. -Aerobic ,Facultative anaerobic -On NA : Colonies are round, grayish white,irregular,raised with “frosted glass” appearance,2-3 mm in diameter. Medusa head /Barrister's wig appearance of colonies under low magnification -On BA: Non-hemolytic colonies -Gelatin stab culture: “Inverted fir tree" appearance -PLET medium: for selective isolation
  • 7. -Glucose, Maltose, Sucrose fermented with ACID production -Nitrate reduction test -Gelatin liquefaction test All positive -Catalase test RESISTANCE -Spores survive for many years(dry state & soil) -vegetative cells 60 0C x 30 min. -spores 1000C x 10 min. -4% FD & KMnO4 kills spores Duckering: 2% formaldehyde at 30-40 0C for 20 min. disinfects wool & 0.25% at 60 0C for 6 hrs. for animal hair & bristles. -Moist heat kills :
  • 8. Virulence factors: 1.Capsular polypeptide – inhibits phagocytosis 2.Anthrax toxin –a complex of 3 fractions: -Edema factor(OF or Factor I) whole complex -Protective antigen factor(PA or Factor II) produces local edema -Lethal factor(LF or Factor III) & generalized shock Edema factor + protective antigen = Edema toxin Lethal factor + protective antigen = Lethal toxin
  • 9.
  • 10. Clinically three forms of Human anthrax occur 1.Cutaneous anthrax 2.Pulmonary anthrax 3.Intestinal anthrax Broadly can be classified into Non Industrial/Agricultural ( Through infected animals): Cutaneous anthrax Rarely intestinal anthrax Industrial Anthrax ( Through animal products): Mostly through animal products( wools, hair, hides, bones) Likely to develop Cutaneous and pulmonary anthrax
  • 11. 1.Cutaneous Anthrax(95-99% human anthrax) •Mainly in professionals( Veterinarian, butcher, Zoo keepers, persons handling carcasses/hides/hair, loading skin on bare backs-hide porters disease . • Spores infect skin- a characteristic gelatinous edema & congestion develops at the site (Papule- pustule-black ulcer(eschar) .Later a ring of vesicle containing serous fluid surrounds eschar termed as Malignant pustule. •Face ,neck,arms and back are common sites • 80-90% heal spontaneously ( 2-6wks) • 10-20% progressive disease – develop fatal septicemia, death
  • 12. Different locations & morphology of lesion in cutaneous anthrax
  • 13. 2.Pulmonar Anthrax- wool sorter's/Ragpicker’s disease: -Acquired with inhalation of spores(bioterrorism-aerosol) -Requires very high infective dose(10,000 t0 20,000 spores) -Inflammatory reaction occurs in trachea, bronchi with hemorrhagic bronchospasm -Presents initially with non -specific symptoms but later with symptoms of severe respiratory infection & severe respiratory collapse -Hemorrhagic meningitis sometimes occurs as complication -Progress to septicemia very rapidly -Mortality rate is very high
  • 14. 3.Intestinal Anthrax -Rare in man and is found in primitive communities eating dead carcasses of infected animal -Presents with serious severe enteritis, bloody or hemorrhagic diarrhoea,bloody vomit -Fatality rate is 25-60% depending upon treatment
  • 15.
  • 16. EPIDEMIOLOGY(INDIA) -Anthrax is enzootic in India -An epizootic of anthrax in sheep active AP,TN borders -Largest live stock population in the world -Pondicherry ( JIPMER) - 30 human cases reported ( Mostly Cutaneous, Septicemic or Meningeal) -Vellore ( CMC)- 49 human cases -Chittor ( Rajasthan)- 30 human cases -Tirupati ( Andhrapradesh)- 25 human cases -Midnapur ( WB)- 22 human cases
  • 17. LABORATORY DIAGNOSIS A. Hematological investigation-not significant B.Bacteriological investigation: Specimen- swabs, pus, pustules, blood ,sputum, feces etc. 1.Microscopy:Gram staining & spore staining Characteristic Mc’ Fadyean’s reaction Immunofluorescent microscopy
  • 18. 2.Culture: Suitable culture media for selective isolation 3.Animal inoculation : done in guinea pigs, mice & rabbits. 3.Serology(Ascoli’s thermoprecipitation test) 4.Molecular methods : PCR with specific primers 5.Molecular typing: MLVA & AFLL for epidemiological studies
  • 19. PROPHYLAXIS Humans protected by preventing disease in animals -Veterinary supervision -Trade restrictions -Proper sterilization & disinfection of animal products -Deep burial or cremation of carcasses  Improved industry standards  Safety practices in laboratories  Post-exposure antibiotic prophylaxis
  • 20. VACCINATION: -Active immunization with Pasteur’s anthrax vaccine -Salvo immune serum in serious toxic cases -Cell free vaccine in high risk groups -Inactivated /killed vaccine for veterinarians & Agri-workers -Sterne vaccine used effectively in livestock's -Alum precipitated toxoid found safe in professionals  3 doses given intramuscularly TREATMENT Effective antibiotics in humans: Sulphonamides,ciprofloxacin,penicillin,erythromycin, Vancomycin,doxycyline,chloramphenicol FDA -approved ciprofloxacin,doxycycline and penicillin
  • 21. BIOTERRORISM-anthrax as a bioweapon -Anthrax was used by Scandinavian rebels against Russians -Operation vegetarian by Royal Air Force against Germany in 1944 ,an anti-livestock operation -In 1997-accidental release of anthrax spores from biological weapons complex in Russia infected 94 people ,68 died -In Oct.2001 anthrax attacks in USA termed Amerithrax(FBI) 22 cases- 11 inhalation(5 deaths),11 cutaneous(no deaths)
  • 22. -Important cause of food poisoning -Distributed widely in nature(soil, vegetables & foods) -Non-Capsulated but Motile (few non-motile strains ) -Two patterns of food borne disease are produced: 1.Diarrhoeal type: -caused by serotypes 2,6,8,9,10 & 12 -associated with wide range of foods -characterized by diarrhea & abdominal pain 2.Emetic type(fried rice syndrome) caused by STs 1,3 & 5 - associated with consumption of cooked rice - characterized by acute nausea & vomiting For isolation MYPA medium is used 10,00000 bacilli/gram of stool is significant
  • 23. ANTHRACOIS /PSEUDOANTHRAX -Saprophytic ,spore-forming, non-pathogenic species -They are most common laboratory contaminants (e.g. B.subtilis contaminating blood transfusion bottles -They are opportunistic & may cause septicemia