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Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA
RovA is known to enhance Yersinia pestis virulence by directly upregulating the psa loci. This work presents a complex gene regulatory paradigm involving the reciprocal regulatory action of RovM and RovA on the expression of biofilm and virulence genes as well as on their own genes. RovM and RovA en...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821237/ https://www.ncbi.nlm.nih.gov/pubmed/26984293 http://dx.doi.org/10.1098/rsob.150198 |
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author | Liu, Lei Fang, Haihong Yang, Huiying Zhang, Yiquan Han, Yanping Zhou, Dongsheng Yang, Ruifu |
author_facet | Liu, Lei Fang, Haihong Yang, Huiying Zhang, Yiquan Han, Yanping Zhou, Dongsheng Yang, Ruifu |
author_sort | Liu, Lei |
collection | PubMed |
description | RovA is known to enhance Yersinia pestis virulence by directly upregulating the psa loci. This work presents a complex gene regulatory paradigm involving the reciprocal regulatory action of RovM and RovA on the expression of biofilm and virulence genes as well as on their own genes. RovM and RovA enhance and inhibit Y. pestis biofilm production, respectively, whereas RovM represses virulence in mice. RovM directly stimulates the transcription of hmsT, hmsCDE and rovM, while indirectly enhancing hmsHFRS transcription. It also indirectly represses hmsP transcription. By contrast, RovA directly represses hmsT transcription and indirectly inhibits waaAE-coaD transcription, while RovM inhibits psaABC and psaEF transcription by directly repressing rovA transcription. rovM expression is significantly upregulated at 26°C (the temperature of the flea gut) relative to 37°C (the warm-blooded host temperature). We speculate that upregulation of rovM together with downregulation of rovA in the flea gut would promote Y. pestis biofilm formation while inhibiting virulence gene expression, leading to a more transmissible infection of this pathogen in fleas. Once the bacterium shifts to a lifestyle in the warm-blooded hosts, inhibited RovM production accompanied by recovered RovA synthesis would encourage virulence factor production and inhibit biofilm gene expression. |
format | Online Article Text |
id | pubmed-4821237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48212372016-04-11 Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA Liu, Lei Fang, Haihong Yang, Huiying Zhang, Yiquan Han, Yanping Zhou, Dongsheng Yang, Ruifu Open Biol Research RovA is known to enhance Yersinia pestis virulence by directly upregulating the psa loci. This work presents a complex gene regulatory paradigm involving the reciprocal regulatory action of RovM and RovA on the expression of biofilm and virulence genes as well as on their own genes. RovM and RovA enhance and inhibit Y. pestis biofilm production, respectively, whereas RovM represses virulence in mice. RovM directly stimulates the transcription of hmsT, hmsCDE and rovM, while indirectly enhancing hmsHFRS transcription. It also indirectly represses hmsP transcription. By contrast, RovA directly represses hmsT transcription and indirectly inhibits waaAE-coaD transcription, while RovM inhibits psaABC and psaEF transcription by directly repressing rovA transcription. rovM expression is significantly upregulated at 26°C (the temperature of the flea gut) relative to 37°C (the warm-blooded host temperature). We speculate that upregulation of rovM together with downregulation of rovA in the flea gut would promote Y. pestis biofilm formation while inhibiting virulence gene expression, leading to a more transmissible infection of this pathogen in fleas. Once the bacterium shifts to a lifestyle in the warm-blooded hosts, inhibited RovM production accompanied by recovered RovA synthesis would encourage virulence factor production and inhibit biofilm gene expression. The Royal Society 2016-03-16 /pmc/articles/PMC4821237/ /pubmed/26984293 http://dx.doi.org/10.1098/rsob.150198 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Liu, Lei Fang, Haihong Yang, Huiying Zhang, Yiquan Han, Yanping Zhou, Dongsheng Yang, Ruifu Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA |
title | Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA |
title_full | Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA |
title_fullStr | Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA |
title_full_unstemmed | Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA |
title_short | Reciprocal regulation of Yersinia pestis biofilm formation and virulence by RovM and RovA |
title_sort | reciprocal regulation of yersinia pestis biofilm formation and virulence by rovm and rova |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821237/ https://www.ncbi.nlm.nih.gov/pubmed/26984293 http://dx.doi.org/10.1098/rsob.150198 |
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