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Bacillus Anthracis
Anthrax
INTRODUCTION
 Commonly known as "Bacteria of livestock''.
 The organism was first discovered by ROBERT KOCH.
 Bacillus anthracis is an agent of disease ANTHRAX.
 Occasionally infects humans.
 Known as the best weapon for bioterrorism.
 Mode of infection is through spores.
 Transmitted through inhalation, ingestion or
Contamination.
HISTORY
 First cases of cutaneous anthrax came from men
working with livestock was referred to as Wool
sorter's disease.
 Anthrax vaccine was approved in 1970.
 Largest outbreak of human anthrax was observed in
1978-1980.
STRUCTURE AND CHARACTERISTICS
 Gram positive.
 Non-motile.
 Facultative anaerobe.
 Rectangular rod shaped bacterium with square ends.
 Temperature range for optimum growth is 35-37 C
ENDOSPORE FORMATION
 Bacillus produces spores.
 It can remain inactive for years but can germinate after gaining entry inside host
body.
 Spores resist heat, drying, and disinfectants.
 Spores can gain entry inside body through
inhalation or wound.
INFECTION
 Can infect both cattle and human beings.
 Infection is caused through spores.
 Spores are transferred from animals to humans through respiration or any wound.
 One can be infected from soil and air too.
 Infection through wounds is called Cutaneous Infection.
 Infection through air is called Pulmonary infection.
 Eating raw meat can cause Gastrointestinal infection.
CYCLE OF ANTHRAX
TYPES OF ANTHRAX
CUTANEOUS ANTHRAX-
Bacteria enters through wound or other
parts of skin.
Chances are more than or equal to 95%.
Develops painless and dark lesions.
Invade nearest lymph nodes and enter
blood circulation.
Can cause septicemia.
TYPES OF ANTHRAX
PULMONARY ANTHRAX
Rare.
Mortality rate is 100%.
Inflammation of lymph nodes.
Infects respiratory system
including lungs.
Host becomes immunodeficient.
Mostly results into death.
TYPES OF ANTHRAX
GASTROINTESTINAL ANTHRAX
Caused by eating raw meat.
Spores are ingested.
Infects the mouth and intestinal
tract.
Oral and abdominal lesions are
observed.
PATHOGENICITY
MEDIATORS OF PATHOGENESIS
EXOTOXINS
1. Edema factor: produce
cAMP which results in
degradation.
2. Lethal toxin: responsible
for tissue necrosis.
3. Protective
antigen: facilitate entry
of EF & LT.
BACTERIAL CAPSULE
It is made up of peptidoglycan
or glycoproteins.
• It acts as a protective layer.
• Helps to prevent
immunological functions.
• This is a slimy layer which
prevents phagocytosis.
PATHOGENICITY
 There are always two strategies in pathogenesis:-
1. To go against host immune system which is done here with the help of
BACTERIAL CAPSULE.
2. To destroy the cell which in this case is done by EXOTOXINS.
CAPSULE
SYMPTOMS
CUTANEOUS ANTHRAX
Skin infection, itchy sores, swelling, scabs.
PULMONARY ANTHRAX
Fever, headache, cough, shortness of breath and
chest pain.
GASTROINTESTINAL ANTHRAX
Abdominal pain, bloody diarrhea, fever, mouth
sores, nausea and vomiting.
DIAGNOSIS
 GRAM STAINING- useful for cutaneous anthrax
 BLOOD SAMPLES- for checking the presence.
 SKIN LESIONS AND PUS - for cutaneous anthrax.
 RESPIRATORY SECRETIONS- for pulmonary anthrax.
 X RAY -pulmonary anthrax
 CT SCAN - inhalation infection.
 PCR – for detection of anthrax exotoxins.
 STOOL- intestinal anthrax.
CULTURED ON NUTRIENT/BLOOD AGAR at 37 degrees.
TREATMENT
CUTANEOUS ANTHRAX
Simple antibiotics can do the job. Doxycycline ,
erythromycin , ciprofloxacin are used.
PULMONARY ANTHRAX
Multidrug therapy is effective. Ciprofloxacin,
rifampin, vancomycin combination is used.
GASTROINTESTINAL ANTHRAX
Almost same antibiotics are used.
PREVENTION
Vaccination.
Early detection.
Air filters.
Keeping pets clean.
