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Investigation of the association between clinical outcome and the cag pathogenicity-island and other virulence genes of Helicobacter pylori isolates from patients with dyspepsia in Eastern Turkey

机译:土耳其东部消化不良患者幽门螺杆菌分离株的临床结果与cag致病岛和其他毒力基因之间的关联研究

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摘要

The aims of our work were to determine the presence of the cag pathogenicity-island (cag PAI) and other virulence genes of Helicobacter pylori recovered from patients with gastritis and peptic ulcer, and to investigate the correlation of these virulence genes with clinical outcome. The presence of the cagA, the promoter regions of cagA, cagE, cagT, and the left end of cag-PAI (LEC), cag right junction (cagRJ), the plasticity region open reading frames (ORFs), vacA and oipA genes among 69 H. pylori isolates were determined by polymerase chain reaction. Intact cag PAI was detected in only one (1.4%) isolate. The cagA gene was identified in 52.1% and 76.2% of isolates from patients with dyspepsia (gastritis and peptic ulcer), respectively. The plasticity region ORFs i.e. JHP912 and JHP931 were predominantly detected in isolates from peptic ulcer. Less than 25% of the isolates carried other ORFs. Types I, II and III were the most commonly found among the isolates. None of the isolates possessed type Ib, 1c, IIIb, IV and V motifs. The most commonly vacA genotypes were s1am1a and s1m2 in isolates with peptic ulcer and gastritis, respectively. The results confirmed that the prevalence of oipA (Hp0638) gene was 75% and 85.7% in patients with gastritis and peptic ulcer, respectively. Furthermore, vacA s1am1a positivity was significantly related to peptic ulcer (p < 0.05).
机译:我们的工作目的是确定从胃炎和消化性溃疡患者中回收的cag致病岛(cag PAI)和其他毒力基因的存在,并研究这些毒力基因与临床结果的相关性。 cagA,cagA,cagE,cagT的启动子区域以及cag-PAI的左端(LEC),cag右连接点(cagRJ),可塑性区域开放阅读框(ORF),vacA和oipA基因的存在通过聚合酶链反应确定了69株幽门螺杆菌。仅在一种(1.4%)分离物中检测到完整的cag PAI。在消化不良患者(胃炎和消化性溃疡)分离株中分别鉴定出cagA基因52.1%和76.2%。主要在来自消化性溃疡的分离物中检测到可塑性区域ORF,即JHP912和JHP931。不到25%的分离株携带其他ORF。 I,II和III型是分离株中最常见的。分离株均不具有Ib,1c,IIIb,IV和V型基序。在患有消化性溃疡和胃炎的分离株中,最常见的vacA基因型分别是s1am1a和s1m2。结果证实,胃炎和消化性溃疡患者的oipA(Hp0638)基因患病率分别为75%和85.7%。此外, vacA s1am1a阳性与消化性溃疡显着相关(p <0.05)。

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