| Literature DB >> 26082024 |
Chiu-Lien Hung1,2, Hsin-Hung Cheng2, Wan-Chen Hsieh2, Zing Tsung-Yeh Tsai3, Huai-Kuang Tsai3, Chia-Han Chu4, Wen-Ping Hsieh5, Yi-Fan Chen2, Yu Tsou2, Chih-Ho Lai6,7,8, Wen-Ching Wang2,4.
Abstract
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.Entities:
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Year: 2015 PMID: 26082024 DOI: 10.1111/mmi.13089
Source DB: PubMed Journal: Mol Microbiol ISSN: 0950-382X Impact factor: 3.501