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cagPAI 是完整且功能正常的,但在马来西亚和新加坡的幽门螺杆菌分离株中,HP0521 有很大的差异。

The cag PAI is intact and functional but HP0521 varies significantly in Helicobacter pylori isolates from Malaysia and Singapore.

机构信息

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW, Australia.

出版信息

Eur J Clin Microbiol Infect Dis. 2010 Apr;29(4):439-51. doi: 10.1007/s10096-010-0881-7. Epub 2010 Feb 16.

Abstract

Helicobacter pylori-related disease is at least partially attributable to the genotype of the infecting strain, particularly the presence of specific virulence factors. We investigated the prevalence of a novel combination of H. pylori virulence factors, including the cag pathogenicity island (PAI), and their association with severe disease in isolates from the three major ethnicities in Malaysia and Singapore, and evaluated whether the cag PAI was intact and functional in vitro. Polymerase chain reaction (PCR) was used to detect dupA, cagA, cagE, cagT, cagL and babA, and to type vacA, the EPIYA motifs, HP0521 alleles and oipA ON status in 159 H. pylori clinical isolates. Twenty-two strains were investigated for IL-8 induction and CagA translocation in vitro. The prevalence of cagA, cagE, cagL, cagT, babA, oipA ON and vacA s1 and i1 was >85%, irrespective of the disease state or ethnicity. The prevalence of dupA and the predominant HP0521 allele and EPIYA motif varied significantly with ethnicity (p < 0.05). A high prevalence of an intact cag PAI was found in all ethnic groups; however, no association was observed between any virulence factor and disease state. The novel association between the HP0521 alleles, EPIYA motifs and host ethnicity indicates that further studies to determine the function of this gene are important.

摘要

幽门螺杆菌相关疾病至少部分归因于感染菌株的基因型,特别是特定毒力因子的存在。我们研究了新型幽门螺杆菌毒力因子组合(包括 cag 致病岛(PAI))在马来西亚和新加坡三大种族分离株中的流行情况及其与严重疾病的关联,并评估了 cag PAI 在体外是否完整且具有功能。聚合酶链反应(PCR)用于检测 dupA、cagA、cagE、cagT、cagL 和 babA,并对 vacA、EPIYA 基序、HP0521 等位基因和 oipA ON 状态进行分型在 159 株幽门螺杆菌临床分离株中。对 22 株菌株进行了体外 IL-8 诱导和 CagA 易位研究。cagA、cagE、cagL、cagT、babA、oipA ON 和 vacA s1 和 i1 的流行率>85%,与疾病状态或种族无关。dupA 的流行率和主要的 HP0521 等位基因和 EPIYA 基序因种族而异(p<0.05)。所有种族都发现 cag PAI 高度完整;然而,没有观察到任何毒力因子与疾病状态之间存在关联。HP0521 等位基因、EPIYA 基序和宿主种族之间的新关联表明,进一步研究确定该基因的功能很重要。

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