| Literature DB >> 26930702 |
Ayan Mondal1, Rima Tapader1, Nabendu Sekhar Chatterjee2, Amit Ghosh1, Ritam Sinha3, Hemanta Koley3, Dhira Rani Saha4, Manoj K Chakrabarti1, Sun Nyunt Wai5, Amit Pal6.
Abstract
Proteases in Vibrio cholerae have been shown to play a role in its pathogenesis. V. cholerae secretes Zn-dependent hemagglutinin protease (HAP) and calcium-dependent trypsin-like serine protease (VesC) by using the type II secretion system (TIISS). Our present studies demonstrated that these proteases are also secreted in association with outer membrane vesicles (OMVs) and transported to human intestinal epithelial cells in an active form. OMV-associated HAP induces dose-dependent apoptosis in Int407 cells and an enterotoxic response in the mouse ileal loop (MIL) assay, whereas OMV-associated VesC showed a hemorrhagic fluid response in the MIL assay, necrosis in Int407 cells, and an increased interleukin-8 (IL-8) response in T84 cells, which were significantly reduced in OMVs from VesC mutant strain. Our results also showed that serine protease VesC plays a role in intestinal colonization of V. cholerae strains in adult mice. In conclusion, our study shows that V. cholerae OMVs secrete biologically active proteases which may play a role in cytotoxic and inflammatory responses.Entities:
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Year: 2016 PMID: 26930702 PMCID: PMC4862697 DOI: 10.1128/IAI.01365-15
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441