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:...
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Veröffentlicht in: | Gut and liver 2018-01, Vol.12 (1), p.51 |
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creator | Thein Myint Muhammad Miftahussurur Ratha-korn Vilaichone New Ni Than Than Aye Phawinee Subsomwong Tomohisa Uchida Varocha Mahachai Yoshio Yamaoka |
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. (Gut Liver 2018;12:51-57) |
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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. (Gut Liver 2018;12:51-57)</description><identifier>ISSN: 1976-2283</identifier><language>kor</language><publisher>대한소화기학회</publisher><subject>cagA ; Helicobacter pylori ; Myanmar</subject><ispartof>Gut and liver, 2018-01, Vol.12 (1), p.51</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Thein Myint</creatorcontrib><creatorcontrib>Muhammad Miftahussurur</creatorcontrib><creatorcontrib>Ratha-korn Vilaichone</creatorcontrib><creatorcontrib>New Ni</creatorcontrib><creatorcontrib>Than Than Aye</creatorcontrib><creatorcontrib>Phawinee Subsomwong</creatorcontrib><creatorcontrib>Tomohisa Uchida</creatorcontrib><creatorcontrib>Varocha Mahachai</creatorcontrib><creatorcontrib>Yoshio Yamaoka</creatorcontrib><title>Characterizing Helicobacter pylori cagA in Myanmar</title><title>Gut and liver</title><addtitle>Gut and Liver</addtitle><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. (Gut Liver 2018;12:51-57)</description><subject>cagA</subject><subject>Helicobacter pylori</subject><subject>Myanmar</subject><issn>1976-2283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpjYeA0tDQ30zUysjDmYOAqLs4yMDAzNDI35WQwcs5ILEpMLkktyqzKzEtX8EjNyUzOTwKLKBRU5uQXZSokJ6Y7KmTmKfhWJublJhbxMLCmJeYUp_JCaW4GaTfXEGcP3ezM4uL4gqJMoJrKeGNTM3NTUyNj_LIAVZ8toA</recordid><startdate>20180130</startdate><enddate>20180130</enddate><creator>Thein Myint</creator><creator>Muhammad Miftahussurur</creator><creator>Ratha-korn Vilaichone</creator><creator>New Ni</creator><creator>Than Than Aye</creator><creator>Phawinee Subsomwong</creator><creator>Tomohisa Uchida</creator><creator>Varocha Mahachai</creator><creator>Yoshio Yamaoka</creator><general>대한소화기학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20180130</creationdate><title>Characterizing Helicobacter pylori cagA in Myanmar</title><author>Thein Myint ; Muhammad Miftahussurur ; Ratha-korn Vilaichone ; New Ni ; Than Than Aye ; Phawinee Subsomwong ; Tomohisa Uchida ; Varocha Mahachai ; Yoshio Yamaoka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_35675523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2018</creationdate><topic>cagA</topic><topic>Helicobacter pylori</topic><topic>Myanmar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thein Myint</creatorcontrib><creatorcontrib>Muhammad Miftahussurur</creatorcontrib><creatorcontrib>Ratha-korn Vilaichone</creatorcontrib><creatorcontrib>New Ni</creatorcontrib><creatorcontrib>Than Than Aye</creatorcontrib><creatorcontrib>Phawinee Subsomwong</creatorcontrib><creatorcontrib>Tomohisa Uchida</creatorcontrib><creatorcontrib>Varocha Mahachai</creatorcontrib><creatorcontrib>Yoshio Yamaoka</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Gut and liver</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thein Myint</au><au>Muhammad Miftahussurur</au><au>Ratha-korn Vilaichone</au><au>New Ni</au><au>Than Than Aye</au><au>Phawinee Subsomwong</au><au>Tomohisa Uchida</au><au>Varocha Mahachai</au><au>Yoshio Yamaoka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterizing Helicobacter pylori cagA in Myanmar</atitle><jtitle>Gut and liver</jtitle><addtitle>Gut and Liver</addtitle><date>2018-01-30</date><risdate>2018</risdate><volume>12</volume><issue>1</issue><spage>51</spage><pages>51-</pages><issn>1976-2283</issn><abstract>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. (Gut Liver 2018;12:51-57)</abstract><pub>대한소화기학회</pub><tpages>7</tpages></addata></record> |
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source | KoreaMed Open Access; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | cagA Helicobacter pylori Myanmar |
title | Characterizing Helicobacter pylori cagA in Myanmar |
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