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PLoS One. 2011 Mar 31;6(3):e18367. doi: 10.1371/journal.pone.0018367.

Mycobacterium tuberculosis induces an atypical cell death mode to escape from infected macrophages.

Author information

1
Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.

Abstract

BACKGROUND:

Macrophage cell death following infection with Mycobacterium tuberculosis plays a central role in tuberculosis disease pathogenesis. Certain attenuated strains induce extrinsic apoptosis of infected macrophages but virulent strains of M. tuberculosis suppress this host response. We previously reported that virulent M. tuberculosis induces cell death when bacillary load exceeds ∼20 per macrophage but the precise nature of this demise has not been defined.

METHODOLOGY/PRINCIPAL FINDINGS:

We analyzed the characteristics of cell death in primary murine macrophages challenged with virulent or attenuated M. tuberculosis complex strains. We report that high intracellular bacillary burden causes rapid and primarily necrotic death via lysosomal permeabilization, releasing hydrolases that promote Bax/Bak-independent mitochondrial damage and necrosis. Cell death was independent of cathepsins B or L and notable for ultrastructural evidence of damage to lipid bilayers throughout host cells with depletion of several host phospholipid species. These events require viable bacteria that can respond to intracellular cues via the PhoPR sensor kinase system but are independent of the ESX1 system.

CONCLUSIONS/SIGNIFICANCE:

Cell death caused by virulent M. tuberculosis is distinct from classical apoptosis, pyroptosis or pyronecrosis. Mycobacterial genes essential for cytotoxicity are regulated by the PhoPR two-component system. This atypical death mode provides a mechanism for viable bacilli to exit host macrophages for spreading infection and the eventual transition to extracellular persistence that characterizes advanced pulmonary tuberculosis.

PMID:
21483832
PMCID:
PMC3069075
DOI:
10.1371/journal.pone.0018367
[Indexed for MEDLINE]
Free PMC Article
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