Pseudomonas aeruginosa induces type-III-secretion-mediated apoptosis of macrophages and epithelial cells
1Departments of Medicine, University of California, San Francisco, San Francisco, California 94143, USA.
Abstract:
Pseudomonas aeruginosa is a gram-negative opportunistic pathogen that is cytotoxic towards a variety of eukaryotic cells. To investigate the effect of this bacterium on macrophages, we infected J774A.1 cells and primary bone-marrow-derived murine macrophages with the P. aeruginosa strain PA103 in vitro. PA103 caused type-III-secretion-dependent killing of macrophages within 2 h of infection. Only a portion of the killing required the putative cytotoxin ExoU. By three criteria, terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling assays, cytoplasmic nucleosome assays, and Hoechst staining, the ExoU-independent but type-III-secretion-dependent killing exhibited features of apoptosis. Extracellular bacteria were capable of inducing apoptosis, and some laboratory and clinical isolates of P. aeruginosa induced significantly higher levels of this form of cell death than others. Interestingly, HeLa cells but not Madin-Darby canine kidney cells were susceptible to type-III-secretion-mediated apoptosis under the conditions of these assays. These findings are consistent with a model in which the P. aeruginosa type III secretion system transports at least two factors that kill macrophages: ExoU, which causes necrosis, and a second, as yet unidentified, effector protein, which induces apoptosis. Such killing may contribute to the ability of this organism to persist and disseminate within infected patients.
Insights
Pseudomonas aeruginosa kills macrophages through type-III secretion. This process involves ExoU-dependent necrosis and ExoU-independent apoptosis, contributing to bacterial persistence.
Area of Science:
- Microbiology
- Cell Biology
- Pathogenesis
Background:
- Pseudomonas aeruginosa is a gram-negative opportunistic pathogen.
- It exhibits cytotoxicity towards various eukaryotic cells, including macrophages.
Purpose of the Study:
- To investigate the effects of P. aeruginosa on macrophages.
- To elucidate the mechanisms of macrophage killing by P. aeruginosa.
Main Methods:
- In vitro infection of J774A.1 cells and primary murine macrophages with P. aeruginosa strain PA103.
- Assays used to detect apoptosis: terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL), cytoplasmic nucleosome assays, and Hoechst staining.
Main Results:
- PA103 induced type-III-secretion-dependent macrophage killing within 2 hours.
- Macrophage killing involved both ExoU-dependent necrosis and ExoU-independent apoptosis.
- Extracellular bacteria induced apoptosis, with varying levels observed among different P. aeruginosa isolates.
- HeLa cells were susceptible to type-III secretion-mediated apoptosis, but Madin-Darby canine kidney cells were not.
Conclusions:
- P. aeruginosa utilizes its type III secretion system to deliver at least two factors to kill macrophages.
- ExoU causes necrosis, while a second, unidentified effector induces apoptosis.
- This dual killing mechanism may facilitate P. aeruginosa persistence and dissemination in infected patients.
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