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Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni

Campylobacter jejuni is an important foodborne pathogen. The molecular mechanisms for the regulation of oxidative stress resistance have not yet been understood fully in this bacterium. In this study, we investigated how PerR (peroxide stress regulator) modulates the transcriptional regulation of bo...

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Autores principales: Kim, Jong-Chul, Oh, Euna, Hwang, Sunyoung, Ryu, Sangryeol, Jeon, Byeonghwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330884/
https://www.ncbi.nlm.nih.gov/pubmed/25741333
http://dx.doi.org/10.3389/fmicb.2015.00126
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author Kim, Jong-Chul
Oh, Euna
Hwang, Sunyoung
Ryu, Sangryeol
Jeon, Byeonghwa
author_facet Kim, Jong-Chul
Oh, Euna
Hwang, Sunyoung
Ryu, Sangryeol
Jeon, Byeonghwa
author_sort Kim, Jong-Chul
collection PubMed
description Campylobacter jejuni is an important foodborne pathogen. The molecular mechanisms for the regulation of oxidative stress resistance have not yet been understood fully in this bacterium. In this study, we investigated how PerR (peroxide stress regulator) modulates the transcriptional regulation of both peroxide and superoxide resistance genes in C. jejuni, particularly under oxidative stress conditions. The transcriptional levels of ahpC, katA, and sodB were substantially increased by aeration and oxidant exposure. Interestingly, a perR mutation completely abrogated the transcriptional response of ahpC, katA and sodB to oxidants. Furthermore, we demonstrated that perR transcription was reduced by aeration and oxidant exposure. In contrast to the unique role of PerR homologs in peroxide stress regulation in other bacteria, C. jejuni PerR directly regulates the transcription of sodB, the most important gene in superoxide defense, as evidenced by the alteration of sodB transcription by the perR mutation and direct binding of rPerR to the sodB promoter. In addition, we also observed notable morphological changes in C. jejuni from spiral rods to cocoid morphology under aerobic conditions. Based on the intracellular ATP levels, C. jejuni entered a viable-but-non-culturable (VBNC) state under aerobic conditions. These findings clearly demonstrate that C. jejuni possesses a unique regulatory mechanism of oxidative stress defense that does not specifically distinguish between peroxide and superoxide defense, and PerR plays a pivotal role in this non-selective regulation of oxidative stress resistance in C. jejuni.
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spelling pubmed-43308842015-03-04 Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni Kim, Jong-Chul Oh, Euna Hwang, Sunyoung Ryu, Sangryeol Jeon, Byeonghwa Front Microbiol Microbiology Campylobacter jejuni is an important foodborne pathogen. The molecular mechanisms for the regulation of oxidative stress resistance have not yet been understood fully in this bacterium. In this study, we investigated how PerR (peroxide stress regulator) modulates the transcriptional regulation of both peroxide and superoxide resistance genes in C. jejuni, particularly under oxidative stress conditions. The transcriptional levels of ahpC, katA, and sodB were substantially increased by aeration and oxidant exposure. Interestingly, a perR mutation completely abrogated the transcriptional response of ahpC, katA and sodB to oxidants. Furthermore, we demonstrated that perR transcription was reduced by aeration and oxidant exposure. In contrast to the unique role of PerR homologs in peroxide stress regulation in other bacteria, C. jejuni PerR directly regulates the transcription of sodB, the most important gene in superoxide defense, as evidenced by the alteration of sodB transcription by the perR mutation and direct binding of rPerR to the sodB promoter. In addition, we also observed notable morphological changes in C. jejuni from spiral rods to cocoid morphology under aerobic conditions. Based on the intracellular ATP levels, C. jejuni entered a viable-but-non-culturable (VBNC) state under aerobic conditions. These findings clearly demonstrate that C. jejuni possesses a unique regulatory mechanism of oxidative stress defense that does not specifically distinguish between peroxide and superoxide defense, and PerR plays a pivotal role in this non-selective regulation of oxidative stress resistance in C. jejuni. Frontiers Media S.A. 2015-02-17 /pmc/articles/PMC4330884/ /pubmed/25741333 http://dx.doi.org/10.3389/fmicb.2015.00126 Text en Copyright © 2015 Kim, Oh, Hwang, Ryu and Jeon. 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
Kim, Jong-Chul
Oh, Euna
Hwang, Sunyoung
Ryu, Sangryeol
Jeon, Byeonghwa
Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni
title Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni
title_full Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni
title_fullStr Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni
title_full_unstemmed Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni
title_short Non-selective regulation of peroxide and superoxide resistance genes by PerR in Campylobacter jejuni
title_sort non-selective regulation of peroxide and superoxide resistance genes by perr in campylobacter jejuni
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330884/
https://www.ncbi.nlm.nih.gov/pubmed/25741333
http://dx.doi.org/10.3389/fmicb.2015.00126
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