首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >CagA C-terminal variations in Helicobacter pylori strains from Colombian patients with gastric precancerous lesions.
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CagA C-terminal variations in Helicobacter pylori strains from Colombian patients with gastric precancerous lesions.

机译:CAGA C末端胃癌患者胃癌患者幽门螺杆菌菌株的变异。

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摘要

The C-terminus of the Helicobacter pylori CagA protein is polymorphic, bearing different EPIYA sequences (EPIYA-A, B, C or D), and one or more CagA multimerization (CM) motifs. The number of EPIYA-C motifs is associated with precancerous lesions and gastric cancer (GC). The relationship between EPIYA, CM motifs and gastric lesions was examined in H. pylori-infected Colombian patients from areas of high and low risk for GC. Genomic DNA was extracted from H. pylori strains cultured from gastric biopsies from 80 adults with dyspeptic symptoms. Sixty-seven (83.8%) of 80 strains were cagA positive. The 3' region of cagA was sequenced, and EPIYA and CM motifs were identified. CagA proteins contained one (64.2%), two (34.3%) or three EPIYA-C motifs (1.5%), all with Western type CagA-specific sequences. Strains with one EPIYA-C motif were associated with less severe gastric lesions (non-atrophic and multifocal atrophic gastritis), whereas strains with multiple EPIYA-C motifs were associated with more severe lesions (intestinal metaplasia and dysplasia) (p <0.001). In 54 strains, the CM motifs were identical to those common in Western strains. Thirteen strains from the low-risk area contained two different CM motifs: one of Western type located within the EPIYA-C segment and another following the EPIYA-C segment and resembling the CM motif found in East Asian strains. These strains induced significantly shorter projections in AGS cells and an attenuated reduction in levels of CagA upon immunodepletion of SHP-2 than strains possessing Western/Western motifs. This novel finding may partially explain the difference in GC incidence in these populations.
机译:幽门螺杆菌Caga蛋白的C-末端是多态性的,轴承不同的外部序列(Epiya-A,B,C或D)和一个或多个CAGA多聚化(CM)基序。 Epiya-C主题的数量与癌前病变和胃癌(GC)有关。在H.幽门螺杆菌感染的哥伦比亚患者中检查了EPIYA,CM图谱和胃病变之间的关系,从GC的高风险和低风险。从80名成人培养的胃活组织检查培养的H.幽门螺杆菌菌株中提取基因组DNA。六十七(83.8%)的80株菌株是Caga阳性。 CAGA的3'区域被测序,鉴定了ePIYA和CM基序。 Caga蛋白含有一种(64.2%),两种(34.3%)或三个epiya-c主题(1.5%),全部包含西方类型的Caga特异性序列。具有一种Epiya-C基序的菌株与较小的胃病病变(非萎缩和多灶性萎缩性胃炎)有关,而具有多种EPIYA-C基序的菌株与更严重的病变(肠道脑癌和发育不良)有关(P <0.001)。在54个菌株中,CM基序与西方菌株中常见的基序相同。来自低风险区域的十三个菌株包含两种不同的CM图案:西方类型之一位于Epiya-C段内,另一种在Epiya-C段和类似于东亚菌株中发现的CM主题。这些菌株在AGS细胞中诱导显着较短的突起,并且在SHP-2的免疫刻度上的CAGA水平的减毒降低而不是具有西方/西方基序的菌株。这部小说发现可能部分解释这些人群中GC发病率的差异。

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