Early Bacillus anthracis-macrophage interactions: intracellular survival survival and escape

T C Dixon1, A A Fadl, T M Koehler

  • 1Department of Microbiology, Duke University Medical Center, Durham, NC 27710, USA.

Cellular Microbiology
|February 24, 2001
PubMed

Insights

Bacillus anthracis endospores germinate inside macrophages, escaping to replicate within the cytoplasm. Toxin plasmid pXO1, specifically the atxA transactivator, is essential for this bacterial release from host cells.

Area of Science:

  • Microbiology
  • Pathogenesis
  • Cell Biology

Background:

  • Bacillus anthracis infections begin with endospore entry and macrophage engulfment.
  • Systemic anthrax involves high bacterial loads and exotoxin production, leading to severe disease.
  • Early intracellular events are critical for understanding anthrax establishment.

Purpose of the Study:

  • To investigate the early intracellular events of Bacillus anthracis infection.
  • To determine the mechanisms of bacterial escape from macrophages.
  • To identify genetic factors influencing bacterial release from host cells.

Main Methods:

  • Culturing of macrophages and infection with Bacillus anthracis endospores.
  • Microscopic observation of intracellular bacterial behavior.
  • Genetic analysis using mutant strains and plasmid-deficient bacteria.

Main Results:

  • Vegetative Bacillus anthracis cells escape phagocytic vesicles and replicate within macrophage cytoplasm.
  • Bacterial release from macrophages occurs 4-6 hours post-phagocytosis.
  • The toxin plasmid pXO1, particularly the atxA transactivator, is required for release, while pXO2 is not.

Conclusions:

  • Macrophage release of Bacillus anthracis is regulated by the atxA transactivator on pXO1.
  • The toxin genes themselves are not necessary for bacterial escape from macrophages.
  • Putative 'escape' genes may reside on the chromosome or pXO1 plasmid.

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