Mohamed Ramelah , Ahmad Aminuddin , Hanafiah Alfizah , Mohd Rose Isa , Ali Yaakob Jasmi , Huck Joo Tan , A. Jamal A. Rahman , Abdul Manap Rizal , M. Zawawi Mazlam
{"title":"cagA gene variants in Malaysian Helicobacter pylori strains isolated from patients of different ethnic groups","authors":"Mohamed Ramelah , Ahmad Aminuddin , Hanafiah Alfizah , Mohd Rose Isa , Ali Yaakob Jasmi , Huck Joo Tan , A. Jamal A. Rahman , Abdul Manap Rizal , M. Zawawi Mazlam","doi":"10.1016/j.femsim.2005.02.001","DOIUrl":null,"url":null,"abstract":"<div><p><span><em>Helicobacter </em><em>pylori</em></span> infection of a distinct subtype of <span><em>cagA</em></span> may lead to different pathological manifestation. The aim of this study is to determine the presence of <em>cagA</em> gene and its variants in <em>H. pylori</em> infection among different ethnic groups and its effect on gastroduodenal diseases. Overall detection of <em>cagA</em> among the 205 clinical isolates of <em>H. pylori</em> was 94%. Variations in size of the 3′ region of <em>cagA</em> gene were examined among 192 Malaysian <em>H. pylori cagA</em>-positive strains. Results showed that three <em>cagA</em> variants differing in fragment length of PCR products were detected and designated as type A (621–651<!--> <!-->bp), type B (732–735<!--> <!-->bp) and type C (525 bp). Although there was no association between any of the <em>cagA</em><span> subtypes with peptic ulcer disease (</span><em>p</em> <!-->><!--> <!-->0.05), an association between <em>cagA</em> subtypes with a specific ethnic group was observed. Specific-<em>cagA</em> subtype A strains were predominantly isolated from Chinese compared to Malays and Indians (<em>p</em> <!--><<!--> <!-->0.0005), and <em>cagA</em> subtype B strains were predominantly isolated from Malays and Indians compared to Chinese (<em>p</em> <!--><<!--> <!-->0.05). The <em>cagA</em> type A strains of <em>H. pylori</em> is commonly found in the Chinese patients who have a higher risk of peptic ulcer disease, thus indicating that it could be used as an important clinical biomarker for a more severe infection.</p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2005-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.02.001","citationCount":"28","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEMS immunology and medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928824405000428","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 28
Abstract
Helicobacter pylori infection of a distinct subtype of cagA may lead to different pathological manifestation. The aim of this study is to determine the presence of cagA gene and its variants in H. pylori infection among different ethnic groups and its effect on gastroduodenal diseases. Overall detection of cagA among the 205 clinical isolates of H. pylori was 94%. Variations in size of the 3′ region of cagA gene were examined among 192 Malaysian H. pylori cagA-positive strains. Results showed that three cagA variants differing in fragment length of PCR products were detected and designated as type A (621–651 bp), type B (732–735 bp) and type C (525 bp). Although there was no association between any of the cagA subtypes with peptic ulcer disease (p > 0.05), an association between cagA subtypes with a specific ethnic group was observed. Specific-cagA subtype A strains were predominantly isolated from Chinese compared to Malays and Indians (p < 0.0005), and cagA subtype B strains were predominantly isolated from Malays and Indians compared to Chinese (p < 0.05). The cagA type A strains of H. pylori is commonly found in the Chinese patients who have a higher risk of peptic ulcer disease, thus indicating that it could be used as an important clinical biomarker for a more severe infection.