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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.
Abstract:
This study describes early intracellular events occurring during the establishment phase of Bacillus anthracis infections. Anthrax infections are initiated by dormant endospores gaining access to the mammalian host and becoming engulfed by regional macrophages (Mphi). During systemic anthrax, late stage events include vegetative growth in the blood to very high titres and the synthesis of the anthrax exotoxin complex, which causes disease symptoms and death. Experiments focus on the early events occurring during the first few hours of the B. anthracis infectious cycle, from endospore germination up to and including release of the vegetative cell from phagocytes. We found that newly vegetative bacilli escape from the phagocytic vesicles of cultured Mphi and replicate within the cytoplasm of these cells. Release from the Mphi occurs 4-6 h after endospore phagocytosis, timing that correlates with anthrax infection of test animals. Genetic analysis from this study indicates that the toxin plasmid pXO1 is required for release from the Mphi, whereas the capsule plasmid pXO2 is not. The transactivator atxA, located on pXO1, is also found to be essential for release, but the toxin genes themselves are not required. This suggests that Mphi release of anthrax bacilli is atxA regulated. The putative 'escape' genes may be located on the chromosome and/or on pXO1.
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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