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The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress

Bacteria can withstand various types of environmental osmostress. A sudden rise in osmostress affects bacterial cell growth that is countered by activating special genes. The change of osmostress is generally a slow process under the natural environment. However, the collective response of bacteria...

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Autores principales: Li, Kaihuai, Liao, Jinxing, Wei, Ming, Qiu, Shanxu, Wu, Weiyin, Zhao, Yancun, Wang, Haihong, Liu, Qiongguang, Liu, Fengquan, Chang, Changqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108719/
https://www.ncbi.nlm.nih.gov/pubmed/35586864
http://dx.doi.org/10.3389/fmicb.2022.887967
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author Li, Kaihuai
Liao, Jinxing
Wei, Ming
Qiu, Shanxu
Wu, Weiyin
Zhao, Yancun
Wang, Haihong
Liu, Qiongguang
Liu, Fengquan
Chang, Changqing
author_facet Li, Kaihuai
Liao, Jinxing
Wei, Ming
Qiu, Shanxu
Wu, Weiyin
Zhao, Yancun
Wang, Haihong
Liu, Qiongguang
Liu, Fengquan
Chang, Changqing
author_sort Li, Kaihuai
collection PubMed
description Bacteria can withstand various types of environmental osmostress. A sudden rise in osmostress affects bacterial cell growth that is countered by activating special genes. The change of osmostress is generally a slow process under the natural environment. However, the collective response of bacteria to low osmostress remains unknown. This study revealed that the deletion of phoP (ΔphoP) from X. citri significantly compromised the growth and virulence as compared to the wild-type strain. Interestingly, low osmostress reversed physiological deficiencies of X. citri phoP mutant related to bacterial growth and virulence. The results also provided biochemical and genetic evidence that the physiological deficiency of phoP mutant can be reversed by low osmostress induced β-glucosidase (BglS) expression. Based on the data, this study proposes a novel regulatory mechanism of a novel β-glucosidase activation in X. citri through low osmostress to reverse the fitness deficiency.
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spelling pubmed-91087192022-05-17 The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress Li, Kaihuai Liao, Jinxing Wei, Ming Qiu, Shanxu Wu, Weiyin Zhao, Yancun Wang, Haihong Liu, Qiongguang Liu, Fengquan Chang, Changqing Front Microbiol Microbiology Bacteria can withstand various types of environmental osmostress. A sudden rise in osmostress affects bacterial cell growth that is countered by activating special genes. The change of osmostress is generally a slow process under the natural environment. However, the collective response of bacteria to low osmostress remains unknown. This study revealed that the deletion of phoP (ΔphoP) from X. citri significantly compromised the growth and virulence as compared to the wild-type strain. Interestingly, low osmostress reversed physiological deficiencies of X. citri phoP mutant related to bacterial growth and virulence. The results also provided biochemical and genetic evidence that the physiological deficiency of phoP mutant can be reversed by low osmostress induced β-glucosidase (BglS) expression. Based on the data, this study proposes a novel regulatory mechanism of a novel β-glucosidase activation in X. citri through low osmostress to reverse the fitness deficiency. Frontiers Media S.A. 2022-05-02 /pmc/articles/PMC9108719/ /pubmed/35586864 http://dx.doi.org/10.3389/fmicb.2022.887967 Text en Copyright © 2022 Li, Liao, Wei, Qiu, Wu, Zhao, Wang, Liu, Liu and Chang. 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
Li, Kaihuai
Liao, Jinxing
Wei, Ming
Qiu, Shanxu
Wu, Weiyin
Zhao, Yancun
Wang, Haihong
Liu, Qiongguang
Liu, Fengquan
Chang, Changqing
The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress
title The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress
title_full The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress
title_fullStr The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress
title_full_unstemmed The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress
title_short The Xanthomonas citri Reverse Fitness Deficiency by Activating a Novel β-Glucosidase Under Low Osmostress
title_sort xanthomonas citri reverse fitness deficiency by activating a novel β-glucosidase under low osmostress
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108719/
https://www.ncbi.nlm.nih.gov/pubmed/35586864
http://dx.doi.org/10.3389/fmicb.2022.887967
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