CagA 3' region polymorphism of Helicobacter pylori and its association with chronic gastritis in the Chinese population.

Xiaoyan Zhu, Chao Ma, Rina Sa, Yaxuan Wang, Chaohui Zhu, Yajiao Zhao, Juan Luo, Xiaochuan Liu
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Abstract

Introduction. Cytotoxin-associated gene A (CagA) from Helicobacter pylori is highly related to chronic gastritis. Tyrosine phosphorylation of Glu-Pro-Ile-Tyr-Ala (EPIYA) motifs from CagA determines the pathogenicity of H. pylori.Gap statement. The precise amino acid variations surrounding the EPIYA motifs and their correlation with clinical outcomes have been poorly explored.Aim. The purpose of this study was to examine the CagA 3' region polymorphism of H. pylori and its association with chronic gastritis in the Chinese population.Method. A total of 86 cagA-positive H. pylori strains were isolated from patients with chronic gastritis in two different hospitals in Beijing, PR China. Genomic DNA was extracted commercial kits, and the cagA 3' variable region of H. pylori was amplified by polymerase chain reaction (PCR). The PCR products were sequenced and analysed using the CLC Sequence Viewer, BioEdit, and WebLogo 3.Results. Two hundred and fifty-nine EPIYA motifs were identified from cagA-positive H. pylori strains. Notably, EPIYA-B exhibited a higher frequency of variation in comparison to EPIYA-A, EPIYA-C, and EPIYA-D. The prevalent sequences for East-Asian-type CagA were QVNK and TIDF, while KVNK and TIDD were most commonly observed for Western-type CagA. The CRPIA motifs of East-Asian-type CagA and Western-type CagA varied at positions 4, 6, 7, 8, and 10. CagA-ABD (73.2%) was the most prevalent type, followed by CagA-ABC (18.6%) and CagA-AB (3.4%). The ratio of CagA-ABD was observed to be higher in cases of chronic non-atrophic gastritis with erosive (NAGE) or chronic atrophic gastritis (AG) compared to chronic non-atrophic gastritis (NAG), and the difference was found to be statistically significant (χ2=59.000/64.000, P<0.001).Conclusions. The EPIYA segments of Western-type CagA and East-Asian-type CagA differ significantly and the presence of CagA-ABD may be associated with severe chronic gastritis from this study.

中国人群幽门螺杆菌 CagA 3' 区多态性及其与慢性胃炎的关系。
简介幽门螺杆菌的细胞毒素相关基因 A(CagA)与慢性胃炎密切相关。CagA的Glu-Pro-Ile-Tyr-Ala(EPIYA)基团的酪氨酸磷酸化决定了幽门螺杆菌的致病性。围绕 EPIYA 主题的精确氨基酸变异及其与临床结果的相关性尚未得到充分探讨。本研究旨在探讨中国人群中幽门螺杆菌 CagA 3' 区多态性及其与慢性胃炎的关系。从北京两家医院的慢性胃炎患者中分离出 86 株 cagA 阳性幽门螺杆菌。用商品化试剂盒提取基因组 DNA,并通过聚合酶链式反应(PCR)扩增幽门螺杆菌 cagA 3' 可变区。利用 CLC Sequence Viewer、BioEdit 和 WebLogo 3 对 PCR 产物进行测序和分析。从 cagA 阳性的幽门螺杆菌菌株中鉴定出 259 个 EPIYA 主题。值得注意的是,与 EPIYA-A、EPIYA-C 和 EPIYA-D 相比,EPIYA-B 的变异频率更高。东亚型 CagA 的常见序列是 QVNK 和 TIDF,而西洋型 CagA 最常见的序列是 KVNK 和 TIDD。东亚型 CagA 和西洋型 CagA 的 CRPIA 主题在第 4、6、7、8 和 10 位有所不同。CagA-ABD(73.2%)是最普遍的类型,其次是CagA-ABC(18.6%)和CagA-AB(3.4%)。与慢性非萎缩性胃炎(NAG)相比,慢性非萎缩性胃炎伴糜烂性胃炎(NAGE)或慢性萎缩性胃炎(AG)病例的 CagA-ABD 比率更高,差异具有统计学意义(χ2=59.000/64.000,PConclusions.本研究发现,西方型CagA和东亚型CagA的EPIYA片段差异显著,CagA-ABD的存在可能与严重的慢性胃炎有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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