Genetic characterisation of a large antibiotic resistant environmental ST131 E. coli plasmid using a long read hybrid assembly approach

Genetic characterisation of a large antibiotic resistant environmental ST131 E. coli plasmid using a long read hybrid assembly approach
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使用长读长混合组装方法对大型抗生素抗性环境 ST131 大肠杆菌质粒进行遗传表征

DOI:
10.1101/2020.06.16.155663
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发表时间:
2020
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影响因子:
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通讯作者:
James R
James R
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文献类型:
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作者:
James R

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大肠杆菌131型是一种全球传播的环境。大肠杆菌与质粒介导的blactx - m型扩展谱β -内酰胺酶(ESBLs)的捕获和传播有关。在更广泛的遗传背景下准确识别这些抗性基因,可以更好地理解环境中的选择和持久性机制。在这项研究中,我们使用一种新的DNA提取和富集方法,结合定制的长读支架混合组装和抛光管道,来鉴定先前在ST131环境中鉴定的质粒borneblaCTX-Mgene的遗传背景。coliisolate。这使我们能够识别出一个约100kb的环境质粒的完整结构,并进一步解析出blactx - mvariant到9blactx - m -27基因。与blactx - m -15的全局捕获和传播相关的上游IS26插入元件也在blaCTX-M-27附近被确定。此外,在该质粒上发现的共轭机制缺失,结合毒素-抗毒素和质粒分配系统,表明了一种垂直传播机制,以保持种群的持久性。
Escherichia coliStrain Type 131 are a globally disseminated environmentalE. colithat has been linked to the capture and spread of plasmid mediatedblaCTX-Mtype extended spectrum beta-lactamase (ESBLs). Accurately identifying such resistance genes in their wider genetic context provides a greater understanding of the mechanisms of selection and persistence in the environment. In this study we use a novel DNA extraction and enrichment method in combination with a custom long-read scaffold hybrid-assembly and polishing pipe line to identify the genetic context of the plasmid borneblaCTX-Mgene previously identified in an ST131 environmentalE. coliisolate. This has allowed us to discern the complete structure of a ~100kb environmental plasmid and further resolve theblaCTX-Mvariant to the group 9blaCTX-M-27gene. The upstream IS26 insertion element associated with the global capture and dissemination ofblaCTX-M-15was also identified in proximity to blaCTX-M-27. Furthermore, the lack of conjugative machinery identified on this plasmid, in combination with a toxin-antitoxin and plasmid partitioning system, indicates a mechanism of vertical transmission to maintain persistence in a population.
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