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Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure

Arsenic (As) resistance determinant ars operon is present in many bacteria and has been demonstrated to enhance As(V) resistance of bacteria. However, whole molecular mechanism adaptations of bacteria in response to As(V) stress remain largely unknown. In this study, transcriptional profiles of Ente...

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Autores principales: Zhang, Yingjiao, Chen, Songcan, Hao, Xiuli, Su, Jian-Qiang, Xue, Ximei, Yan, Yu, Zhu, Yong-Guan, Ye, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852401/
https://www.ncbi.nlm.nih.gov/pubmed/27199962
http://dx.doi.org/10.3389/fmicb.2016.00636
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author Zhang, Yingjiao
Chen, Songcan
Hao, Xiuli
Su, Jian-Qiang
Xue, Ximei
Yan, Yu
Zhu, Yong-Guan
Ye, Jun
author_facet Zhang, Yingjiao
Chen, Songcan
Hao, Xiuli
Su, Jian-Qiang
Xue, Ximei
Yan, Yu
Zhu, Yong-Guan
Ye, Jun
author_sort Zhang, Yingjiao
collection PubMed
description Arsenic (As) resistance determinant ars operon is present in many bacteria and has been demonstrated to enhance As(V) resistance of bacteria. However, whole molecular mechanism adaptations of bacteria in response to As(V) stress remain largely unknown. In this study, transcriptional profiles of Enterobacteriaceae strain LSJC7 responding to As(V) stress were analyzed using RNA-seq and qRT-PCR. As expected, genes involved in As(V) uptake were down-regulated, those involved in As(V) reduction and As(III) efflux were up-regulated, which avoided cellular As accumulation. Reactive oxygen species and nitric oxide (NO) were induced, which caused cellular damages including DNA, protein, and Fe–S cluster damage in LSJC7. The expression of specific genes encoding transcriptional regulators, such as nsrR and soxRS were also induced. NsrR and SoxRS modulated many critical metabolic activities in As(V) stressed LSJC7 cells, including reactive species scavenging and repairing damaged DNA, proteins, and Fe–S clusters. Therefore, besides As uptake, reduction, and efflux; oxidative stress defense and damage repair were the main cellular adaptive responses of LSJC7 to As(V) stress.
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spelling pubmed-48524012016-05-19 Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure Zhang, Yingjiao Chen, Songcan Hao, Xiuli Su, Jian-Qiang Xue, Ximei Yan, Yu Zhu, Yong-Guan Ye, Jun Front Microbiol Microbiology Arsenic (As) resistance determinant ars operon is present in many bacteria and has been demonstrated to enhance As(V) resistance of bacteria. However, whole molecular mechanism adaptations of bacteria in response to As(V) stress remain largely unknown. In this study, transcriptional profiles of Enterobacteriaceae strain LSJC7 responding to As(V) stress were analyzed using RNA-seq and qRT-PCR. As expected, genes involved in As(V) uptake were down-regulated, those involved in As(V) reduction and As(III) efflux were up-regulated, which avoided cellular As accumulation. Reactive oxygen species and nitric oxide (NO) were induced, which caused cellular damages including DNA, protein, and Fe–S cluster damage in LSJC7. The expression of specific genes encoding transcriptional regulators, such as nsrR and soxRS were also induced. NsrR and SoxRS modulated many critical metabolic activities in As(V) stressed LSJC7 cells, including reactive species scavenging and repairing damaged DNA, proteins, and Fe–S clusters. Therefore, besides As uptake, reduction, and efflux; oxidative stress defense and damage repair were the main cellular adaptive responses of LSJC7 to As(V) stress. Frontiers Media S.A. 2016-05-02 /pmc/articles/PMC4852401/ /pubmed/27199962 http://dx.doi.org/10.3389/fmicb.2016.00636 Text en Copyright © 2016 Zhang, Chen, Hao, Su, Xue, Yan, Zhu and Ye. http://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) or licensor 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, Yingjiao
Chen, Songcan
Hao, Xiuli
Su, Jian-Qiang
Xue, Ximei
Yan, Yu
Zhu, Yong-Guan
Ye, Jun
Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure
title Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure
title_full Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure
title_fullStr Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure
title_full_unstemmed Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure
title_short Transcriptomic Analysis Reveals Adaptive Responses of an Enterobacteriaceae Strain LSJC7 to Arsenic Exposure
title_sort transcriptomic analysis reveals adaptive responses of an enterobacteriaceae strain lsjc7 to arsenic exposure
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852401/
https://www.ncbi.nlm.nih.gov/pubmed/27199962
http://dx.doi.org/10.3389/fmicb.2016.00636
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