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O-antigen biosynthesis gene clusters of Escherichia albertii: their diversity and similarity to Escherichia coli gene clusters and the development of an O-genotyping method

机译:阿尔伯埃希氏菌的O抗原生物合成基因簇:其与大肠杆菌基因簇的多样性和相似性以及O基因分型方法的发展

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摘要

is a recently recognized human enteropathogen that is closely related to . In many Gram-negative bacteria, including , O-antigen variation has long been used for the serotyping of strains. In , while eight O-serotypes unique to this species have been identified, some strains have been shown to exhibit genetic or serological similarity to known / O-serotypes. However, the diversity of O-serotypes and O-antigen biosynthesis gene clusters (O-AGCs) of remains to be systematically investigated. Here, we analysed the O-AGCs of 65 strains and identified 40 O-genotypes (EAOgs) (named EAOg1–EAOg40). Analyses of the 40 EAOgs revealed that as many as 20 EAOgs exhibited significant genetic and serological similarity to the O-AGCs of known / O-serotypes, and provided evidence for the inter-species horizontal gene transfer of O-AGCs between and . Based on the sequence variation in the gene among the 40 EAOgs, we developed a multiplex PCR-based O-genotyping system for (EAO-genotyping PCR) and verified its usefulness by genotyping 278 strains from various sources. Although 225 (80.9 %) of the 278 strains could be genotyped, 51 were not assigned to any of the 40 EAOgs, indicating that further analyses are required to better understand the diversity of O-AGCs in and improve the EAO-genotyping PCR method. A phylogenetic view of strains sequenced so far is also presented with the distribution of the 40 EAOgs, which provided multiple examples for the intra-species horizontal transfer of O-AGCs in .
机译:乙型肝炎是最近被认可的与乙型肝炎有关的人类肠病原体。在许多革兰氏阴性细菌(包括)中,O抗原变异长期以来一直用于菌株的血清分型。在中,虽然已鉴定出该物种独特的八种O型血清型,但已显示某些菌株与已知的O型血清型具有遗传或血清学相似性。然而,O型血清型和O抗原生物合成基因簇(O-AGCs)的多样性仍有待系统研究。在这里,我们分析了65个菌株的O-AGC,并鉴定了40个O基因型(EAOgs)(命名为EAOg1-EAOg40)。对40种EAOgs的分析显示,多达20种EAOgs与已知/ O型血清型的O-AGCs表现出显着的遗传和血清学相似性,并为O-AGCs在和之间的种间水平基因转移提供了证据。基于40个EAOg中基因的序列变异,我们开发了基于多重PCR的O型分型系统(EAO型分型PCR),并通过对来自各种来源的278株进行基因分型验证了其有效性。尽管可以对278个菌株中的225个(占80.9%)进行基因分型,但40个EAOg中没有51个被分型,这表明需要进一步分析以更好地了解O-AGC的多样性并改善EAO基因分型PCR方法。通过40种EAOgs的分布,还显示了迄今为止已测序菌株的系统进化观点,为O-AGC在物种内水平转移提供了多个实例。

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