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Heterogeneity in the Activity of Mexican Helicobacter pylori Strains in Gastric Epithelial Cells and Its Association with Diversity in the cagA Gene

机译:墨西哥幽门螺杆菌菌株在胃上皮细胞活性中的异质性及其与cagA基因多样性的关系

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摘要

Helicobacter pylori CagA is translocated into gastric epithelial cells by a type IV secretion system and interacts with the Src homology 2 phosphatase, altering cell morphology. Multiple EPIYA motifs in CagA are associated with increased activity in cells and with gastric cancer. The aim of this work was to study the heterogeneity in activity in cells of multiple H. pylori single colonies isolated from a single patient and its association with polymorphism in cagA. The presence of cagA, cagE, cagT, and cag10 was studied with 318 H. pylori isolates from the antra and corpora of 18 patients. AGS gastric epithelial cells were infected with 75 isolates, and interleukin-8 (IL-8) secretion, cytoskeletal changes, CagA translocation, and tyrosine phosphorylation were measured. The cagA 3′-variable region was sequenced for 30 isolates to determine the number and types of EPIYA motifs. Isolates from an individual stomach were usually genetically related and had quantitatively similar phenotypic effects on cells (IL-8 induction and cytoskeletal changes). However, strains from different patients with similar CagA EPIYA motif patterns varied widely in these phenotypes. Among isolates with an EPIYA-ABC pattern, the phenotype was variable: IL-8 induction ranged from 200 to 1,200 pg/ml, and morphological changes occurred in 20 to 70% of cells. In several cases, cagA sequence diversity appeared to explain the lack of CagA activity, as isolates with an EPIYA-ACC pattern or a modified B motif had reduced cell activity. cag pathogenicity island-positive H. pylori isolates displayed a high level of heterogeneity in the capacity to induce IL-8 secretion and morphological changes; an absent or modified B motif was associated with low activity.
机译:幽门螺杆菌CagA通过IV型分泌系统转移到胃上皮细胞中,并与Src同源2磷酸酶相互作用,从而改变细胞形态。 CagA中的多个EPIYA基序与细胞和胃癌的活性增加有关。这项工作的目的是研究从单个患者中分离出的多个幽门螺杆菌单个菌落在细胞中活性的异质性及其与cagA多态性的关系。用来自18例患者的肛门和体的318幽门螺杆菌分离株研究了cagA,cagE,cagT和cag10的存在。将AGS胃上皮细胞感染75株分离株,并测量白细胞介素8(IL-8)分泌,细胞骨架变化,CagA易位和酪氨酸磷酸化。对30个分离株的cagA 3'可变区进行测序,以确定EPIYA基序的数量和类型。通常,从单个胃中分离出的分离物具有遗传相关性,并且对细胞具有定量相似的表型效应(IL-8诱导和细胞骨架变化)。但是,来自不同患者的具有相似CagA EPIYA基序模式的菌株在这些表型中差异很大。在具有EPIYA-ABC模式的分离株中,表型是可变的:IL-8诱导的范围为200至1,200 pg / ml,形态变化发生在20%至70%的细胞中。在某些情况下,cagA序列的多样性似乎可以解释CagA活性的缺乏,因为具有EPIYA-ACC模式或修饰的B基序的分离株的细胞活性降低。 cag致病性岛阳性幽门螺杆菌分离物在诱导IL-8分泌和形态变化的能力上显示出高度异质性;缺少或修饰的B基序与低活性相关。

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