Important role of the type VI secretion system in the virulence of an emergent human pathogen Aeromonas hydrophila: Delineating the mechanism of action of its effectors

dc.contributor.advisorAshok Chopraen_US
dc.contributor.committeeMemberVladimir Motinen_US
dc.contributor.committeeMemberVictor Reyesen_US
dc.contributor.committeeMemberVernon Teshen_US
dc.contributor.committeeMemberJohnny Petersonen_US
dc.creatorGiovanni Suarezen_US
dc.date.accessioned2011-12-20T16:05:01Z
dc.date.available2010-09-28en_US
dc.date.available2011-12-20T16:05:01Z
dc.date.created2010-07-20en_US
dc.date.issued2010-07-02en_US
dc.description.abstractAeromonas hydrophila causes various human diseases, including gastroenteritis, wound infections and septicemia. In this study, we characterized the new type 6 secretion system (T6SS) from isolate SSU of A. hydrophila and demonstrated its role in bacterial virulence. We have provided evidence that the T6SS is independent of other secretion systems and that the vasH gene is essential for the expression of the genes encoding the T6SS gene cluster. We demonstrated T6SS’s ability to translocate effector proteins into the host cells and also showed that T6SS mutants were less toxic to human and murine cell lines, and more efficiently phagocytosed by macrophages. Importantly, bacterial-host cell interaction was needed for the T6SS to induce cytotoxicity in eukaryotic cells. Based on 2-dimensional gel electrophoresis and mass spectrometric analyses of bacterial supernatants, we identified a member of the VgrG protein family, (VgrG1), containing a vegetative insecticidal protein (VIP-2) domain at its carboxyl-terminal end, as well as the hemolysin co-regulated protein (Hcp). We provided evidence that VgrG1 showed ADP-ribosyltransferase activity associated with its VIP-2 domain. Our data indicated that episomal expression of the vgrG1 gene in HeLa Tet-Off cells disrupted the actin cytoskeleton, followed by a decrease in cell viability and an increase in apoptosis. We also provided evidence that the expression of the hcp gene in HeLa cells resulted in apoptosis of the host cells without changes in their morphology. In addition, we showed that the addition of exogenous recombinant Hcp (rHcp) reduced bacterial uptake by macrophages. These results were substantiated by the in vivo analysis of cytokine profiling and activation of host immune cells after infection with the ÄvasH mutant supplemented with rHcp indicating that this T6SS effector inhibited production of pro-inflammatory cytokines and induced production of immunosuppressive cytokines, such as IL-10 and TGF-â. In summary, we showed that the T6SS represent an important virulence determinant of A. hydrophila.en_US
dc.format.mediumelectronicen_US
dc.identifier.otheretd-07202010-133212en_US
dc.identifier.urihttp://hdl.handle.net/2152.3/175
dc.language.isoengen_US
dc.rightsCopyright © is held by the author. Presentation of this material on the TDL web site by The University of Texas Medical Branch at Galveston was made possible under a limited license grant from the author who has retained all copyrights in the works.en_US
dc.subjectvirulence factorsen_US
dc.subjectvaline-glycine protein (VgrG)en_US
dc.subjecttype VI secretion systemen_US
dc.subjecthemolysin coregulated protein (Hcp)en_US
dc.subjectAeromonas hydrophilaen_US
dc.titleImportant role of the type VI secretion system in the virulence of an emergent human pathogen Aeromonas hydrophila: Delineating the mechanism of action of its effectorsen_US
dc.type.genredissertationen_US
dc.type.materialtexten_US
thesis.degree.departmentMicrobiology and Immunologyen_US
thesis.degree.grantorThe University of Texas Medical Branchen_US
thesis.degree.levelDoctoralen_US
thesis.degree.namePhDen_US

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