OxyR positively and directly regulates vi polysaccharide capsular antigen in Salmonella enterica serovar Typhi

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dc.contributor.author Zhang, Y.
dc.contributor.author Chong, X.
dc.contributor.author Xia, L.
dc.contributor.author Lu, R.
dc.contributor.author Osei-Adjei, G.
dc.contributor.author Zhang, Y.
dc.contributor.author Huang, X.
dc.date.accessioned 2022-09-08T09:36:32Z
dc.date.available 2022-09-08T09:36:32Z
dc.date.issued 2018
dc.identifier.other 10.1016/j.micpath.2018.08.050
dc.identifier.uri https://pubmed.ncbi.nlm.nih.gov/30145252/
dc.identifier.uri http://atuspace.atu.edu.gh:8080/handle/123456789/211
dc.description.abstract Salmonella enterica serovar Typhi (S. Typhi) is a human enteropathogen that can overcome oxidative stress and survive in macrophages. OxyR is an important part of the antioxidant defense system. S. Typhi expresses a virulence (Vi) polysaccharide capsular antigen, which provides the bacterium with the ability to avoid host defenses and suppress detection by the innate immune system. This study investigated the effect of OxyR on Vi antigen in S. Typhi. In the oxyR mutant strain, microarray analysis, quantitative real time PCR and β-galactosidase assay confirmed that the viaB operon was positively regulated by OxyR. The Vi enzyme-linked immunosorbent assay and flow cytometry results showed that Vi capsule level was decreased in the oxyR mutant strain. Also, the EMSA revealed that OxyR directly binds to the promoter region of tviA. Thus, we propose that S. Typhi OxyR positively regulates expression of Vi capsule antigen in a direct manner. en_US
dc.language.iso en en_US
dc.publisher Elsevier Ltd en_US
dc.relation.ispartofseries vol;124
dc.subject OxyR en_US
dc.subject Salmonella enterica serovar Typhi en_US
dc.subject Vi polysaccharide capsular antigen en_US
dc.title OxyR positively and directly regulates vi polysaccharide capsular antigen in Salmonella enterica serovar Typhi en_US
dc.type Article en_US


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