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首页> 外文期刊>BMC Genomics >Pyrosequencing-based comparative genome analysis of the nosocomial pathogen Enterococcus faecium and identification of a large transferable pathogenicity island
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Pyrosequencing-based comparative genome analysis of the nosocomial pathogen Enterococcus faecium and identification of a large transferable pathogenicity island

机译:医院病原菌肠球菌基于焦磷酸测序的比较基因组分析和可转移的大致病岛的鉴定

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Background The Gram-positive bacterium Enterococcus faecium is an important cause of nosocomial infections in immunocompromized patients. Results We present a pyrosequencing-based comparative genome analysis of seven E. faecium strains that were isolated from various sources. In the genomes of clinical isolates several antibiotic resistance genes were identified, including the vanA transposon that confers resistance to vancomycin in two strains. A functional comparison between E. faecium and the related opportunistic pathogen E. faecalis based on differences in the presence of protein families, revealed divergence in plant carbohydrate metabolic pathways and oxidative stress defense mechanisms. The E. faecium pan-genome was estimated to be essentially unlimited in size, indicating that E. faecium can efficiently acquire and incorporate exogenous DNA in its gene pool. One of the most prominent sources of genomic diversity consists of bacteriophages that have integrated in the genome. The CRISPR-Cas system, which contributes to immunity against bacteriophage infection in prokaryotes, is not present in the sequenced strains. Three sequenced isolates carry the esp gene, which is involved in urinary tract infections and biofilm formation. The esp gene is located on a large pathogenicity island (PAI), which is between 64 and 104 kb in size. Conjugation experiments showed that the entire esp PAI can be transferred horizontally and inserts in a site-specific manner. Conclusions Genes involved in environmental persistence, colonization and virulence can easily be aquired by E. faecium. This will make the development of successful treatment strategies targeted against this organism a challenge for years to come.
机译:背景技术革兰氏阳性粪便肠球菌是免疫功能低下患者医院感染的重要原因。结果我们介绍了从多种来源分离的7种粪肠球菌菌株的基于焦磷酸测序的比较基因组分析。在临床分离株的基因组中,鉴定了几种抗生素抗性基因,包括在两个菌株中赋予对万古霉素抗性的vanA转座子。粪肠球菌和相关机会性病原体粪肠球菌之间的功能比较基于蛋白质家族存在的差异,揭示了植物碳水化合物代谢途径和氧化应激防御机制的差异。估计粪肠球菌的全基因组的大小基本上是无限的,这表明粪肠球菌可以有效地获取外源DNA并将其整合到其基因库中。基因组多样性的最主要来源之一是整合到基因组中的噬菌体。 CRISPR-Cas系统对原核生物中的噬菌体感染具有免疫力,但在测序菌株中却不存在。三个测序的分离物带有esp基因,该基因与尿路感染和生物膜形成有关。 esp基因位于一个大的致病岛(PAI)上,大小在64到104 kb之间。共轭实验表明,整个esp PAI可以水平转移,并以特定位点的方式插入。结论粪肠球菌很容易获得与环境持久性,定殖和毒力有关的基因。这将使针对该生物的成功治疗策略的发展成为未来几年的挑战。

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