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首页> 外文期刊>Frontiers in Microbiology >Replicon-Based Typing of IncI-Complex Plasmids, and Comparative Genomics Analysis of IncIγ/K1 Plasmids
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Replicon-Based Typing of IncI-Complex Plasmids, and Comparative Genomics Analysis of IncIγ/K1 Plasmids

机译:IncI-Complex质粒基于复制子的分型和IncIγ/ K1质粒的比较基因组学分析

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IncI-complex plasmids can be divided into seven subgroups IncI1, IncI2, IncIγ, IncB/O, IncK1, IncK2, and IncZ. In this study, a replicon-based scheme was proposed for typing IncI-complex plasmids into four separately clustering subgroups IncI2, IncI1/B/O, IncIγ/K1 and IncK2/Z, the last three of which were combined from IncI1 and IncB/O, IncIγ and IncK1, and IncK2 and IncZ, respectively. Four IncIγ/K1 plasmids p205880-NR2, p14E509-CTXM, p11011-CTXM and p61806-CTXM were fully sequenced and compared with IncIγ/K1 reference pCT, IncI2 reference R721, IncI1/B/O reference R64 and IncK2/Z reference pO26-CRL-125. These plasmids shared conserved gene organization in the replication and conjugal transfer regions, but displaying considerable sequence diversity among different subgroups. Remarkable modular differences were observed in the maintenance and transfer leading regions. p205880-NR2 contained no resistance genes or accessory modules, while the other seven plasmids acquired one or more accessory modules, which harbored mobile elements [including unit transposons, insertion sequence (IS)-based transposition units and individual IS elements] and associated resistance markers (especially including those involved in resistance to β-lactams, aminoglycosides, tetracyclins, phenicols, streptomycins, trimethoprims, sulphonamides, tunicamycins and erythromycins). Data presented here provided a deeper insight into diversification and evolution of IncI-complex plasmids.
机译:IncI复合质粒可分为七个亚组IncI1,IncI2,IncIγ,IncB / O,IncK1,IncK2和IncZ。在这项研究中,提出了一种基于复制子的方案,用于将IncI-复杂质粒分为四个单独的聚类亚组IncI2,IncI1 / B / O,IncIγ/ K1和IncK2 / Z,其中最后三个是IncI1和IncB / O,IncIγ和IncK1,以及IncK2和IncZ。对四个IncIγ/ K1质粒p205880-NR2,p14E509-CTXM,p11011-CTXM和p61806-CTXM进行了完整测序,并与IncIγ/ K1参考pCT,IncI2参考R721,IncI1 / B / O参考R64和IncK2 / Z参考pO26-进行了比较。 CRL-125。这些质粒在复制和结合转移区域共享保守的基因组织,但是在不同亚组之间显示出相当大的序列多样性。在维护和转移领先地区观察到明显的模块差异。 p205880-NR2不包含抗性基因或辅助模块,而其他七个质粒获得一个或多个辅助模块,这些模块包含移动元件[包括单位转座子,基于插入序列(IS)的转座单位和单个IS元件]和相关的抗性标记(尤其包括那些对β-内酰胺类,氨基糖苷类,四环素,酚类,链霉素,甲氧苄啶,磺胺类,衣霉素和红霉素有抗性的药物)。此处提供的数据为IncI复杂质粒的多样化和进化提供了更深入的见解。

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