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CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer

Objective: The aim of study was to determine relationship between cagA and genetic characterization of metronidazole (MTZ) resistant H. pylori strains from a region at high risk of gastric cancer. Methods: 172 H. pylori strains were isolated from the patients with dyspeptic symptoms, and antimicrobi...

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Autores principales: Yue, Jin-Yong, Yue, Jing, Wang, Ming-Yi, Song, Wen-chong, Gao, Xiao-Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publicaitons 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121702/
https://www.ncbi.nlm.nih.gov/pubmed/25097521
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author Yue, Jin-Yong
Yue, Jing
Wang, Ming-Yi
Song, Wen-chong
Gao, Xiao-Zhong
author_facet Yue, Jin-Yong
Yue, Jing
Wang, Ming-Yi
Song, Wen-chong
Gao, Xiao-Zhong
author_sort Yue, Jin-Yong
collection PubMed
description Objective: The aim of study was to determine relationship between cagA and genetic characterization of metronidazole (MTZ) resistant H. pylori strains from a region at high risk of gastric cancer. Methods: 172 H. pylori strains were isolated from the patients with dyspeptic symptoms, and antimicrobial susceptibility testing for MTZ was assessed by E-test. rdxA and frxA genes were amplified using PCR among the MTZ resistant isolates. The status of the plasmid and classes 1~3 integrons were investigated in all isolates. Results: MTZ was detected in 88 isolates (51.16%). Variations in the rdxA gene leading to alterations of amino acids in RdxA proteins were identified in all MTZ resistant strains. FrxA contained missense alterations in 55 MTZ resistant isolates, while the premature truncation of FrxA was caused by frameshift mutations in 9 MTZ resistant strains. Plasmid was found in one MTZ sensitive strain (0.58%), and none of Class 1~3 integrases gene was detected in the studied isolates. The conservative cagA fragment was obtained from all clinical isolates of H. pylori. The sequence of cagA 3' variable region in 164 strains were obtained, including East Asian-type (122, 74.39%) and Western-type (42, 25.61%). Prevalence of Western-type cagA 3' variable region was significantly higher in MTZ resistant (33.73%, 28/83) than those of MTZ-sensitive strains (17.28%, 14/81) (p=0.02). Conclusion: A high prevalence of MTZ resistance was found in the region, and bacterial chromosome mutations in the rdxA and frxA gene still contribute to the high-level MTZ resistance. H. pylori strains characterized with West-type cagA 3’ variable region tend to acquire MTZ resistance in the region.
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spelling pubmed-41217022014-08-05 CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer Yue, Jin-Yong Yue, Jing Wang, Ming-Yi Song, Wen-chong Gao, Xiao-Zhong Pak J Med Sci Original Article Objective: The aim of study was to determine relationship between cagA and genetic characterization of metronidazole (MTZ) resistant H. pylori strains from a region at high risk of gastric cancer. Methods: 172 H. pylori strains were isolated from the patients with dyspeptic symptoms, and antimicrobial susceptibility testing for MTZ was assessed by E-test. rdxA and frxA genes were amplified using PCR among the MTZ resistant isolates. The status of the plasmid and classes 1~3 integrons were investigated in all isolates. Results: MTZ was detected in 88 isolates (51.16%). Variations in the rdxA gene leading to alterations of amino acids in RdxA proteins were identified in all MTZ resistant strains. FrxA contained missense alterations in 55 MTZ resistant isolates, while the premature truncation of FrxA was caused by frameshift mutations in 9 MTZ resistant strains. Plasmid was found in one MTZ sensitive strain (0.58%), and none of Class 1~3 integrases gene was detected in the studied isolates. The conservative cagA fragment was obtained from all clinical isolates of H. pylori. The sequence of cagA 3' variable region in 164 strains were obtained, including East Asian-type (122, 74.39%) and Western-type (42, 25.61%). Prevalence of Western-type cagA 3' variable region was significantly higher in MTZ resistant (33.73%, 28/83) than those of MTZ-sensitive strains (17.28%, 14/81) (p=0.02). Conclusion: A high prevalence of MTZ resistance was found in the region, and bacterial chromosome mutations in the rdxA and frxA gene still contribute to the high-level MTZ resistance. H. pylori strains characterized with West-type cagA 3’ variable region tend to acquire MTZ resistance in the region. Professional Medical Publicaitons 2014 /pmc/articles/PMC4121702/ /pubmed/25097521 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yue, Jin-Yong
Yue, Jing
Wang, Ming-Yi
Song, Wen-chong
Gao, Xiao-Zhong
CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer
title CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer
title_full CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer
title_fullStr CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer
title_full_unstemmed CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer
title_short CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer
title_sort caga status & genetic characterization of metronidazole resistant strains of h. pylori from: a region at high risk of gastric cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121702/
https://www.ncbi.nlm.nih.gov/pubmed/25097521
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