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OhrR is a central transcriptional regulator of virulence in Dickeya zeae

Dickeya zeae is the causal agent of rice foot rot disease. The pathogen is known to rely on a range of virulence factors, including phytotoxin zeamines, extracellular enzymes, cell motility, and biofilm, which collectively contribute to the establishment of infections. Phytotoxin zeamines play a cri...

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Autores principales: Lv, Mingfa, Chen, Yufan, Hu, Ming, Yu, Qinglin, Duan, Cheng, Ye, Sixuan, Ling, Jinfeng, Zhou, Jianuan, Zhou, Xiaofan, Zhang, Lianhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659590/
https://www.ncbi.nlm.nih.gov/pubmed/34693617
http://dx.doi.org/10.1111/mpp.13141
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author Lv, Mingfa
Chen, Yufan
Hu, Ming
Yu, Qinglin
Duan, Cheng
Ye, Sixuan
Ling, Jinfeng
Zhou, Jianuan
Zhou, Xiaofan
Zhang, Lianhui
author_facet Lv, Mingfa
Chen, Yufan
Hu, Ming
Yu, Qinglin
Duan, Cheng
Ye, Sixuan
Ling, Jinfeng
Zhou, Jianuan
Zhou, Xiaofan
Zhang, Lianhui
author_sort Lv, Mingfa
collection PubMed
description Dickeya zeae is the causal agent of rice foot rot disease. The pathogen is known to rely on a range of virulence factors, including phytotoxin zeamines, extracellular enzymes, cell motility, and biofilm, which collectively contribute to the establishment of infections. Phytotoxin zeamines play a critical role in bacterial virulence; signalling pathways and regulatory mechanisms that govern bacterial virulence remain unclear. In this study, we identified a transcriptional regulator OhrR (organic hydroperoxide reductase regulator) that is involved in the regulation of zeamine production in D. zeae EC1. The OhrR null mutant was significantly attenuated in its virulence against rice seed, potato tubers and radish roots. Phenotype analysis showed that OhrR was also involved in the regulation of other virulence traits, including the production of extracellular cellulase, biofilm formation, and swimming/swarming motility. DNA electrophoretic mobility shift assay showed that OhrR directly regulates the transcription of key virulence genes and genes encoding bis‐(3′–5′)‐cyclic dimeric guanosine monophosphate synthetases. Furthermore, OhrR positively regulates the transcription of regulatory genes slyA and fis through binding to their promoter regions. Our findings identify a key regulator of the virulence of D. zeae and add new insights into the complex regulatory network that modulates the physiology and virulence of D. zeae.
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spelling pubmed-86595902021-12-21 OhrR is a central transcriptional regulator of virulence in Dickeya zeae Lv, Mingfa Chen, Yufan Hu, Ming Yu, Qinglin Duan, Cheng Ye, Sixuan Ling, Jinfeng Zhou, Jianuan Zhou, Xiaofan Zhang, Lianhui Mol Plant Pathol Original Articles Dickeya zeae is the causal agent of rice foot rot disease. The pathogen is known to rely on a range of virulence factors, including phytotoxin zeamines, extracellular enzymes, cell motility, and biofilm, which collectively contribute to the establishment of infections. Phytotoxin zeamines play a critical role in bacterial virulence; signalling pathways and regulatory mechanisms that govern bacterial virulence remain unclear. In this study, we identified a transcriptional regulator OhrR (organic hydroperoxide reductase regulator) that is involved in the regulation of zeamine production in D. zeae EC1. The OhrR null mutant was significantly attenuated in its virulence against rice seed, potato tubers and radish roots. Phenotype analysis showed that OhrR was also involved in the regulation of other virulence traits, including the production of extracellular cellulase, biofilm formation, and swimming/swarming motility. DNA electrophoretic mobility shift assay showed that OhrR directly regulates the transcription of key virulence genes and genes encoding bis‐(3′–5′)‐cyclic dimeric guanosine monophosphate synthetases. Furthermore, OhrR positively regulates the transcription of regulatory genes slyA and fis through binding to their promoter regions. Our findings identify a key regulator of the virulence of D. zeae and add new insights into the complex regulatory network that modulates the physiology and virulence of D. zeae. John Wiley and Sons Inc. 2021-10-24 /pmc/articles/PMC8659590/ /pubmed/34693617 http://dx.doi.org/10.1111/mpp.13141 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Lv, Mingfa
Chen, Yufan
Hu, Ming
Yu, Qinglin
Duan, Cheng
Ye, Sixuan
Ling, Jinfeng
Zhou, Jianuan
Zhou, Xiaofan
Zhang, Lianhui
OhrR is a central transcriptional regulator of virulence in Dickeya zeae
title OhrR is a central transcriptional regulator of virulence in Dickeya zeae
title_full OhrR is a central transcriptional regulator of virulence in Dickeya zeae
title_fullStr OhrR is a central transcriptional regulator of virulence in Dickeya zeae
title_full_unstemmed OhrR is a central transcriptional regulator of virulence in Dickeya zeae
title_short OhrR is a central transcriptional regulator of virulence in Dickeya zeae
title_sort ohrr is a central transcriptional regulator of virulence in dickeya zeae
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659590/
https://www.ncbi.nlm.nih.gov/pubmed/34693617
http://dx.doi.org/10.1111/mpp.13141
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