The CrdRS two‐component system in Helicobacter pylori responds to nitrosative stress

Summary Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two‐component systems (TCSs) that enable its persistent colonization. The aim of this study was to investigate whether any of the three paired TCSs (ArsRS, FleRS and CrdRS) in H. pylori res...

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Published inMolecular microbiology Vol. 97; no. 6; pp. 1128 - 1141
Main Authors Hung, Chiu‐Lien, Cheng, Hsin‐Hung, Hsieh, Wan‐Chen, Tsai, Zing Tsung‐Yeh, Tsai, Huai‐Kuang, Chu, Chia‐Han, Hsieh, Wen‐Ping, Chen, Yi‐Fan, Tsou, Yu, Lai, Chih‐Ho, Wang, Wen‐Ching
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.09.2015
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Abstract Summary Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two‐component systems (TCSs) that enable its persistent colonization. The aim of this study was to investigate whether any of the three paired TCSs (ArsRS, FleRS and CrdRS) in H. pylori respond to nitrosative stress. The results showed that the expression of crdS was significantly increased upon exposure to nitric oxide (NO). crdS‐knockout (ΔcrdS) and crdR/crdS‐knockout (ΔcrdRS) H. pylori, but not arsS‐knockout (ΔarsS) or fleS‐knockout (ΔfleS) H. pylori, showed a significant loss of viability upon exposure to NO compared with wild‐type strain. Knockin crdS (ΔcrdS‐in) significantly restored viability in the presence of NO. Global transcriptional profiling analysis of wild‐type and ΔcrdS H. pylori in the presence or absence of NO showed that 101 genes were differentially expressed, including copper resistance determinant A (crdA), transport, binding and envelope proteins. The CrdR binding motifs were investigated by competitive electrophoretic mobility shift assay, which revealed that the two AC‐rich regions in the crdA promoter region are required for binding. These results demonstrate that CrdR–crdA interaction enables H. pylori to survive under nitrosative stress. Helicobacter pylori successfully responds and adapts to various stresses from gastric environment via its three‐pair two‐component systems (TCSs). This report shows that a unique TCS, CrdRS, functions as a sensor for nitrosative stress. Nitrosative challenge differentially upregulates the expression of resistance determinant A (crdA). Further, CrdR binds to the proximal promoter region of crdA that consists of a two AC‐rich region. These findings demonstrate that CrdR‐crdA interaction enables H. pylori to survive under nitrosative stress.
AbstractList Summary Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two‐component systems (TCSs) that enable its persistent colonization. The aim of this study was to investigate whether any of the three paired TCSs (ArsRS, FleRS and CrdRS) in H. pylori respond to nitrosative stress. The results showed that the expression of crdS was significantly increased upon exposure to nitric oxide (NO). crdS‐knockout (ΔcrdS) and crdR/crdS‐knockout (ΔcrdRS) H. pylori, but not arsS‐knockout (ΔarsS) or fleS‐knockout (ΔfleS) H. pylori, showed a significant loss of viability upon exposure to NO compared with wild‐type strain. Knockin crdS (ΔcrdS‐in) significantly restored viability in the presence of NO. Global transcriptional profiling analysis of wild‐type and ΔcrdS H. pylori in the presence or absence of NO showed that 101 genes were differentially expressed, including copper resistance determinant A (crdA), transport, binding and envelope proteins. The CrdR binding motifs were investigated by competitive electrophoretic mobility shift assay, which revealed that the two AC‐rich regions in the crdA promoter region are required for binding. These results demonstrate that CrdR–crdA interaction enables H. pylori to survive under nitrosative stress. Helicobacter pylori successfully responds and adapts to various stresses from gastric environment via its three‐pair two‐component systems (TCSs). This report shows that a unique TCS, CrdRS, functions as a sensor for nitrosative stress. Nitrosative challenge differentially upregulates the expression of resistance determinant A (crdA). Further, CrdR binds to the proximal promoter region of crdA that consists of a two AC‐rich region. These findings demonstrate that CrdR‐crdA interaction enables H. pylori to survive under nitrosative stress.
Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two-component systems (TCSs) that enable its persistent colonization. The aim of this study was to investigate whether any of the three paired TCSs (ArsRS, FleRS and CrdRS) in H. pylori respond to nitrosative stress. The results showed that the expression of crdS was significantly increased upon exposure to nitric oxide (NO). crdS-knockout (...crdS) and crdR/crdS-knockout (...crdRS) H. pylori, but not arsS-knockout (...arsS) or fleS-knockout (...fleS) H. pylori, showed a significant loss of viability upon exposure to NO compared with wild-type strain. Knockin crdS (...crdS-in) significantly restored viability in the presence of NO. Global transcriptional profiling analysis of wild-type and ...crdS H. pylori in the presence or absence of NO showed that 101 genes were differentially expressed, including copper resistance determinant A (crdA), transport, binding and envelope proteins. The CrdR binding motifs were investigated by competitive electrophoretic mobility shift assay, which revealed that the two AC-rich regions in the crdA promoter region are required for binding. These results demonstrate that CrdR-crdA interaction enables H. pylori to survive under nitrosative stress. (ProQuest: ... denotes formulae/symbols omitted.)
Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two-component systems (TCSs) that enable its persistent colonization. The aim of this study was to investigate whether any of the three paired TCSs (ArsRS, FleRS and CrdRS) in H. pylori respond to nitrosative stress. The results showed that the expression of crdS was significantly increased upon exposure to nitric oxide (NO). crdS-knockout (ΔcrdS) and crdR/crdS-knockout (ΔcrdRS) H. pylori, but not arsS-knockout (ΔarsS) or fleS-knockout (ΔfleS) H. pylori, showed a significant loss of viability upon exposure to NO compared with wild-type strain. Knockin crdS (ΔcrdS-in) significantly restored viability in the presence of NO. Global transcriptional profiling analysis of wild-type and ΔcrdS H. pylori in the presence or absence of NO showed that 101 genes were differentially expressed, including copper resistance determinant A (crdA), transport, binding and envelope proteins. The CrdR binding motifs were investigated by competitive electrophoretic mobility shift assay, which revealed that the two AC-rich regions in the crdA promoter region are required for binding. These results demonstrate that CrdR-crdA interaction enables H. pylori to survive under nitrosative stress.
Author Wang, Wen‐Ching
Chu, Chia‐Han
Tsai, Zing Tsung‐Yeh
Hsieh, Wan‐Chen
Cheng, Hsin‐Hung
Tsai, Huai‐Kuang
Chen, Yi‐Fan
Tsou, Yu
Hsieh, Wen‐Ping
Lai, Chih‐Ho
Hung, Chiu‐Lien
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  organization: Chang Gung University
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  surname: Wang
  fullname: Wang, Wen‐Ching
  organization: National Tsing Hua University
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Snippet Summary Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two‐component systems (TCSs) that enable its...
Helicobacter pylori inhabits the gastric mucosa where it senses and responds to various stresses via a two-component systems (TCSs) that enable its persistent...
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wiley
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SubjectTerms Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Base Sequence
Copper - metabolism
DNA-Binding Proteins - metabolism
Gene expression
Gene Expression Profiling
Gene Knockout Techniques
Gram-negative bacteria
Helicobacter pylori - genetics
Helicobacter pylori - metabolism
Molecular Sequence Data
Nitric oxide
Nitric Oxide - metabolism
Promoter Regions, Genetic
Proteins
Stress, Physiological
Title The CrdRS two‐component system in Helicobacter pylori responds to nitrosative stress
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fmmi.13089
https://www.ncbi.nlm.nih.gov/pubmed/26082024
https://www.proquest.com/docview/1713596574/abstract/
https://search.proquest.com/docview/1711537326
Volume 97
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