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OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP

Vibrio parahaemolyticus is an emerging world-wide human pathogen that is associated with food-borne gastroenteritis when raw or undercooked seafood is consumed. Expression of virulence factors in this organism is modulated by the phenomenon known as quorum sensing, which permits differential gene re...

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Autores principales: Kernell Burke, Alison, Guthrie, Leah T. C., Modise, Thero, Cormier, Guy, Jensen, Roderick V., McCarter, Linda L., Stevens, Ann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406679/
https://www.ncbi.nlm.nih.gov/pubmed/25901572
http://dx.doi.org/10.1371/journal.pone.0121863
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author Kernell Burke, Alison
Guthrie, Leah T. C.
Modise, Thero
Cormier, Guy
Jensen, Roderick V.
McCarter, Linda L.
Stevens, Ann M.
author_facet Kernell Burke, Alison
Guthrie, Leah T. C.
Modise, Thero
Cormier, Guy
Jensen, Roderick V.
McCarter, Linda L.
Stevens, Ann M.
author_sort Kernell Burke, Alison
collection PubMed
description Vibrio parahaemolyticus is an emerging world-wide human pathogen that is associated with food-borne gastroenteritis when raw or undercooked seafood is consumed. Expression of virulence factors in this organism is modulated by the phenomenon known as quorum sensing, which permits differential gene regulation at low versus high cell density. The master regulator of quorum sensing in V. parahaemolyticus is OpaR. OpaR not only controls virulence factor gene expression, but also the colony and cellular morphology associated with growth on a surface and biofilm formation. Whole transcriptome Next Generation sequencing (RNA-Seq) was utilized to determine the OpaR regulon by comparing strains BB22OP (opaR (+), LM5312) and BB22TR (∆opaR1, LM5674). This work, using the published V. parahaemolyticus BB22OP genome sequence, confirms and expands upon a previous microarray analysis for these two strains that used an Affymetrix GeneChip designed from the closely related V. parahaemolyticus RIMD2210633 genome sequence. Overall there was excellent correlation between the microarray and RNA-Seq data. Eleven transcription factors under OpaR control were identified by both methods and further confirmed by quantitative reverse transcription PCR (qRT-PCR) analysis. Nine of these transcription factors were demonstrated to be direct OpaR targets via in vitro electrophoretic mobility shift assays with purified hexahistidine-tagged OpaR. Identification of the direct and indirect targets of OpaR, including small RNAs, will enable the construction of a network map of regulatory interactions important for the switch between the nonpathogenic and pathogenic states.
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spelling pubmed-44066792015-05-07 OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP Kernell Burke, Alison Guthrie, Leah T. C. Modise, Thero Cormier, Guy Jensen, Roderick V. McCarter, Linda L. Stevens, Ann M. PLoS One Research Article Vibrio parahaemolyticus is an emerging world-wide human pathogen that is associated with food-borne gastroenteritis when raw or undercooked seafood is consumed. Expression of virulence factors in this organism is modulated by the phenomenon known as quorum sensing, which permits differential gene regulation at low versus high cell density. The master regulator of quorum sensing in V. parahaemolyticus is OpaR. OpaR not only controls virulence factor gene expression, but also the colony and cellular morphology associated with growth on a surface and biofilm formation. Whole transcriptome Next Generation sequencing (RNA-Seq) was utilized to determine the OpaR regulon by comparing strains BB22OP (opaR (+), LM5312) and BB22TR (∆opaR1, LM5674). This work, using the published V. parahaemolyticus BB22OP genome sequence, confirms and expands upon a previous microarray analysis for these two strains that used an Affymetrix GeneChip designed from the closely related V. parahaemolyticus RIMD2210633 genome sequence. Overall there was excellent correlation between the microarray and RNA-Seq data. Eleven transcription factors under OpaR control were identified by both methods and further confirmed by quantitative reverse transcription PCR (qRT-PCR) analysis. Nine of these transcription factors were demonstrated to be direct OpaR targets via in vitro electrophoretic mobility shift assays with purified hexahistidine-tagged OpaR. Identification of the direct and indirect targets of OpaR, including small RNAs, will enable the construction of a network map of regulatory interactions important for the switch between the nonpathogenic and pathogenic states. Public Library of Science 2015-04-22 /pmc/articles/PMC4406679/ /pubmed/25901572 http://dx.doi.org/10.1371/journal.pone.0121863 Text en © 2015 Kernell Burke et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kernell Burke, Alison
Guthrie, Leah T. C.
Modise, Thero
Cormier, Guy
Jensen, Roderick V.
McCarter, Linda L.
Stevens, Ann M.
OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP
title OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP
title_full OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP
title_fullStr OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP
title_full_unstemmed OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP
title_short OpaR Controls a Network of Downstream Transcription Factors in Vibrio parahaemolyticus BB22OP
title_sort opar controls a network of downstream transcription factors in vibrio parahaemolyticus bb22op
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406679/
https://www.ncbi.nlm.nih.gov/pubmed/25901572
http://dx.doi.org/10.1371/journal.pone.0121863
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