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首页> 外文期刊>Mobile DNA >Characterisation of mobile genetic elements in Mycoplasma hominis with the description of ICEHo-II, a variant mycoplasma integrative and conjugative element
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Characterisation of mobile genetic elements in Mycoplasma hominis with the description of ICEHo-II, a variant mycoplasma integrative and conjugative element

机译:用冰波-II的描述,一种变体支原体整合和共轭元素

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Mobile genetic elements are found in genomes throughout the microbial world, mediating genome plasticity and important prokaryotic phenotypes. Even the cell wall-less mycoplasmas, which are known to harbour a minimal set of genes, seem to accumulate mobile genetic elements. In Mycoplasma hominis, a facultative pathogen of the human urogenital tract and an inherently very heterogeneous species, four different MGE-classes had been detected until now: insertion sequence ISMhom-1, prophage MHoV-1, a tetracycline resistance mediating transposon, and ICEHo, a species-specific variant of a mycoplasma integrative and conjugative element encoding a T4SS secretion system (termed MICE). To characterize the prevalence of these MGEs, genomes of 23?M. hominis isolates were assembled using whole genome sequencing and bioinformatically analysed for the presence of mobile genetic elements. In addition to the previously described MGEs, a new ICEHo variant was found, which we designate ICEHo-II. Of 15 ICEHo-II genes, five are common MICE genes; eight are unique to ICEHo-II; and two represent a duplication of a gene also present in ICEHo-I. In 150?M. hominis isolates and based on a screening PCR, prevalence of ICEHo-I was 40.7%; of ICEHo-II, 28.7%; and of both elements, 15.3%. Activity of ICEHo-I and -II was demonstrated by detection of circularized extrachromosomal forms of the elements through PCR and subsequent Sanger sequencing. Nanopore sequencing enabled the identification of mobile genetic elements and of ICEHo-II, a novel MICE element of M. hominis, whose phenotypic impact and potential impact on pathogenicity can now be elucidated.
机译:在整个微生物世界中的基因组中发现流动遗传元件,介导基因组可塑性和重要原核表型。即使是较少含有最小基因集的细胞壁的支原体,似乎也积累了移动遗传元素。在支原体中,迄今为止检测到人泌尿道和固有的异质物种,四种不同的MGE课程,直到现在:插入序列ISMHOM-1,前环素抵抗力介导转座子,冰川,一种特异性的经过型转基因聚合性和编码T4S分泌系统(称为小鼠)的聚合元素的特异性变体。表征这些升军的患病率,23米的基因组。使用全基因组测序组装Hominis分离株,并对移动遗传元件的存在进行生物信息分析。除了先前描述的升军之外,发现了一种新的冰波变体,我们指定了ICEHO-II。 15个冰波-II基因,五是常见的小鼠基因;八是冰波-II独有的;并且两个代表了Iceho-i中也存在的基因的重复。在150?m。 Hominis分离物并基于筛选PCR,Iceho-I的患病率为40.7%; Iceho-II,28.7%;并且两个元素,15.3%。通过通过PCR检测元素的圆形化的圆锥体形式形式和随后的Sanger测序来证明Iceho-I和-II的活性。纳米孔测序使得移动遗传元素和Iceho-II的鉴定,Mominis的新小鼠元素,现在可以阐明其表型抗冲击性和对致病性的潜在影响。

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