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小肠结肠炎耶尔森菌O:9血清型O-多糖基因簇的特征及生物学作用

Characterization and biological role of the O-polysaccharide gene cluster of Yersinia enterocolitica serotype O:9.

作者信息

Skurnik Mikael, Biedzka-Sarek Marta, Lübeck Peter S, Blom Tea, Bengoechea José Antonio, Pérez-Gutiérrez Camino, Ahrens Peter, Hoorfar Jeffrey

机构信息

Department of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Finland.

出版信息

J Bacteriol. 2007 Oct;189(20):7244-53. doi: 10.1128/JB.00605-07. Epub 2007 Aug 10.

Abstract

Yersinia enterocolitica serotype O:9 is a gram-negative enteropathogen that infects animals and humans. The role of lipopolysaccharide (LPS) in Y. enterocolitica O:9 pathogenesis, however, remains unclear. The O:9 LPS consists of lipid A to which is linked the inner core oligosaccharide, serving as an attachment site for both the outer core (OC) hexasaccharide and the O-polysaccharide (OPS; a homopolymer of N-formylperosamine). In this work, we cloned the OPS gene cluster of O:9 and identified 12 genes organized into four operons upstream of the gnd gene. Ten genes were predicted to encode glycosyltransferases, the ATP-binding cassette polysaccharide translocators, or enzymes required for the biosynthesis of GDP-N-formylperosamine. The two remaining genes within the OPS gene cluster, galF and galU, were not ascribed a clear function in OPS biosynthesis; however, the latter gene appeared to be essential for O:9. The biological functions of O:9 OPS and OC were studied using isogenic mutants lacking one or both of these LPS parts. We showed that OPS and OC confer resistance to human complement and polymyxin B; the OPS effect on polymyxin B resistance could be observed only in the absence of OC.

摘要

小肠结肠炎耶尔森菌O:9血清型是一种感染动物和人类的革兰氏阴性肠道病原体。然而,脂多糖(LPS)在小肠结肠炎耶尔森菌O:9致病机制中的作用仍不清楚。O:9 LPS由脂质A组成,脂质A与内核寡糖相连,内核寡糖是外核(OC)六糖和O-多糖(OPS;N-甲酰过氧胺的同聚物)的附着位点。在这项研究中,我们克隆了O:9的OPS基因簇,并在gnd基因上游鉴定了12个基因,这些基因被组织成四个操纵子。预测有10个基因编码糖基转移酶、ATP结合盒多糖转运体或GDP-N-甲酰过氧胺生物合成所需的酶。OPS基因簇中的另外两个基因galF和galU在OPS生物合成中没有明确的功能;然而,后一个基因似乎对O:9至关重要。使用缺乏这些LPS部分之一或两者的同基因突变体研究了O:9 OPS和OC的生物学功能。我们发现OPS和OC赋予对人补体和多粘菌素B的抗性;仅在没有OC的情况下才能观察到OPS对多粘菌素B抗性的影响。

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