Instituto de Patologia Tropical e Saúde Pública, Núcleo de Estudo da Helicobacter pylori, Departamento de Biociências e Tecnologia, Universidade Federal de Goiás, Leste Universitário, Goiânia, GO, Brazil.
Departamento de Medicina, Faculdade de Ciências Médicas, Farmacêuticas e Biomédicas, Universidade Católica de Goiás, Goiânia, GO, Brazil.
Braz J Microbiol. 2021 Dec;52(4):1921-1927. doi: 10.1007/s42770-021-00553-9. Epub 2021 Jul 13.
Helicobacter pylori is the etiological agent of chronic gastritis, peptic ulcer, and gastric cancer. The duodenal ulcer-promoting gene dupA, which is located in the plasticity region of the H. pylori genome, is homologous to the virB gene which encodes a type IV secretion protein in Agrobacterium tumefaciens. Studies have shown associations between H. pylori dupA-positive strains and gastroduodenal diseases. However, whether dupA acts as a risk factor or protective factor in these diseases remains unclear. Therefore, in this study, we aimed to verify the presence of the dupA gene in infectious H. pylori strains in the Brazilian mid-west and to investigate its association with the clinical outcomes of patients with dyspepsia. Additionally, the phylogenetic origin of the strains was determined. Gastric biopsies from 117 patients with dyspepsia were analyzed using histological and molecular techniques. The hpx gene (16S rRNA) was used to screen for H. pylori infection, and positive samples were then subjected to dupA gene detection and sequencing. The estimated prevalence of H. pylori infection was 64.1%, with the dupA gene being detected in a high proportion of infectious strains (70.7%). Furthermore, a risk analysis revealed that for women, a dupA-positive H. pylori infection increased the chance of developing gastritis by twofold. The partial dupA sequences from isolated infectious strains in this work are similar to those of strains isolated in westerns countries. This study provides useful insights for understanding the role of the H. pylori dupA gene in disease development.
幽门螺杆菌是慢性胃炎、消化性溃疡和胃癌的病因。位于幽门螺杆菌基因组可塑性区域的十二指肠溃疡促进基因 dupA 与编码根癌农杆菌 IV 型分泌蛋白的 virB 基因同源。研究表明,幽门螺杆菌 dupA 阳性菌株与胃十二指肠疾病之间存在关联。然而,dupA 在这些疾病中是作为危险因素还是保护因素尚不清楚。因此,本研究旨在验证巴西中西部传染性幽门螺杆菌菌株中是否存在 dupA 基因,并研究其与消化不良患者临床结局的关系。此外,还确定了菌株的系统发育起源。采用组织学和分子技术分析了 117 例消化不良患者的胃活检标本。用 hpx 基因(16S rRNA)筛选幽门螺杆菌感染,对阳性样本进行 dupA 基因检测和测序。估计幽门螺杆菌感染的患病率为 64.1%,传染性菌株中检测到高比例的 dupA 基因(70.7%)。此外,风险分析表明,对于女性而言,dupA 阳性的幽门螺杆菌感染使胃炎发病的几率增加了两倍。本研究中从分离的传染性菌株中获得的部分 dupA 序列与从西方国家分离的菌株相似。这项研究为理解幽门螺杆菌 dupA 基因在疾病发展中的作用提供了有用的信息。