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Characterizing Helicobacter pylori cagA in Myanmar
BACKGROUND/AIMS: Differences in the Helicobacter pylori infection rate are not sufficient to clarify the dissimilarity of gastric cancer incidence between Myanmar and its neighboring countries. To better understand this trend, the H. pylori virulence gene cagA was characterized in Myanmar. METHODS:...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Office of Gut and Liver
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753684/ https://www.ncbi.nlm.nih.gov/pubmed/29069889 http://dx.doi.org/10.5009/gnl17053 |
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author | Myint, Thein Miftahussurur, Muhammad Vilaichone, Ratha-korn Ni, New Aye, Than Than Subsomwong, Phawinee Uchida, Tomohisa Mahachai, Varocha Yamaoka, Yoshio |
author_facet | Myint, Thein Miftahussurur, Muhammad Vilaichone, Ratha-korn Ni, New Aye, Than Than Subsomwong, Phawinee Uchida, Tomohisa Mahachai, Varocha Yamaoka, Yoshio |
author_sort | Myint, Thein |
collection | PubMed |
description | BACKGROUND/AIMS: Differences in the Helicobacter pylori infection rate are not sufficient to clarify the dissimilarity of gastric cancer incidence between Myanmar and its neighboring countries. To better understand this trend, the H. pylori virulence gene cagA was characterized in Myanmar. METHODS: Glutamate-proline-isoleucine-tyrosine-alanine (EPIYA) patterns and CagA multimerization (CM) motifs of cagA genotypes were examined by performing polymerase chain reactions and DNA sequencing. RESULTS: Of 69 tested H. pylori strains, cagA-positive patients had significantly more severe histological scores in their antrum than cagA-negative patients. Sequence analysis revealed that 94.1% of strains had Western-type cagA containing an EPIYA motif (92.6%) or EPIYT motif (6.4%). The intestinal metaplasia scores in the antral of patients infected with the ABC and ABCC types of cagA were significantly higher than those of patients with AB-type cagA. Interestingly, in patients infected with H. pylori, 46.3% of strains with three EPIYA motifs contained two identical Western-typical CM motifs, and these patients showed significantly higher antrum inflammation scores than patients infected with two identical nontypical-CM motif strains (p=0.02). CONCLUSIONS: In Myanmarese strains, Western-type cagA was predominant. The presence of CM motifs and the proportion of multiple EPIYA-C segments might partially explain the intermediate gastric cancer risk found in Myanmar. |
format | Online Article Text |
id | pubmed-5753684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Editorial Office of Gut and Liver |
record_format | MEDLINE/PubMed |
spelling | pubmed-57536842018-01-19 Characterizing Helicobacter pylori cagA in Myanmar Myint, Thein Miftahussurur, Muhammad Vilaichone, Ratha-korn Ni, New Aye, Than Than Subsomwong, Phawinee Uchida, Tomohisa Mahachai, Varocha Yamaoka, Yoshio Gut Liver Original Article BACKGROUND/AIMS: Differences in the Helicobacter pylori infection rate are not sufficient to clarify the dissimilarity of gastric cancer incidence between Myanmar and its neighboring countries. To better understand this trend, the H. pylori virulence gene cagA was characterized in Myanmar. METHODS: Glutamate-proline-isoleucine-tyrosine-alanine (EPIYA) patterns and CagA multimerization (CM) motifs of cagA genotypes were examined by performing polymerase chain reactions and DNA sequencing. RESULTS: Of 69 tested H. pylori strains, cagA-positive patients had significantly more severe histological scores in their antrum than cagA-negative patients. Sequence analysis revealed that 94.1% of strains had Western-type cagA containing an EPIYA motif (92.6%) or EPIYT motif (6.4%). The intestinal metaplasia scores in the antral of patients infected with the ABC and ABCC types of cagA were significantly higher than those of patients with AB-type cagA. Interestingly, in patients infected with H. pylori, 46.3% of strains with three EPIYA motifs contained two identical Western-typical CM motifs, and these patients showed significantly higher antrum inflammation scores than patients infected with two identical nontypical-CM motif strains (p=0.02). CONCLUSIONS: In Myanmarese strains, Western-type cagA was predominant. The presence of CM motifs and the proportion of multiple EPIYA-C segments might partially explain the intermediate gastric cancer risk found in Myanmar. Editorial Office of Gut and Liver 2018-01 2017-10-27 /pmc/articles/PMC5753684/ /pubmed/29069889 http://dx.doi.org/10.5009/gnl17053 Text en Copyright © 2018 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Myint, Thein Miftahussurur, Muhammad Vilaichone, Ratha-korn Ni, New Aye, Than Than Subsomwong, Phawinee Uchida, Tomohisa Mahachai, Varocha Yamaoka, Yoshio Characterizing Helicobacter pylori cagA in Myanmar |
title | Characterizing Helicobacter pylori cagA in Myanmar |
title_full | Characterizing Helicobacter pylori cagA in Myanmar |
title_fullStr | Characterizing Helicobacter pylori cagA in Myanmar |
title_full_unstemmed | Characterizing Helicobacter pylori cagA in Myanmar |
title_short | Characterizing Helicobacter pylori cagA in Myanmar |
title_sort | characterizing helicobacter pylori caga in myanmar |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753684/ https://www.ncbi.nlm.nih.gov/pubmed/29069889 http://dx.doi.org/10.5009/gnl17053 |
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