Pre antibiotic treatment.
Decontamination of exposed area.
THANK YOU

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Bacillus anthracis

  • 2. INTRODUCTION  Commonly known as "Bacteria of livestock''.  The organism was first discovered by ROBERT KOCH.  Bacillus anthracis is an agent of disease ANTHRAX.  Occasionally infects humans.  Known as the best weapon for bioterrorism.  Mode of infection is through spores.  Transmitted through inhalation, ingestion or Contamination.
  • 3. HISTORY  First cases of cutaneous anthrax came from men working with livestock was referred to as Wool sorter's disease.  Anthrax vaccine was approved in 1970.  Largest outbreak of human anthrax was observed in 1978-1980.
  • 4. STRUCTURE AND CHARACTERISTICS  Gram positive.  Non-motile.  Facultative anaerobe.  Rectangular rod shaped bacterium with square ends.  Temperature range for optimum growth is 35-37 C
  • 5. ENDOSPORE FORMATION  Bacillus produces spores.  It can remain inactive for years but can germinate after gaining entry inside host body.  Spores resist heat, drying, and disinfectants.  Spores can gain entry inside body through inhalation or wound.
  • 6.
  • 7. INFECTION  Can infect both cattle and human beings.  Infection is caused through spores.  Spores are transferred from animals to humans through respiration or any wound.  One can be infected from soil and air too.  Infection through wounds is called Cutaneous Infection.  Infection through air is called Pulmonary infection.  Eating raw meat can cause Gastrointestinal infection.
  • 9. TYPES OF ANTHRAX CUTANEOUS ANTHRAX- Bacteria enters through wound or other parts of skin. Chances are more than or equal to 95%. Develops painless and dark lesions. Invade nearest lymph nodes and enter blood circulation. Can cause septicemia.
  • 10. TYPES OF ANTHRAX PULMONARY ANTHRAX Rare. Mortality rate is 100%. Inflammation of lymph nodes. Infects respiratory system including lungs. Host becomes immunodeficient. Mostly results into death.
  • 11. TYPES OF ANTHRAX GASTROINTESTINAL ANTHRAX Caused by eating raw meat. Spores are ingested. Infects the mouth and intestinal tract. Oral and abdominal lesions are observed.
  • 12. PATHOGENICITY MEDIATORS OF PATHOGENESIS EXOTOXINS 1. Edema factor: produce cAMP which results in degradation. 2. Lethal toxin: responsible for tissue necrosis. 3. Protective antigen: facilitate entry of EF & LT. BACTERIAL CAPSULE It is made up of peptidoglycan or glycoproteins. • It acts as a protective layer. • Helps to prevent immunological functions. • This is a slimy layer which prevents phagocytosis.
  • 13. PATHOGENICITY  There are always two strategies in pathogenesis:- 1. To go against host immune system which is done here with the help of BACTERIAL CAPSULE. 2. To destroy the cell which in this case is done by EXOTOXINS. CAPSULE
  • 14. SYMPTOMS CUTANEOUS ANTHRAX Skin infection, itchy sores, swelling, scabs. PULMONARY ANTHRAX Fever, headache, cough, shortness of breath and chest pain. GASTROINTESTINAL ANTHRAX Abdominal pain, bloody diarrhea, fever, mouth sores, nausea and vomiting.
  • 15. DIAGNOSIS  GRAM STAINING- useful for cutaneous anthrax  BLOOD SAMPLES- for checking the presence.  SKIN LESIONS AND PUS - for cutaneous anthrax.  RESPIRATORY SECRETIONS- for pulmonary anthrax.  X RAY -pulmonary anthrax  CT SCAN - inhalation infection.  PCR – for detection of anthrax exotoxins.  STOOL- intestinal anthrax. CULTURED ON NUTRIENT/BLOOD AGAR at 37 degrees.
  • 16. TREATMENT CUTANEOUS ANTHRAX Simple antibiotics can do the job. Doxycycline , erythromycin , ciprofloxacin are used. PULMONARY ANTHRAX Multidrug therapy is effective. Ciprofloxacin, rifampin, vancomycin combination is used. GASTROINTESTINAL ANTHRAX Almost same antibiotics are used.
  • 17. PREVENTION Vaccination. Early detection. Air filters. Keeping pets clean. Pre antibiotic treatment. Decontamination of exposed area.