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Anthrax

GMJ News knowledge hub · last reviewed September 2026 · Georgian Medical Journal

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Anthrax — caused by Bacillus anthracis — is both a natural zoonosis (causing approximately 1,000-2,000 human cases/year from contact with infected livestock) and a WHO Neglected Tropical Disease and CDC Category A bioterrorism agent, as demonstrated by the 2001 US anthrax letter attacks that killed 5 people and showed the potential for deliberate spore weaponisation (WHO). Three clinical forms of anthrax cause strikingly different presentations: cutaneous anthrax (most common — a characteristic black eschar); inhalation anthrax (most lethal — initially resembling influenza, progressing to mediastinal widening and death within days); and gastrointestinal anthrax (from eating undercooked infected meat). The Caucasus region including Georgia has documented anthrax in livestock, making occupational exposure relevant.

Key messages

Three clinical forms — bioterrorism and NTD
Anthrax causes three distinct clinical forms depending on exposure route: cutaneous (most common — characteristic black eschar); inhalation (most lethal — widened mediastinum, rapid death without treatment); and gastrointestinal. B. anthracis is a CDC Category A bioterrorism pathogen.
Spores — the key to danger
B. anthracis produces highly resistant spores that persist in soil for decades. Spores are the infectious form for humans — entering through skin abrasions, inhalation or ingestion. The 2001 anthrax letter attacks used refined spore powder to infect postal workers, politicians and media.
WHO NTD in endemic areas
Natural anthrax (zoonotic) remains endemic in parts of Africa, Central Asia, Southern Europe and the Americas — where soil spore contamination in grazing areas infects cattle, sheep and goats. The Caucasus/Central Asia has documented anthrax in livestock, making it relevant to Georgia.
Ciprofloxacin or doxycycline for 60 days
Anthrax treatment: ciprofloxacin (500mg BD) or doxycycline (100mg BD) — for 60 days total in inhalation anthrax (spores may persist in lungs). Anthrax antitoxin (raxibacumab, obiltoxaximab) reduces toxin-mediated damage in severe disease. Early treatment is critical.
B. anthracis toxins cause most pathology
B. anthracis produces three proteins that form two exotoxins: lethal toxin (LT — kills macrophages) and edema toxin (ET — promotes fluid accumulation). These toxins cause most of the pathology of anthrax — continuing to damage even when bacteria are killed by antibiotics.
Animal vaccination prevents human disease
Livestock vaccination in endemic areas — using live attenuated Sterne strain vaccines for animals — prevents human anthrax by eliminating the animal reservoir. Regular vaccination of at-risk livestock is the primary zoonotic prevention strategy.

Key statistics

1,000-2,000
naturally acquired anthrax cases/year globally
WHO
5
deaths in 2001 US anthrax letter attacks (22 cases)
CDC/History
80-90%
mortality of untreated inhalation anthrax
WHO
20%
mortality of untreated cutaneous anthrax
WHO
60 days
antibiotic duration for inhalation anthrax
WHO/CDC
Decades
B. anthracis spores survive in soil
WHO

Anthrax clinical forms — incidence, mortality and mechanism

Source: WHO. Cutaneous most common; inhalation most lethal; gastrointestinal from infected meat.

Glossary of key terms

Bacillus anthracis
WHO
A Gram-positive, spore-forming, rod-shaped bacterium — the causative agent of anthrax. Produces highly resistant endospores that persist in soil and on dried animal hides for decades to centuries. Virulence factors: two plasmids (pXO1 — encodes toxin; pXO2 — encodes capsule).
Anthrax lethal toxin (LT) and edema toxin (ET)
WHO/Research
Two exotoxins formed by combining a shared protective antigen (PA) with either lethal factor (LF) or edema factor (EF). LT: kills macrophages (causing immune evasion) and promotes septic shock. ET: adenylate cyclase that floods cells with cAMP, causing tissue edema and impairing immune function.
Inhalation anthrax (Woolsorter's disease)
WHO/CDC
Contracted by inhaling B. anthracis spores — historically in wool sorters handling contaminated animal hides; in bioterrorism settings, from weaponised spore aerosols. Biphasic: flu-like prodrome (2-5 days) → sudden deterioration with mediastinal widening, haemothorax, meningitis, septic shock. Mortality 80-90% without treatment; high even with treatment if started late.
Cutaneous anthrax
WHO
The most common form — spores enter skin through cuts/abrasions during contact with infected animals or hides. Pathognomonic lesion: painless papule → vesicle → central ulcer with black necrotic eschar surrounded by massive painless oedema. Untreated: approximately 20% mortality; with antibiotics, <1%.
Anthrax antitoxin
FDA/CDC
Raxibacumab (anti-PA mAb) and obiltoxaximab (anti-PA mAb) — approved by FDA for inhalation anthrax in combination with antibiotics. Neutralise protective antigen (PA) and prevent toxin formation. Used when clinical response to antibiotics alone appears insufficient.
B. anthracis as bioterrorism agent
CDC/WHO
B. anthracis is a Category A bioterrorism agent — the highest-priority because: it can be aerosolised; spores are stable; inhalation causes severe, potentially lethal disease; large quantities could be produced; it would cause widespread panic. The 2001 US anthrax letter attacks remain the most significant bioterrorism attack in US history.

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