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Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ

The two-component signal transduction system PhoP/PhoQ is an important regulator for stress responses and virulence in most Gram-negative bacteria, but characterization of PhoP/PhoQ in Shigella has not been thoroughly investigated. In the present study, we found that deletion of phoPQ (ΔphoPQ) from...

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Autores principales: Lin, Zhiwei, Cai, Xia, Chen, Mingliang, Ye, Lina, Wu, Yang, Wang, Xiaofei, Lv, Zhihui, Shang, Yongpeng, Qu, Di
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775216/
https://www.ncbi.nlm.nih.gov/pubmed/29379483
http://dx.doi.org/10.3389/fmicb.2017.02689
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author Lin, Zhiwei
Cai, Xia
Chen, Mingliang
Ye, Lina
Wu, Yang
Wang, Xiaofei
Lv, Zhihui
Shang, Yongpeng
Qu, Di
author_facet Lin, Zhiwei
Cai, Xia
Chen, Mingliang
Ye, Lina
Wu, Yang
Wang, Xiaofei
Lv, Zhihui
Shang, Yongpeng
Qu, Di
author_sort Lin, Zhiwei
collection PubMed
description The two-component signal transduction system PhoP/PhoQ is an important regulator for stress responses and virulence in most Gram-negative bacteria, but characterization of PhoP/PhoQ in Shigella has not been thoroughly investigated. In the present study, we found that deletion of phoPQ (ΔphoPQ) from Shigella flexneri 2a 301 (Sf301) resulted in a significant decline (reduced by more than 15-fold) in invasion of HeLa cells and Caco-2 cells, and less inflammation (− or +) compared to Sf301 (+++) in the guinea pig Sereny test. In low Mg(2+) (10 μM) medium or pH 5 medium, the ΔphoPQ strain exhibited a growth deficiency compared to Sf301. The ΔphoPQ strain was more sensitive than Sf301 to polymyxin B, an important antimicrobial agent for treating multi-resistant Gram-negative infections. By comparing the transcriptional profiles of ΔphoPQ and Sf301 using DNA microarrays, 117 differentially expressed genes (DEGs) were identified, which were involved in Mg(2+) transport, lipopolysaccharide modification, acid resistance, bacterial virulence, respiratory, and energy metabolism. Based on the reported PhoP box motif [(T/G) GTTTA-5nt-(T/G) GTTTA], we screened 38 suspected PhoP target operons in S. flexneri, and 11 of them (phoPQ, mgtA, slyB, yoaE, yrbL, icsA, yhiWX, rstA, hdeAB, pagP, and shf–rfbU-virK-msbB2) were demonstrated to be PhoP-regulated genes based on electrophoretic mobility shift assays and β-galactosidase assays. One of these PhoP-regulated genes, icsA, is a well-known virulence factor in S. flexneri. In conclusion, our data suggest that the PhoP/PhoQ system modulates S. flexneri virulence (in an icsA-dependent manner) and stress responses of Mg(2+), pH and antibacterial peptides.
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spelling pubmed-57752162018-01-29 Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ Lin, Zhiwei Cai, Xia Chen, Mingliang Ye, Lina Wu, Yang Wang, Xiaofei Lv, Zhihui Shang, Yongpeng Qu, Di Front Microbiol Microbiology The two-component signal transduction system PhoP/PhoQ is an important regulator for stress responses and virulence in most Gram-negative bacteria, but characterization of PhoP/PhoQ in Shigella has not been thoroughly investigated. In the present study, we found that deletion of phoPQ (ΔphoPQ) from Shigella flexneri 2a 301 (Sf301) resulted in a significant decline (reduced by more than 15-fold) in invasion of HeLa cells and Caco-2 cells, and less inflammation (− or +) compared to Sf301 (+++) in the guinea pig Sereny test. In low Mg(2+) (10 μM) medium or pH 5 medium, the ΔphoPQ strain exhibited a growth deficiency compared to Sf301. The ΔphoPQ strain was more sensitive than Sf301 to polymyxin B, an important antimicrobial agent for treating multi-resistant Gram-negative infections. By comparing the transcriptional profiles of ΔphoPQ and Sf301 using DNA microarrays, 117 differentially expressed genes (DEGs) were identified, which were involved in Mg(2+) transport, lipopolysaccharide modification, acid resistance, bacterial virulence, respiratory, and energy metabolism. Based on the reported PhoP box motif [(T/G) GTTTA-5nt-(T/G) GTTTA], we screened 38 suspected PhoP target operons in S. flexneri, and 11 of them (phoPQ, mgtA, slyB, yoaE, yrbL, icsA, yhiWX, rstA, hdeAB, pagP, and shf–rfbU-virK-msbB2) were demonstrated to be PhoP-regulated genes based on electrophoretic mobility shift assays and β-galactosidase assays. One of these PhoP-regulated genes, icsA, is a well-known virulence factor in S. flexneri. In conclusion, our data suggest that the PhoP/PhoQ system modulates S. flexneri virulence (in an icsA-dependent manner) and stress responses of Mg(2+), pH and antibacterial peptides. Frontiers Media S.A. 2018-01-15 /pmc/articles/PMC5775216/ /pubmed/29379483 http://dx.doi.org/10.3389/fmicb.2017.02689 Text en Copyright © 2018 Lin, Cai, Chen, Ye, Wu, Wang, Lv, Shang and Qu. 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
Lin, Zhiwei
Cai, Xia
Chen, Mingliang
Ye, Lina
Wu, Yang
Wang, Xiaofei
Lv, Zhihui
Shang, Yongpeng
Qu, Di
Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ
title Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ
title_full Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ
title_fullStr Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ
title_full_unstemmed Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ
title_short Virulence and Stress Responses of Shigella flexneri Regulated by PhoP/PhoQ
title_sort virulence and stress responses of shigella flexneri regulated by phop/phoq
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775216/
https://www.ncbi.nlm.nih.gov/pubmed/29379483
http://dx.doi.org/10.3389/fmicb.2017.02689
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