首页> 外文期刊>Chinese Medical Journal >Dominant cagA/vacA genotypes and coinfection frequency of H. pylori in peptic ulcer or chronic gastritis patients in Zhejiang Province and correlations among different genotypes, coinfection and severity of the diseases
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Dominant cagA/vacA genotypes and coinfection frequency of H. pylori in peptic ulcer or chronic gastritis patients in Zhejiang Province and correlations among different genotypes, coinfection and severity of the diseases

机译:浙江省消化性溃疡或慢性胃炎患者幽门螺杆菌主要cagA / vacA基因型和合并感染频率以及不同基因型,合并感染和疾病严重程度的相关性

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Background Almost half of the world's population suffer from the Helicobacter pylori (H. pylori) infection , but only some individuals develop gastric diseases with clinical symptoms. One reason for the phenomenon may be the different pathogenicity of infected H. pylori strains. The presence of cytotoxin-associated gene A (cagA) and expression of vacuolating cytotoxin activity encoded by vacuolating cytotoxin gene A (vacA) are considered the two major virulent markers of H. pylori. The aim of this study was to detect dominant cagA/vacA genolypes and coinfection frequency of H. pylori in patients with peptic ulceration (PU) or chronic gastritis (CG), and to determine correlations among different cagA/vacA genotypes, coinfection and severity of the diseases. Methods For each of 139 patients in Zhejiang Province who had been diagnosed as PU or CG based on clinical symptoms and gastroscopy, two gastric biopsy specimens (one from antrum and the other from corpus) for H. pylori isolation were taken by two different disinfected biopsy forceps. One hundred and fifty-six H. pylori strains were isolated from both the antrum and corpus biopsy specimens of 78 patients (36 PU and 42 CG). PCRs were performed to detect cagA genes, and signal (s) and middle (m) regions of vacA genes in the H. pylori isolates. The amplified fragments of dominant vacA gene s and m subtypes from representative H. pylori isolates were sequenced after TA cloning. Dominant cagA/vacA genotypes of the H. pylori isolates, coinfection frequency and correlations among the different genotypes, coinfection and severity of the diseases were determined. Results Of the H. pylori strains isolated from the antrum specimens, 96.2% were cagA gene positive, as were 97.4% of the H. pylori strains isolated from the corpus specimens. Only one s region subtype (sla) and four m region subtypes m1, m2, m1b and m1b-m2 of vacA gene were found. The proportions of vacA gene subtypes s1a/m1, s1a/m2, s1a/m1b and s1a/m1b-m2 in the 83 strains isolated from the antrum specimens were 7.2%, 61.5%, 30.1% and 1.2%, respectively, while those in the other 84 strains isolated from the corpus specimens were 9.5%, 58.3%, 28.6% and 3.6%, respectively. s1a/m2 (58.3% vs 30.1%, χ~2 = 13.47, P < 0.01 ) and then s1a/m1b (28.6% vs 9.5%, χ~2 = 9. 88, P < 0. 01) were the dominant vacA gene subtypes in the H. pylori isolates. The dominant H. pylori genotype was cagA + s1a/m2 (59.0% from antrum specimens and 57.1% from corpus specimens), and followed by cagA + s1a/m1b (28.9% from antrum specimens and 27.4% from corpus specimens). Sixteen of 78 patients (20.5%) were infected with two or three H. pylori strains with different genotypes. However, no statistically significant differences among cagA occurrence, the different vacA subtypes and PU or CG could be found (each P > 0.05). Similarities of the nucleotide sequences from vacA gene s region PCR products of six isolates and from vacA gene mregion PCR products of four isolates were 93.2% to 98.3% and 93.8% to 97.6%, respectively, compared to the reported corresponding sequences. Conclusions The dominant genotypes of H. pylori in PU or CG patients in Zhejiang area may be cagA + s1a/m2 and cagA + s1a/m1b. Numerous coinfections with different H, pylori strains in PU or CG patients indicate diversity of the infected H, pylori origins, s and m regions of vacA gene from different H. pylori isolates show high nucleotide sequence similarities.
机译:背景技术世界上有将近一半的人口患有幽门螺杆菌(H. pylori)感染,但只有一些人发展出具有临床症状的胃病。造成这种现象的原因之一可能是感染的幽门螺杆菌菌株的致病性不同。细胞毒素相关基因A(cagA)的存在和空泡细胞毒素基因A(vacA)编码的空泡细胞毒素活性的表达被认为是幽门螺杆菌的两个主要毒性标记。这项研究的目的是检测消化性溃疡(PU)或慢性胃炎(CG)患者的主要cagA / vacA基因型和幽门螺杆菌的合并感染频率,并确定不同cagA / vacA基因型,合并感染和严重程度之间的相关性疾病。方法对浙江省139例经临床症状和胃镜检查诊断为PU或CG的患者,分别进行两次不同的消毒活检,取两个胃活检标本(一个来自胃窦,另一个来自胃体)。钳子。从78例患者(36 PU和42 CG)的胃窦和尸体活检标本中分离出156株幽门螺杆菌。进行PCR以检测幽门螺杆菌分离物中的cagA基因以及vacA基因的信号区域和中间区域。 TA克隆后,对来自代表性幽门螺杆菌分离株的显性vacA基因s和m亚型的扩增片段进行测序。确定了幽门螺杆菌分离株的主要cagA / vacA基因型,合并感染频率以及不同基因型之间的相关性,合并感染和疾病的严重程度。结果从胃窦标本分离出的幽门螺杆菌菌株中,cagA基因阳性率为96.2%,从尸体标本分离出的幽门螺杆菌菌株为97.4%。 vacA基因仅发现一个s区亚型(sla)和四个m区亚型m1,m2,m1b和m1b-m2。从胃标本中分离出的83个菌株中vacA基因亚型s1a / m1,s1a / m2,s1a / m1b和s1a / m1b-m2的比例分别为7.2%,61.5%,30.1%和1.2%。从尸体标本中分离出的其他84个菌株分别为9.5%,58.3%,28.6%和3.6%。 s1a / m2(58.3%vs 30.1%,χ〜2 = 13.47,P <0.01)然后是s1a / m1b(28.6%vs 9.5%,χ〜2 = 9. 88,P <0. 01)是主导的vacA。幽门螺杆菌分离物中的基因亚型。幽门螺杆菌的主要基因型是cagA + s1a / m2(胃标本占59.0%,语料库样本占57.1%),其次是cagA + s1a / m1b(胃窦标本占28.9%,尸体标本占27.4%)。 78名患者中有16名(20.5%)感染了两种或三种不同基因型的幽门螺杆菌。但是,在cagA发生,不同的vacA亚型和PU或CG之间没有统计学上的显着差异(每个P> 0.05)。与报道的相应序列相比,来自六个分离株的vacA基因的区域PCR产物和来自四个分离株的vacA基因的m区PCR产物的核苷酸序列的相似性分别为93.2%至98.3%和93.8%至97.6%。结论浙江地区PU或CG患者中幽门螺杆菌的主要基因型可能是cagA + s1a / m2和cagA + s1a / m1b。在PU或CG患者中使用不同的H. pylori菌株进行的许多合并感染表明,来自不同H. pylori分离株的vacA基因的被感染H,pylori起源,s和m区具有多样性。

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