ANTHRAX

• The anthrax bacillus, Bacillus anthracis, was the first

bacterium shown to be the cause of a disease- Koch’s
Postulate

• In 1877, Robert Koch grew the organism in pure culture,

demonstrated its ability to form endospores, and
produced experimental anthrax by injecting it into
animals.

• Anthrax is a disease of domesticated and wild animals

• Men suffer from anthrax occasionally due to close

contact with infected animal or animal products
 Bacillus anthracis
• Gram positive rods

• Capsulated ( Protein) – Capsule form in animal tissue and in special

laboratory condition ( 5% CO2)

• Forms endospore, centrally located, do not form in animal tissues

• MacFadyean ( Polychrome methylene blue) stain blue bacilli

with purple capsule

• Aerobic/ Facultative anerobe

•
Robert Koch's original micrographs of the anthrax bacillus

BImal K Das, Microbiology, AIIMS

Bacillus anthracis. Gram stain. The cells have characteristic
squared ends. The endospores are ellipsoidal shaped and located
centrally in the sporangium. The spores are highly refractile to
light and resistant to staining. BImal K Das, Microbiology, AIIMS
 Epiedemiology
• Distribution worldwide

• Not common in West. Common in Africa ( Zimbabwe),

S.E. Asia, China, South America, Turkey, Pakistan, India

• Human to human or animal to animal transmission is rare

( not contagious)

•Grazing animals become infected through ingestion of

spores in the soil ( Carcasses become the source)

Epidemic : A. Spread to contiguous geographic areas by

infected animal
B. Non contiguous geographic areas by
- biting flies ( Zimbabwe)
- Contaminated surface water pool
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 Pathogenesis
Endospores
(Abrasion, inhalation, ingestion)

Death Introduced

Septicemia Phagocytosed by Macrophages

10 7 to 10 8/ml Regional LNs

Blood stream

Multiply in Lymphatics Germinate inside Macrophages

Release

Vegetative Forms
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 Clinically three forms of Human anthrax occur

A. Cutaneous anthrax
B. Pulmonary anthrax
C. 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 ( inhalation)

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 Cutaneous Anthrax

• Mainly in professionals( Veterinarian, butcher, Zoo keeper

• Spores infect skin- a characteristic gelatinous edema develops at the

site (Papule- Vesicle-Malignant Pustule- Necrotic ulcer)

• 80-90% heal spontaneously ( 2-6wks)

• 0-20% progressive disease – develop septicemia

• 95-99% of all human anthrax occur as cutaneous anthrax

Intestinal Anthrax

• Due to in ingestion of infected carcasses

• Mucosal lesion to the lymphatic system

• Rare in developed countries

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• Extremely high mortality rate
 PULMONARY ANTHRAX

• Require very high infective dose ( > 10,000 spores)

• Acquired through inhalation of spores ( Bioterrorism - aerosol)

• Present with symptoms of severe respiratory infection( High fever &

Chest pain)

• Haemorrhagic mediastinitis

• Progress to septicemia very rapidly

• 10 7 to 10 9 bacilli/ ml of blood at the time of death

• Mortality rate is very high > 95%

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Meningitis

Meningitis has been reported in association with cutaneous, inhalation,

and gastrointestinal anthrax cases

About one-half of patients with inhalation anthrax will develop

hemorrhagic meningitis
 DIFFERENTIAL DIAGNOSIS OF ANTHRAX

CUTANEOUS ANTHRAX

Boils, Erysipelas, Cutaneous TB, Leprosy, Plague, Vaccinia, Rickettsial pox,

tularemia

INTESTINAL ANTHRAX

Typhoid fever, Acute Gastroenteritis, Tularemia, Peritonitis, Peptic ulcer,

Mechanical obstruction

PULMONARY ANTHRAX

Viral pneumonia, Mycoplasma. Psittacosis, Legionnaires disease, Q fever,

Histoplasmosis, Coccidiodomycosis, Silicosis, Sarcoidosis

Meningeal Anthrax : Sometime manifest as meningitis

D/D : Bacterial meningitis

Aseptic meningitis
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 VIRULENCE FACTORS

Anthrax Toxin – Complex of proteins ( all the components thermolabile)

