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Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis

The ability of bacteria to resist heat shock allows them to adapt to different environments. In addition, heat shock resistance is known for their virulence. Our previous study showed that the AI-2/luxS quorum sensing system affects the growth characteristics, biofilm formation, and virulence of Gla...

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Autores principales: Zhang, Bingzhou, Jiang, Changsheng, Cao, Hua, Zeng, Wei, Ren, Jingping, Hu, Yaofang, Li, Wentao, He, Qigai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403865/
https://www.ncbi.nlm.nih.gov/pubmed/36033895
http://dx.doi.org/10.3389/fmicb.2022.968460
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author Zhang, Bingzhou
Jiang, Changsheng
Cao, Hua
Zeng, Wei
Ren, Jingping
Hu, Yaofang
Li, Wentao
He, Qigai
author_facet Zhang, Bingzhou
Jiang, Changsheng
Cao, Hua
Zeng, Wei
Ren, Jingping
Hu, Yaofang
Li, Wentao
He, Qigai
author_sort Zhang, Bingzhou
collection PubMed
description The ability of bacteria to resist heat shock allows them to adapt to different environments. In addition, heat shock resistance is known for their virulence. Our previous study showed that the AI-2/luxS quorum sensing system affects the growth characteristics, biofilm formation, and virulence of Glaesserella parasuis. The resistance of quorum sensing system deficient G. parasuis to heat shock was obviously weaker than that of wild type strain. However, the regulatory mechanism of this phenotype remains unclear. To illustrate the regulatory mechanism by which the quorum sensing system provides resistance to heat shock, the transcriptomes of wild type (GPS2), ΔluxS, and luxS complemented (C-luxS) strains were analyzed. Four hundred forty-four differentially expressed genes were identified in quorum sensing system deficient G. parasuis, which participated in multiple regulatory pathways. Furthermore, we found that G. parasuis regulates the expression of rseA, rpoE, rseB, degS, clpP, and htrA genes to resist heat shock via the quorum sensing system. We further confirmed that rseA and rpoE genes exerted an opposite regulatory effect on heat shock resistance. In conclusion, the findings of this study provide a novel insight into how the quorum sensing system affects the transcriptome of G. parasuis and regulates its heat shock resistance property.
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spelling pubmed-94038652022-08-26 Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis Zhang, Bingzhou Jiang, Changsheng Cao, Hua Zeng, Wei Ren, Jingping Hu, Yaofang Li, Wentao He, Qigai Front Microbiol Microbiology The ability of bacteria to resist heat shock allows them to adapt to different environments. In addition, heat shock resistance is known for their virulence. Our previous study showed that the AI-2/luxS quorum sensing system affects the growth characteristics, biofilm formation, and virulence of Glaesserella parasuis. The resistance of quorum sensing system deficient G. parasuis to heat shock was obviously weaker than that of wild type strain. However, the regulatory mechanism of this phenotype remains unclear. To illustrate the regulatory mechanism by which the quorum sensing system provides resistance to heat shock, the transcriptomes of wild type (GPS2), ΔluxS, and luxS complemented (C-luxS) strains were analyzed. Four hundred forty-four differentially expressed genes were identified in quorum sensing system deficient G. parasuis, which participated in multiple regulatory pathways. Furthermore, we found that G. parasuis regulates the expression of rseA, rpoE, rseB, degS, clpP, and htrA genes to resist heat shock via the quorum sensing system. We further confirmed that rseA and rpoE genes exerted an opposite regulatory effect on heat shock resistance. In conclusion, the findings of this study provide a novel insight into how the quorum sensing system affects the transcriptome of G. parasuis and regulates its heat shock resistance property. Frontiers Media S.A. 2022-08-11 /pmc/articles/PMC9403865/ /pubmed/36033895 http://dx.doi.org/10.3389/fmicb.2022.968460 Text en Copyright © 2022 Zhang, Jiang, Cao, Zeng, Ren, Hu, Li and He. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhang, Bingzhou
Jiang, Changsheng
Cao, Hua
Zeng, Wei
Ren, Jingping
Hu, Yaofang
Li, Wentao
He, Qigai
Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis
title Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis
title_full Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis
title_fullStr Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis
title_full_unstemmed Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis
title_short Transcriptome analysis of heat resistance regulated by quorum sensing system in Glaesserella parasuis
title_sort transcriptome analysis of heat resistance regulated by quorum sensing system in glaesserella parasuis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403865/
https://www.ncbi.nlm.nih.gov/pubmed/36033895
http://dx.doi.org/10.3389/fmicb.2022.968460
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