{"title":"利用高灵敏度实时PCR技术鉴定胃活检组织中幽门螺杆菌和cagA基因型","authors":"Shiho Yamazaki , Shunji Kato , Norio Matsukura , Masahiro Ohtani , Yoshiyuki Ito , Hiroyuki Suto , Yukinao Yamazaki , Akiyo Yamakawa , Shinkan Tokudome , Hideaki Higashi , Masanori Hatakeyama , Takeshi Azuma","doi":"10.1016/j.femsim.2004.12.011","DOIUrl":null,"url":null,"abstract":"<div><p><span>The CagA<span> protein is one of the virulence factors of </span></span><span><em>Helicobacter </em><em>pylori</em></span><span>, and two major subtypes of CagA have been observed, the Western and East Asian type. CagA is injected from the bacteria into gastric epithelial cells, undergoes tyrosine phosphorylation, and binds to Src homology 2 domain-containing protein-tyrosine phosphatase SHP-2. The East Asian type CagA binds to SHP-2 more strongly than the Western type CagA. Here, we tried to distinguish the CagA type by highly sensitive real-time PCR with the objective of establishing a system to detect </span><em>H. pylori</em><span> and CagA subtypes from gastric biopsies. We designed primers and probe sets for Western or East Asian-</span><em>cagA</em> at Western-specific or East Asian-specific sequence regions, respectively, and <em>H. pylori</em><span> 16S rRNA. We could detect the </span><em>H. pylori</em> 16S rRNA gene, Western and East Asian-<em>cagA</em> gene from DNA of gastric biopsies. The sensitivity and specificity for <em>H. pylori</em> infection was 100% in this system. In Thai patients, 87.8% (36/41) were <em>cagA</em>-positive; 26.8% (11/41) were Western-<em>cagA</em> positive and 53.7% (22/41) were East Asian-<em>cagA</em> positive, while 7.3% (3/41) reacted with both types of <em>cagA</em>. These results suggest that this real-time PCR system provides a highly sensitive assessment of CagA type as a new diagnostic tool for the pathogenicity of <em>H. pylori</em> infection.</p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2005-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2004.12.011","citationCount":"29","resultStr":"{\"title\":\"Identification of Helicobacter pylori and the cagA genotype in gastric biopsies using highly sensitive real-time PCR as a new diagnostic tool\",\"authors\":\"Shiho Yamazaki , Shunji Kato , Norio Matsukura , Masahiro Ohtani , Yoshiyuki Ito , Hiroyuki Suto , Yukinao Yamazaki , Akiyo Yamakawa , Shinkan Tokudome , Hideaki Higashi , Masanori Hatakeyama , Takeshi Azuma\",\"doi\":\"10.1016/j.femsim.2004.12.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>The CagA<span> protein is one of the virulence factors of </span></span><span><em>Helicobacter </em><em>pylori</em></span><span>, and two major subtypes of CagA have been observed, the Western and East Asian type. CagA is injected from the bacteria into gastric epithelial cells, undergoes tyrosine phosphorylation, and binds to Src homology 2 domain-containing protein-tyrosine phosphatase SHP-2. The East Asian type CagA binds to SHP-2 more strongly than the Western type CagA. Here, we tried to distinguish the CagA type by highly sensitive real-time PCR with the objective of establishing a system to detect </span><em>H. pylori</em><span> and CagA subtypes from gastric biopsies. We designed primers and probe sets for Western or East Asian-</span><em>cagA</em> at Western-specific or East Asian-specific sequence regions, respectively, and <em>H. pylori</em><span> 16S rRNA. We could detect the </span><em>H. pylori</em> 16S rRNA gene, Western and East Asian-<em>cagA</em> gene from DNA of gastric biopsies. The sensitivity and specificity for <em>H. pylori</em> infection was 100% in this system. In Thai patients, 87.8% (36/41) were <em>cagA</em>-positive; 26.8% (11/41) were Western-<em>cagA</em> positive and 53.7% (22/41) were East Asian-<em>cagA</em> positive, while 7.3% (3/41) reacted with both types of <em>cagA</em>. These results suggest that this real-time PCR system provides a highly sensitive assessment of CagA type as a new diagnostic tool for the pathogenicity of <em>H. pylori</em> infection.</p></div>\",\"PeriodicalId\":12220,\"journal\":{\"name\":\"FEMS immunology and medical microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.femsim.2004.12.011\",\"citationCount\":\"29\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FEMS immunology and medical microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0928824405000040\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEMS immunology and medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928824405000040","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Identification of Helicobacter pylori and the cagA genotype in gastric biopsies using highly sensitive real-time PCR as a new diagnostic tool
The CagA protein is one of the virulence factors of Helicobacter pylori, and two major subtypes of CagA have been observed, the Western and East Asian type. CagA is injected from the bacteria into gastric epithelial cells, undergoes tyrosine phosphorylation, and binds to Src homology 2 domain-containing protein-tyrosine phosphatase SHP-2. The East Asian type CagA binds to SHP-2 more strongly than the Western type CagA. Here, we tried to distinguish the CagA type by highly sensitive real-time PCR with the objective of establishing a system to detect H. pylori and CagA subtypes from gastric biopsies. We designed primers and probe sets for Western or East Asian-cagA at Western-specific or East Asian-specific sequence regions, respectively, and H. pylori 16S rRNA. We could detect the H. pylori 16S rRNA gene, Western and East Asian-cagA gene from DNA of gastric biopsies. The sensitivity and specificity for H. pylori infection was 100% in this system. In Thai patients, 87.8% (36/41) were cagA-positive; 26.8% (11/41) were Western-cagA positive and 53.7% (22/41) were East Asian-cagA positive, while 7.3% (3/41) reacted with both types of cagA. These results suggest that this real-time PCR system provides a highly sensitive assessment of CagA type as a new diagnostic tool for the pathogenicity of H. pylori infection.