Regulation of Rab5 Function during Phagocytosis of Live Pseudomonas aeruginosa in Macrophages |
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| Authors: | Sushmita Mustafi Nathalie Rivero Joan C. Olson Philip D. Stahl M. Alejandro Barbieri |
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| Affiliation: | Department of Biological Sciences, Florida International University, Miami, Florida, USAa;Department of Microbiology, Immunology and Cell Biology, West Virginia University, Morgantown, West Virginia, USAb;Department of Cell Biology and Physiology, Washington University, School of Medicine, St. Louis, Missouri, USAc;Fairchild Tropical Botanic Garden, Coral Gables, Florida, USAd |
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| Abstract: | Pseudomonas aeruginosa, a Gram-negative opportunistic human pathogen, is a frequent cause of severe hospital-acquired infections. Effectors produced by the type III secretion system disrupt mammalian cell membrane trafficking and signaling and are integral to the establishment of P. aeruginosa infection. One of these effectors, ExoS, ADP-ribosylates several host cell proteins, including Ras and Rab GTPases. In this study, we demonstrated that Rab5 plays a critical role during early stages of P. aeruginosa invasion of J774-Eclone macrophages. We showed that live, but not heat-inactivated, P. aeruginosa inhibited phagocytosis and that this occurred in conjunction with downregulation of Rab5 activity. Inactivation of Rab5 was dependent on ExoS ADP-ribosyltransferase activity, and in J744-Eclone cells, ExoS ADP-ribosyltransferase activity caused a more severe inhibition of phagocytosis than ExoS Rho GTPase activity. Furthermore, we found that expression of Rin1, a Rab5 guanine exchange factor, but not Rabex5 and Rap6, partially reversed the inactivation of Rab5 during invasion of live P. aeruginosa. These studies provide evidence that live P. aeruginosa cells are able to influence their rate of phagocytosis in macrophages by directly regulating activation of Rab5. |
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