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使用高灵敏度实时聚合酶链反应作为一种新的诊断工具,对胃活检组织中的幽门螺杆菌和cagA基因型进行鉴定。

Identification of Helicobacter pylori and the cagA genotype in gastric biopsies using highly sensitive real-time PCR as a new diagnostic tool.

作者信息

Yamazaki Shiho, Kato Shunji, Matsukura Norio, Ohtani Masahiro, Ito Yoshiyuki, Suto Hiroyuki, Yamazaki Yukinao, Yamakawa Akiyo, Tokudome Shinkan, Higashi Hideaki, Hatakeyama Masanori, Azuma Takeshi

机构信息

Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka-cho, Yoshida-gun, Fukui 910-1193, Japan.

出版信息

FEMS Immunol Med Microbiol. 2005 Jun 1;44(3):261-8. doi: 10.1016/j.femsim.2004.12.011.

Abstract

The CagA protein is one of the virulence factors of Helicobacter pylori, and two major subtypes of CagA have been observed, the Western and East Asian type. CagA is injected from the bacteria into gastric epithelial cells, undergoes tyrosine phosphorylation, and binds to Src homology 2 domain-containing protein-tyrosine phosphatase SHP-2. The East Asian type CagA binds to SHP-2 more strongly than the Western type CagA. Here, we tried to distinguish the CagA type by highly sensitive real-time PCR with the objective of establishing a system to detect H. pylori and CagA subtypes from gastric biopsies. We designed primers and probe sets for Western or East Asian-cagA at Western-specific or East Asian-specific sequence regions, respectively, and H. pylori 16S rRNA. We could detect the H. pylori 16S rRNA gene, Western and East Asian-cagA gene from DNA of gastric biopsies. The sensitivity and specificity for H. pylori infection was 100% in this system. In Thai patients, 87.8% (36/41) were cagA-positive; 26.8% (11/41) were Western-cagA positive and 53.7% (22/41) were East Asian-cagA positive, while 7.3% (3/41) reacted with both types of cagA. These results suggest that this real-time PCR system provides a highly sensitive assessment of CagA type as a new diagnostic tool for the pathogenicity of H. pylori infection.

摘要

细胞毒素相关基因A(CagA)蛋白是幽门螺杆菌的毒力因子之一,已观察到CagA有两种主要亚型,即西方型和东亚型。CagA从细菌注入胃上皮细胞,发生酪氨酸磷酸化,并与含Src同源2结构域的蛋白酪氨酸磷酸酶SHP-2结合。东亚型CagA比西方型CagA与SHP-2的结合更强。在此,我们试图通过高灵敏度实时聚合酶链反应(PCR)来区分CagA类型,目的是建立一种从胃活检组织中检测幽门螺杆菌及CagA亚型的系统。我们分别针对西方型或东亚型CagA的西方特异性或东亚特异性序列区域以及幽门螺杆菌16S核糖体RNA(rRNA)设计了引物和探针组。我们能够从胃活检组织的DNA中检测到幽门螺杆菌16S rRNA基因、西方型和东亚型CagA基因。该系统对幽门螺杆菌感染的灵敏度和特异性均为100%。在泰国患者中,87.8%(36/41)的患者CagA呈阳性;26.8%(11/41)为西方型CagA阳性,53.7%(22/41)为东亚型CagA阳性,而7.3%(3/41)的患者对两种类型的CagA均有反应。这些结果表明,这种实时PCR系统作为一种用于评估幽门螺杆菌感染致病性的新诊断工具,能够对CagA类型进行高度灵敏的评估。

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