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Distribution of Helicobacter pylori virulence markers in patients with gastroduodenal diseases in a region at high risk of gastric cancer.在胃癌高发地区,胃十二指肠疾病患者中幽门螺杆菌毒力标志物的分布。
Microb Pathog. 2013 Jun-Jul;59-60:13-8. doi: 10.1016/j.micpath.2013.04.001. Epub 2013 Apr 9.
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Helicobacter pylori virulence genes detected by string PCR in children from an urban community in northeastern Brazil.巴西东北部一城市社区儿童中通过串珠聚合酶链反应检测到的幽门螺杆菌毒力基因。
J Clin Microbiol. 2013 Mar;51(3):988-9. doi: 10.1128/JCM.02583-12. Epub 2012 Dec 19.
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The relationship between H. pylori virulence genotypes and gastric diseases.幽门螺杆菌毒力基因型与胃部疾病的关系。
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Pathogenesis of Helicobacter pylori-Related Gastroduodenal Diseases from Molecular Epidemiological Studies.从分子流行病学研究看幽门螺杆菌相关胃十二指肠疾病的发病机制。
Gastroenterol Res Pract. 2012;2012:371503. doi: 10.1155/2012/371503. Epub 2012 Jul 5.
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Association between cagA and vacA genotypes and pathogenesis in a Helicobacter pylori infected population from South-eastern Sweden.在瑞典东南部的一个幽门螺杆菌感染人群中,cagA 和 vacA 基因型与发病机制之间的关系。
BMC Microbiol. 2012 Jul 2;12:129. doi: 10.1186/1471-2180-12-129.
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Infection with Helicobacter pylori strains lacking dupA is associated with an increased risk of gastric ulcer and gastric cancer development.感染缺乏 dupA 的幽门螺杆菌菌株与胃溃疡和胃癌发展的风险增加有关。
J Med Microbiol. 2012 Jan;61(Pt 1):23-30. doi: 10.1099/jmm.0.027052-0. Epub 2011 Sep 8.
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dupA polymorphisms and risk of Helicobacter pylori-associated diseases.dupA 多态性与幽门螺杆菌相关疾病的风险。
Int J Med Microbiol. 2011 Mar;301(3):225-8. doi: 10.1016/j.ijmm.2010.08.019. Epub 2010 Nov 2.
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Mechanisms of disease: Helicobacter pylori virulence factors.发病机制:幽门螺杆菌毒力因子。
Nat Rev Gastroenterol Hepatol. 2010 Nov;7(11):629-41. doi: 10.1038/nrgastro.2010.154. Epub 2010 Oct 12.
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Helicobacter pylori dupA and gastric acid secretion are negatively associated with gastric cancer development.幽门螺杆菌 dupA 与胃酸分泌与胃癌发展呈负相关。
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巴西患者中幽门螺杆菌毒力标记物 dupA、cagA 和 vacA 之间的关联。

Association among H. pylori virulence markers dupA, cagA and vacA in Brazilian patients.

机构信息

Sacred Heart University, Bauru, São Paulo State, Brazil.

出版信息

J Venom Anim Toxins Incl Trop Dis. 2014 Jan 23;20(1):1. doi: 10.1186/1678-9199-20-1.

DOI:10.1186/1678-9199-20-1
PMID:24456629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3922733/
Abstract

BACKGROUND

Only a few Helicobacter pylori-infected individuals develop severe gastric diseases and virulence factors of H. pylori appear to be involved in such clinical outcomes. Duodenal ulcer promoting gene A (dupA) is a novel virulence factor of Helicobacter pylori that is associated with duodenal ulcer development and reduced risk for gastric carcinoma in some populations. The aims of the present study were to determine the presence of dupA gene and evaluate the association among dupA and other virulence factors including cagA and vacA in Brazilian patients. Gastric biopsies were obtained from 205 dyspeptic patients (100 children and 105 adults). DNA was extracted and analyzed for the presence of H. pylori and its virulence factors using the polymerase chain reaction method.

RESULTS

Patients with gastritis tested positive for H. pylori more frequently. The dupA gene was detected in 41.5% of them (85/205); cagA gene was found in 98 isolates (47.8%) and vacA genotype s1/m1 in 50.2%, s1/m2 in 8.3%, s2/m2 in 36.6%, s2/m1 in 0.5% and s1/s2/m1/m2 in 4.4%. We also verified a significant association between cagA and dupA genes [p = 0.0003, relative risk (RR) 1.73 and confidence interval [CI] = 1.3-2.3]. The genotypes s1/m1 were also associated with dupA gene (p = 0.0001, RR: 1.72 and CI: 1.3-2.2). The same associations were found when analyzing pediatric and adult groups of patients individually.

CONCLUSION

Ours results suggest that dupA is highly frequent in Brazilian patients and is associated with cagA gene and vacA s1/m1 genotype, and it may be considered an important virulence factor in the development of gastric diseases in adults or children.

摘要

背景

只有少数幽门螺杆菌感染个体发展为严重的胃部疾病,而幽门螺杆菌的毒力因子似乎与这些临床结局有关。十二指肠溃疡促进基因 A(dupA)是一种新型的幽门螺杆菌毒力因子,与某些人群的十二指肠溃疡发展和胃癌风险降低有关。本研究的目的是确定 dupA 基因的存在,并评估其与其他毒力因子(包括 cagA 和 vacA)之间的关联在巴西患者中的情况。从 205 例消化不良患者(100 例儿童和 105 例成人)中获取胃活检组织。使用聚合酶链反应方法提取和分析 DNA,以检测 H. pylori 及其毒力因子的存在。

结果

患有胃炎的患者 H. pylori 检测呈阳性的频率更高。在他们中,dupA 基因的检出率为 41.5%(85/205);cagA 基因在 98 株菌中被发现(47.8%),vacA 基因型 s1/m1 为 50.2%,s1/m2 为 8.3%,s2/m2 为 36.6%,s2/m1 为 0.5%,s1/s2/m1/m2 为 4.4%。我们还验证了 cagA 和 dupA 基因之间存在显著关联[p=0.0003,相对风险(RR)1.73,置信区间(CI)=1.3-2.3]。s1/m1 基因型也与 dupA 基因相关(p=0.0001,RR:1.72,CI:1.3-2.2)。在分别分析儿科和成人患者组时,也发现了相同的关联。

结论

我们的结果表明,dupA 在巴西患者中高度频繁,与 cagA 基因和 vacA s1/m1 基因型相关,它可能是成人或儿童胃部疾病发展的一个重要毒力因子。