Xue Li, Wei Lian, Miaomiao Zhang, Xi Luo, Yiquan Zhang, Renfei Lu
{"title":"QsvR and OpaR coordinately regulate the transcription of <i>cpsS</i> and <i>cpsR</i> in <i>Vibrio parahaemolyticus</i>.","authors":"Xue Li, Wei Lian, Miaomiao Zhang, Xi Luo, Yiquan Zhang, Renfei Lu","doi":"10.1139/cjm-2023-0196","DOIUrl":null,"url":null,"abstract":"<p><p><i>Vibrio parahaemolyticus</i>, the leading cause of seafood-associated gastroenteritis, has a strong capacity to form biofilms on surfaces, which is strictly regulated by the CpsS-CpsR-CpsQ regulatory cascade. OpaR, a master regulator of quorum sensing, is a global regulator that controls multiple cellular pathways including biofilm formation and virulence. QsvR is an AraC-type regulator that works coordinately with OpaR to control biofilm formation and virulence gene expression of <i>V. parahaemolyticus</i>. QsvR and OpaR activate <i>cpsQ</i> transcription. OpaR also activates <i>cpsR</i> transcription, but lacks the detailed regulatory mechanisms. Furthermore, it is still unknown whether QsvR regulates <i>cpsR</i> transcription, as well as whether QsvR and OpaR regulate <i>cpsS</i> transcription. In this study, the results of quantitative real-time PCR and LacZ fusion assays demonstrated that deletion of <i>qsvR</i> and/or <i>opaR</i> significantly decreased the expression levels of <i>cpsS</i> and <i>cpsR</i> compared to the wild-type strain. However, the results of two-plasmid <i>lacZ</i> reporter and electrophoretic mobility-shift assays showed that both QsvR and OpaR were unable to bind the regulatory DNA regions of <i>cpsS</i> and <i>cpsR</i>. Therefore, transcription of <i>cpsS</i> and <i>cpsR</i> was coordinately and indirectly activated by QsvR and OpaR. This work enriched our knowledge on the regulatory network of biofilm formation in <i>V. parahaemolyticus</i>.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"128-134"},"PeriodicalIF":1.8000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian journal of microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1139/cjm-2023-0196","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/28 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Vibrio parahaemolyticus, the leading cause of seafood-associated gastroenteritis, has a strong capacity to form biofilms on surfaces, which is strictly regulated by the CpsS-CpsR-CpsQ regulatory cascade. OpaR, a master regulator of quorum sensing, is a global regulator that controls multiple cellular pathways including biofilm formation and virulence. QsvR is an AraC-type regulator that works coordinately with OpaR to control biofilm formation and virulence gene expression of V. parahaemolyticus. QsvR and OpaR activate cpsQ transcription. OpaR also activates cpsR transcription, but lacks the detailed regulatory mechanisms. Furthermore, it is still unknown whether QsvR regulates cpsR transcription, as well as whether QsvR and OpaR regulate cpsS transcription. In this study, the results of quantitative real-time PCR and LacZ fusion assays demonstrated that deletion of qsvR and/or opaR significantly decreased the expression levels of cpsS and cpsR compared to the wild-type strain. However, the results of two-plasmid lacZ reporter and electrophoretic mobility-shift assays showed that both QsvR and OpaR were unable to bind the regulatory DNA regions of cpsS and cpsR. Therefore, transcription of cpsS and cpsR was coordinately and indirectly activated by QsvR and OpaR. This work enriched our knowledge on the regulatory network of biofilm formation in V. parahaemolyticus.
期刊介绍:
Published since 1954, the Canadian Journal of Microbiology is a monthly journal that contains new research in the field of microbiology, including applied microbiology and biotechnology; microbial structure and function; fungi and other eucaryotic protists; infection and immunity; microbial ecology; physiology, metabolism and enzymology; and virology, genetics, and molecular biology. It also publishes review articles and notes on an occasional basis, contributed by recognized scientists worldwide.