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Analysis of a Clostridium difficile PCR ribotype 078 100 kilobase island reveals the presence of a novel transposon, Tn6164

机译:艰难梭菌pCR核糖体078 100千碱基岛的分析显示存在新的转座子,Tn6164

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摘要

BACKGROUND: Clostridium difficile is the main cause of antibiotic associated diarrhea. In the past decade, the number of C. difficile patients has increased dramatically, coinciding with the emergence of two PCR ribotypes 027 and 078. PCR ribotype 078 is also frequently found during C. difficile outbreaks in pigfarms. Previously, the genome of the PCR ribotype 078 strain M120, a human isolate, was described to contain a unique insert of 100 kilobases. RESULTS: Analysis of this insert revealed over 90 open reading frames, encoding proteins originating from transposons, phages and plasmids. The insert was shown to be a transposon (Tn6164), as evidenced by the presence of an excised and circularised molecule, containing the ligated 5'and 3'ends of the insert. Transfer of the element could not be shown through filter-mating experiments. Whole genome sequencing of PCR ribotype 078 strain 31618, isolated from a diarrheic piglet, showed that Tn6164 was not present in this strain. To test the prevalence of Tn6164, a collection of 231 Clostridium difficile PCR ribotype 078 isolates from human (n = 173) and porcine (n = 58) origin was tested for the presence of this element by PCR. The transposon was present in 9 human, tetracycline resistant isolates, originating from various countries in Europe, and none of the pig strains. Nine other strains, also tetracycline resistant human isolates, contained half of the transposon, suggesting multiple insertion steps yielding the full Tn6164. Other PCR ribotypes (n = 66) were all negative for the presence of the transposon. Multi locus variable tandem repeat analysis revealed genetic relatedness among transposon containing isolates. Although the element contained several potential antibiotic resistance genes, it did not yield a readily distinguishable phenotype. CONCLUSIONS: Tn6164 is a newly described transposon, occurring sporadically in C. difficile PCR ribotype 078 strains. Although no transfer of the element could be shown, we hypothesize that the element could serve as a reservoir of antibiotic resistance genes for other bacteria. Further research is needed to investigate the transfer capabilities of the element and to substantiate the possible role of Tn6164 as a source of antibiotic resistance genes for other gut pathogens.
机译:背景:艰难梭菌是引起抗生素相关性腹泻的主要原因。在过去的十年中,艰难梭菌患者的数量急剧增加,这与两个PCR核型027和078的出现相吻合。PCR核型078在猪场的艰难梭菌暴发期间也很常见。以前,PCR核型078菌株M120(人类分离株)的基因组被描述为包含100千个碱基的独特插入片段。结果:对该插入片段的分析揭示了90多个开放阅读框,它们编码源自转座子,噬菌体和质粒的蛋白质。插入物被证明是转座子(Tn6164),这是通过存在包含插入物的5'和3'末端连接的切离和环化的分子来证明的。元素的转移无法通过过滤器配合实验显示出来。从腹泻仔猪中分离得到的PCR核型078菌株31618的全基因组测序表明,该菌株中不存在Tn6164。为了测试Tn6164的流行程度,通过PCR检测了来自人类(n = 173)和猪(n = 58)来源的231株艰难梭菌PCR核型078分离株的集合。转座子存在于9种抗四环素的人类分离株中,这些分离株来自欧洲各个国家,但没有一种猪株。其他九个菌株,也具有四环素抗性的人类分离株,含有一半的转座子,表明多个插入步骤可产生完整的Tn6164。其他PCR核型(n = 66)对转座子的存在均为阴性。多基因座串联串联重复分析揭示了转座子分离株之间的遗传相关性。尽管该元素包含几个潜在的抗生素抗性基因,但它没有产生易于区分的表型。结论:Tn6164是一个新描述的转座子,偶尔出现在艰难梭菌PCR核型078菌株中。尽管没有显示出该元素的转移,但我们推测该元素可以作为其他细菌的抗生素抗性基因的贮藏库。需要进一步的研究以调查该元素的转移能力,并证实Tn6164作为其他肠道病原体抗生素抗性基因来源的可能作用。

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