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幽门螺杆菌侵袭能力与胃十二指肠疾病之间关系的分析

Analysis of the relationship between invasive capability of Helicobacter pylori and gastroduodenal diseases.

作者信息

Zhang Xiaoyan, Zhang Jie, Lin Yunbin, Xu Kai, Li Neng, Chen Hao, She Feifei

机构信息

Key Laboratory of Ministry of Education for Gastrointestinal Cancer, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350108, PR China.

出版信息

J Med Microbiol. 2015 May;64(Pt 5):498-506. doi: 10.1099/jmm.0.000049. Epub 2015 Mar 9.

Abstract

Helicobacter pylori (H. pylori) may enter into host cells, maybe as a facultative intracellular pathogen. This study aims to reveal the roles of internalized H. pylori in the bacterial pathopoiesis. Transmission electron microscopy was used to observe the invasion of H. pylori. Invasion rates of H. pylori (two standard strains and 43 clinical strains) were examined by gentamicin invasion assay. The cagA, cagE and vacA genes of H. pylori were detected by PCR. The cagA 3'region (cagA-EPIYA) of each strain was sequenced. The secretion of IL-8 from AGS cells and activity of NF-κB induced by intracellular H. pylori were tested by ELISA and the dual-luciferase reporter assay system, respectively. It was found that H. pylori could adhere to and invade AGS cells, then continue to survive and multiply in the cytoplasm. The average invasion rate of H. pylori gastric cancer plants and that of ulcer plants were both higher than that of gastritis plants (P ≈ 0.0001). In the clinical strains, cagA, vacA and cagE were all positive; cagA-EPIYA genotypes included ABD 90.7% (39/43) and ABBD 9.3% (4/43), all without comparability. Notably, the average invasion rate of H. pylori vacA s1c-i1-m1b plants was higher than that of vacA s1c-i1-m2 plants (P=0.0445). In addition, the intracellular H. pylori all could induce IL-8 secretion, which was decreased after cells were pretreated with anti-β1-integrin antibody or SN-50 (an NF-κB inhibitor). The intracellular H. pylori all activated NF-κB, which would be inhibited after cells were pretreated with anti-β1-integrin antibody. These results demonstrate that H. pylori invasive ability and disease severity have a positive correlation, and this intension of invasive ability is associated with the vacA mid-region, not with cagA, cagA-EPIYA or cagE. It is possible that cagA and cagE are essential for the bacterial invasion. Internalized H. pylori can activate NF-κB signal pathway and induce IL-8 secretion, which suggests that H. pylori invasion may be an important strategy to play a role in the development of H. pylori associated diseases.

摘要

幽门螺杆菌(H. pylori)可能作为兼性胞内病原体进入宿主细胞。本研究旨在揭示内化的幽门螺杆菌在细菌致病过程中的作用。采用透射电子显微镜观察幽门螺杆菌的侵袭情况。通过庆大霉素侵袭试验检测幽门螺杆菌(2株标准菌株和43株临床菌株)的侵袭率。采用聚合酶链反应(PCR)检测幽门螺杆菌的cagA、cagE和vacA基因。对各菌株的cagA 3'区域(cagA-EPIYA)进行测序。分别采用酶联免疫吸附测定(ELISA)和双荧光素酶报告基因检测系统检测AGS细胞中白细胞介素-8(IL-8)的分泌以及细胞内幽门螺杆菌诱导的核因子κB(NF-κB)活性。结果发现,幽门螺杆菌能够黏附并侵袭AGS细胞,然后在细胞质中继续存活和增殖。幽门螺杆菌在胃癌组织和溃疡组织中的平均侵袭率均高于胃炎组织(P≈0.0001)。在临床菌株中,cagA、vacA和cagE均为阳性;cagA-EPIYA基因型包括ABD型90.7%(39/43)和ABBD型9.3%(4/43),均无可比性。值得注意的是,幽门螺杆菌vacA s1c-i1-m1b型菌株的平均侵袭率高于vacA s1c-i1-m2型菌株(P=0.0445)。此外,细胞内幽门螺杆菌均能诱导IL-8分泌,在用抗β1整合素抗体或SN-50(一种NF-κB抑制剂)预处理细胞后,IL-8分泌减少。细胞内幽门螺杆菌均能激活NF-κB,在用抗β1整合素抗体预处理细胞后,NF-κB激活受到抑制。这些结果表明,幽门螺杆菌的侵袭能力与疾病严重程度呈正相关,且这种侵袭能力的强弱与vacA中间区域有关,而与cagA、cagA-EPIYA或cagE无关。cagA和cagE可能对细菌的侵袭至关重要。内化的幽门螺杆菌可激活NF-κB信号通路并诱导IL-8分泌,这表明幽门螺杆菌的侵袭可能是其在幽门螺杆菌相关疾病发生发展中发挥作用的重要策略。

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