Bacillus anthracis


TAXONOMY

  • Domain: Bacteria

  • Phylum: Bacillota

  • Class: Bacilli

  • Order: Bacillales

  • Family: Bacillaceae

  • Genus: Bacillus

  • Species: B. anthracis

MORPHOLOGY

  • Gram‑positive, rod‑shaped bacterium measuring roughly 3–5 μm long and 1–1.2 μm wide

  • Forms long chains with blunt ends often described as “boxcar” or “bamboo stick”; colonies on agar are large, white or cream, and slimy due to the capsule.

  • Each cell forms one oval, centrally located endospore; spores are extremely resistant to heat, cold, radiation and desiccation.

  • Requires oxygen to sporulate and produces a poly‑D‑γ‑glutamic acid capsule around vegetative cells that shields it from phagocytosis.

  • Spores can persist dormant in soil for decades, emerging only when conditions are favourable

NOTABLE TRAITS

  • Virulence depends on two plasmids: pXO2, which encodes the capsule, and pXO1, which encodes the tripartite anthrax toxin.

    • Capsule: composed of poly‑D‑glutamic acid; helps the bacteria hitchhike inside macrophages and inhibits phagocytosis.

    • Protective antigen (PA): an 83‑kDa protein that forms a heptameric “prepore” on host cells, serving as a gateway for the other toxin components.

    • Edema factor (EF): an adenylate cyclase that raises intracellular cAMP, disrupting cytokine secretion and causing oedema.

    • Lethal factor (LF): a zinc‑metalloprotease that cleaves MAPK kinases, shutting down immune signalling and triggering apoptosis of immune cells.

  • Feeds on the heme of haemoglobin using secreted siderophores IsdX1 and IsdX2.

Under the microscope, Bacillus anthracis appears deceptively simple: slender rods arranged like boxcars on a railway, each bounded by a translucent sheath. This sheath is no ordinary polysaccharide; it is a cloak of poly‑D‑γ‑glutamic acid that carries a negative charge and hides the bacterium from host immune cells.

When grown on agar, colonies spread as creamy, mucus‑like ovals—a far cry from the black necrotic lesions seen in cutaneous anthrax.

Within each vegetative cell lies an oval endospore ready to withstand extremes. Only one spore forms per cell, but these dormant structures can survive in soil or animal products for decades. Spores remain inert until oxygen and nutrients coax them back to life.

Their resilience explains why anthrax outbreaks can reappear long after livestock burials or why powdered spores became a bioweapon of global concern.

What makes B. anthracis lethal is not just its endurance but its tripartite toxin. The protective antigen binds to host cells and assembles into a heptameric pore. Through this portal slip the edema factor, an enzyme that floods cells with cAMP causing swelling and immune dysregulation, and the lethal factor, a metalloprotease that slices immune signalling pathways and induces apoptosis of macrophages and dendritic cells.

These toxins, coupled with the capsule, enable the bacterium to replicate unchecked within the host.

B. anthracis is a paradox: a microbe whose stark geometry and orderly chains evoke minimalistic art, yet whose biology reflects a sophisticated armoury honed by evolution.

Its story spans ancient plagues and the foundations of microbiology, when Robert Koch used the organism to establish his germ theory and Louis Pasteur developed the first vaccines. The enduring spores have also been repurposed in modern times; their durability and ease of aerosolisation made them attractive to state bioweapons programmes.

By revealing the beauty and complexity of this pathogen, we gain a deeper appreciation for both the artistry of microbes and the vigilance needed to coexist safely with them.

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Clostridium tetani