Laboratory of Microbiology of Institute Aggeu Magalhães (IAM), Foundation Oswaldo Cruz, Av. Prof. Moraes Rego, 1235, Cidade Universitária, Recife, PE, Brazil.
Department of Internal Medicine, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.
Braz J Microbiol. 2024 Sep;55(3):2631-2641. doi: 10.1007/s42770-024-01380-4. Epub 2024 May 28.
Helicobacter pylori is a major cause of gastrointestinal disorders such as chronic gastritis, peptic ulcers, mucosa-associated lymphoid tissue (MALT) lymphoma, and gastric cancer. It is estimated that around half of the world's population is infected with this pathogen, with underdeveloped countries reporting the highest frequencies. The genes cagA, cagM, vacA, and oipA are some of the most important virulence factors of H. pylori; however, there are no recent studies from Recife-PE demonstrating their frequency, and their relationship with severe gastric modifications. This work aims to use qualitative PCR to detect the virulence genes cagA, cagM, vacA, and oipA in H. pylori isolates obtained from patients in a public hospital in Recife (PE). We collected samples from the stomach's body and antrum of 147 patients, from which 71 (48%) tested positive for H. pylori. Among positive samples, the most frequently infected gender was female (44/71, 62%), and the most frequently infected age group was those above the age of 46 (31/71, 44%). Histological examination of H. pylori-positive samples revealed alterations other than chronic gastritis, including metaplasia and atrophy. The frequency of cagA, cagM, and oipA genes were identified in 84%, 56%, and 69% of the samples tested, respectively, as well as the vacA-s1m1 allelic combination (77%). However, there was no statistically significant variation in the occurrence of these genes, therefore they cannot be considered unique markers of severity in our setting. New research with larger samples and investigations of other genetic markers can aid uncover local risk factors and lead to a better understanding of H. pylori's pathogenesis.
幽门螺杆菌是导致胃肠道疾病的主要原因之一,如慢性胃炎、消化性溃疡、黏膜相关淋巴组织(MALT)淋巴瘤和胃癌。据估计,全球约有一半的人口感染了这种病原体,欠发达国家的感染率最高。cagA、cagM、vacA 和 oipA 等基因是幽门螺杆菌最重要的毒力因子之一;然而,最近来自累西腓-PE 的研究并未显示这些基因的频率及其与严重胃改变的关系。本研究旨在使用定性聚合酶链反应(PCR)检测从累西腓(PE)一家公立医院的患者中分离的幽门螺杆菌分离株中的毒力基因 cagA、cagM、vacA 和 oipA。我们从 147 名患者的胃体和胃窦部位采集了样本,其中 71 名(48%)检测出幽门螺杆菌阳性。在阳性样本中,感染的女性比例最高(44/71,62%),感染的最常见年龄组为 46 岁以上(31/71,44%)。对幽门螺杆菌阳性样本的组织学检查显示,除了慢性胃炎外,还存在化生和萎缩等改变。在检测的样本中,cagA、cagM 和 oipA 基因的频率分别为 84%、56%和 69%,以及 vacA-s1m1 等位基因组合(77%)。然而,这些基因的发生没有统计学上的显著差异,因此它们不能被认为是我们研究环境中严重程度的独特标志物。需要进行具有更大样本量的新研究,并对其他遗传标志物进行调查,以帮助揭示当地的风险因素,并深入了解幽门螺杆菌的发病机制。