A. Protective antigen
B. Edema factor
C. Lethal Factor

Protein capsule – Poly D Glutamic acid capsule

- Inhibits phagocytosis ( Unencapsulated strains –
nonpathogenic)
 LABORATORY DIAGNOSIS
Few points to remember

• Anthrax is not highly contagious

• Cutaneous anthrax is not lethal and is readily treated with
common antibiotics
• ID for human pulmonary / intestinal infection is > 10,000 spores

SPECIMEN TO COLLECT ( HUMAN ANTHRAX)

Disposable gloves, masks, overalls, boots, head gear and dust mask
Disposable items – Autoclave and incinerate

Cutaneous anthrax: Vesicular exudate – swabs and capillary tube aspirate

Intestinal anthrax: - Stool sample - isolate – guinea pig inoculation

- Blood( venipuncture) smear examination for bacilli
- Peritoneal fluid for culture
- Paired sera for Ab

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Pulmonary anthrax:

Specimens of blood obtained prior to antimicrobial therapy should be sent

for routine culture and for polymerase chain reaction (PCR) testing at a
Laboratory Response Network (LRN) laboratory

Pleural fluid, if present, for Gram stain, culture, and PCR

Cerebrospinal fluid, in patients with meningeal signs, for Gram stain,

culture, and PCR

Acute and convalescent serum samples for serologic testing

Pleural and/or bronchial biopsies for immunohistochemistry, if other tests

are negative
 SAMPLES FROM ANIMAL

Sudden death of animal in areas where anthrax was reported earlier

Carcasses 1 or 2 day old

Aspirate blood - MacFadyean stain for bacilli
Direct demonstration by IFA
Direct plating on blood agar

Putrefying carcasses
Blood, tissue and hide
Culture on selective medium
Soil sample from the areas where the carcass as lying

Serological assay

ELISA: based on anthrax toxin ( PA, LF and EF) for routine confirmation
and vaccine response)
Molecular techniques ( Only in the referral laboratories):
- RFLP
- PCR Fingerprinting
Animal Inoculation: Guinea pig and mice inoculation

Culture is confirmed by gamma phage lysis ( PlyG lysin enzyme- g phage)

 TREATMENT
Antibiotics should be given to unvaccinated individuals exposed to inhalation
anthrax.

Penicillin, tetracyclines and fluoroquinolones are effective if administered before the

onset of lymphatic spread or septicemia

Antibiotic treatment is effective in cutaneous anthrax

Inhalation anthrax can be effectively treated with antibiotics administered prior to

lymphatic spread or septicemia

INITIAL THERAPY OPTIMAL THERAPY

Adults Ciproflox Penicillin G 4 mu iv qdsX60days

( 400mg iv BDX60days) Doxycycline 100mg iv BDX60 days

Children Ciproflox
20-30mg/kgbodywt ivX60days Penicllin G 50,000 u/kg X 60 days

Alternatives – Amox, Tetracycline, Chloramphenicol, Erythromycin, Streptomycin

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Although initial therapy should be intravenous, patients may
be switched to oral therapy once they are stable, usually
after 14 to 21 days of intravenous therapy.

A total duration of treatment of 60 days (combination of

intravenous and oral therapy) should be given
 Vaccine against Anthrax

Killed bacilli and/or capsular antigens produce no significant immunity.

A nonencapsulated toxigenic strain (Sterne Strain) has been used effectively in

livestock.

Vaccine for humans: ( avirulent and nonencapsulated) sublethal amounts of the toxin
produced

Licensed in the U.S. is a preparation of the protective antigen (PA)

Dose: A. 3 doses subcutaneously at the interval of 2 wks

B. Followed by three additional doses at 6,12 and 18 months
C. Annual booster dose

Who are to be vaccinated

- Professionals ( Veternarians, butcher, Zoo keeper, Wild life workers, Forest guards)
- Military personnels

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 Anthrax and Biological Warfare

Countries > 10 countries in the world

Clouds of spores of Anthrax bacilli – aerosol ( war heads filled with anthrax spores)
- Through dried spores in envelops
September 9/11 WTO attack
Postal workers affected – Inhalation anthrax ( 40% mortality)
US – Columbia, Florida, New Jersey, N. York
Other parts of the world

BImal K Das, Microbiology, AIIMS