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Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae
Bacteria use quorum sensing to monitor cell density and coordinate group behaviours. In Vibrio cholerae, the causative agent of the diarrheal disease cholera, quorum sensing is connected to virulence gene expression via the two autoinducer molecules, AI-2 and CAI-1. Both autoinducers share one signa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451090/ https://www.ncbi.nlm.nih.gov/pubmed/30649554 http://dx.doi.org/10.1093/nar/gky1320 |
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author | Herzog, Roman Peschek, Nikolai Fröhlich, Kathrin S Schumacher, Kilian Papenfort, Kai |
author_facet | Herzog, Roman Peschek, Nikolai Fröhlich, Kathrin S Schumacher, Kilian Papenfort, Kai |
author_sort | Herzog, Roman |
collection | PubMed |
description | Bacteria use quorum sensing to monitor cell density and coordinate group behaviours. In Vibrio cholerae, the causative agent of the diarrheal disease cholera, quorum sensing is connected to virulence gene expression via the two autoinducer molecules, AI-2 and CAI-1. Both autoinducers share one signal transduction pathway to control the production of AphA, a key transcriptional activator of biofilm formation and virulence genes. In this study, we demonstrate that the recently identified autoinducer, DPO, also controls AphA production in V. cholerae. DPO, functioning through the transcription factor VqmA and the VqmR small RNA, reduces AphA levels at the post-transcriptional level and consequently inhibits virulence gene expression. VqmR-mediated repression of AphA provides an important link between the AI-2/CAI-1 and DPO-dependent quorum sensing pathways in V. cholerae. Transcriptome analyses comparing the effect of single autoinducers versus autoinducer combinations show that quorum sensing controls the expression of ∼400 genes in V. cholerae and that all three autoinducers are required for a full quorum sensing response. Together, our data provide a global view on autoinducer interplay in V. cholerae and highlight the importance of RNA-based gene control for collective functions in this major human pathogen. |
format | Online Article Text |
id | pubmed-6451090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64510902019-04-09 Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae Herzog, Roman Peschek, Nikolai Fröhlich, Kathrin S Schumacher, Kilian Papenfort, Kai Nucleic Acids Res RNA and RNA-protein complexes Bacteria use quorum sensing to monitor cell density and coordinate group behaviours. In Vibrio cholerae, the causative agent of the diarrheal disease cholera, quorum sensing is connected to virulence gene expression via the two autoinducer molecules, AI-2 and CAI-1. Both autoinducers share one signal transduction pathway to control the production of AphA, a key transcriptional activator of biofilm formation and virulence genes. In this study, we demonstrate that the recently identified autoinducer, DPO, also controls AphA production in V. cholerae. DPO, functioning through the transcription factor VqmA and the VqmR small RNA, reduces AphA levels at the post-transcriptional level and consequently inhibits virulence gene expression. VqmR-mediated repression of AphA provides an important link between the AI-2/CAI-1 and DPO-dependent quorum sensing pathways in V. cholerae. Transcriptome analyses comparing the effect of single autoinducers versus autoinducer combinations show that quorum sensing controls the expression of ∼400 genes in V. cholerae and that all three autoinducers are required for a full quorum sensing response. Together, our data provide a global view on autoinducer interplay in V. cholerae and highlight the importance of RNA-based gene control for collective functions in this major human pathogen. Oxford University Press 2019-04-08 2019-01-15 /pmc/articles/PMC6451090/ /pubmed/30649554 http://dx.doi.org/10.1093/nar/gky1320 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA and RNA-protein complexes Herzog, Roman Peschek, Nikolai Fröhlich, Kathrin S Schumacher, Kilian Papenfort, Kai Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae |
title | Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae |
title_full | Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae |
title_fullStr | Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae |
title_full_unstemmed | Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae |
title_short | Three autoinducer molecules act in concert to control virulence gene expression in Vibrio cholerae |
title_sort | three autoinducer molecules act in concert to control virulence gene expression in vibrio cholerae |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451090/ https://www.ncbi.nlm.nih.gov/pubmed/30649554 http://dx.doi.org/10.1093/nar/gky1320 |
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