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

Author:

Zhu Xiaoyan123ORCID,Ma Chao45,Sa Rina6,Wang Yaxuan7,Zhu Chaohui8,Zhao Yajiao9,Luo Juan1011,Liu Xiaochuan9

Affiliation:

1. Yunnan Key Laboratory of Laboratory Medicine, Kunming, PR China

2. Department of Clinical Laboratory, The First Affiliated Hospital of Kunming Medical University, Kunming, PR China

3. Yunnan Province Clinical Research Center for Laboratory Medicine, Kunming, PR China

4. Department of Clinical Laboratory, The Beijing Prevention and Treatment Hospital of Occupational Disease for Chemical Industry, Beijing, PR China

5. Beijing Institute of Occupational Disease Prevention and Treatment, Beijing, PR China

6. General internal medicine, Jingdong Medical Area, General Hospital of Chinese PLA, Beijing, PR China

7. National Center for Clinical Laboratories, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Hospital/National Center of Gerontology, Beijing, PR China

8. Department of Gastroenterology, The Eighth Medical Center of PLA General Hospital, Beijing, PR China

9. Department of Gastroenterology, Emergency General Hospital, Beijing, PR China

10. Yunnan Institute of Digestive Diseases, Kunming, PR China

11. Department of Gastroenterology, The First Affiliated Hospital of Kunming Medical University, Kunming, PR China

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.

Funder

the Doctoral Scientific Research Foundation of the First Affiliated Hospital of Kunming Medical University

Publisher

Microbiology Society

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