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Regulator of RNase E activity modulates the pathogenicity of Salmonella Typhimurium

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dc.contributor.authorLee ,Jaejin-
dc.contributor.authorShin, Eunkyoung-
dc.contributor.authorYeom, Ji-Hyun-
dc.contributor.authorPark, Jaeyoung-
dc.contributor.authorKim, Sunwoo-
dc.contributor.authorLee, Minho-
dc.contributor.authorLee, Kangseok-
dc.date.accessioned2022-04-11T07:40:14Z-
dc.date.available2022-04-11T07:40:14Z-
dc.date.issued2022-04-
dc.identifier.issn0882-4010-
dc.identifier.issn1096-1208-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/56085-
dc.description.abstractRNase E-mediated RNA processing and degradation are involved in bacterial adaptation to environmental changes. The RraA regulatory protein, which is highly conserved in γ-proteobacteria, differentially modulates RNase E activity. Recent studies have revealed the association of Salmonella enterica serovar Typhimurium RNase E (STRNase E) with bacterial pathogenicity; however, the molecular mechanisms are unknown. Here, we show that the expression levels of STRraA, a protein regulator of STRNase E activity, affect S. Typhimurium pathogenicity. RNA-sequencing and RT-PCR analyses indicated positive effects of STRraA levels on the abundance of mRNA species from class II flagellar operons. Primer extension analysis further identified STRraA-regulated STRNase E cleavage in the 5′ untranslated region of fliDST mRNA. The cleavage affected the stability of this polycistronic mRNA, suggesting that STRraA protects fliDST mRNA from STRNase E cleavage, leading to enhanced flagellar assembly. Accordingly, STRraA positively regulated flagellar assembly and motility. In addition, STrraA-deleted cells showed decreased invasion ability and cytotoxicity in infection of human cervical epithelial carcinoma cells and reduced mortality in a mouse infection model compared to wild-type cells. These results support an active role of STRraA in RNase E-mediated modulation of pathogenesis in S. Typhimurium. © 2022-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titleRegulator of RNase E activity modulates the pathogenicity of Salmonella Typhimurium-
dc.typeArticle-
dc.identifier.doi10.1016/j.micpath.2022.105460-
dc.identifier.bibliographicCitationMicrobial Pathogenesis, v.165-
dc.description.isOpenAccessN-
dc.identifier.wosid000793470000005-
dc.identifier.scopusid2-s2.0-85126823504-
dc.citation.titleMicrobial Pathogenesis-
dc.citation.volume165-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordAuthorPathogenicity-
dc.subject.keywordAuthorRNase E-
dc.subject.keywordAuthorSalmonella Typhimurium-
dc.subject.keywordAuthorSTRraA-
dc.subject.keywordAuthorVirulence-
dc.subject.keywordPlusESCHERICHIA-COLI RRAA-
dc.subject.keywordPlusENTERICA SEROVAR TYPHIMURIUM-
dc.subject.keywordPlusTYPE-1 FIMBRIAL EXPRESSION-
dc.subject.keywordPlusFLAGELLAR GENE-EXPRESSION-
dc.subject.keywordPlusHOOK-ASSOCIATED PROTEINS-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusIII SECRETION-
dc.subject.keywordPlusRIBONUCLEOLYTIC ACTIVITY-
dc.subject.keywordPlusOXYGEN AVAILABILITY-
dc.subject.keywordPlusBACTERIAL FLAGELLUM-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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