Shenzhen Key Laboratory for Food Biological Safety Control, Food Safety and Technology Research Centre, The Hong Kong PolyU Shenzhen Research Institute, Shenzhen, P. R. China.
State Key Laboratory of Chirosciences, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong.
J Antimicrob Chemother. 2017 Oct 1;72(10):2750-2754. doi: 10.1093/jac/dkx238.
To characterize a novel virulence-resistance plasmid pSE380T carried by a Salmonella enterica serotype Enteritidis clinical strain SE380.
The plasmid pSE380T was conjugated to Escherichia coli strain J53 and sequenced by PacBio RSII, followed by subsequent annotation and genetic analysis.
Sequence analysis of this plasmid revealed that the entire Salmonella Enteritidis-specific virulence plasmid, pSEN, had been incorporated into an IncHI2 MDR plasmid, which comprises the cephalosporin and fosfomycin resistance determinants blaCTX-M-14 and fosA3. Based on BLAST analysis and scrutiny of insertion footprints, the insertion event was found to involve a replicative transposition process mediated by IS26, an IS element frequently detected in various resistance plasmids. The resulting pSE380T plasmid also comprises backbone elements of IncHI2 and IncFIA plasmids, producing a rare fusion product that simultaneously encodes functional features of both, i.e. virulence, resistance and high transmissibility.
This is a novel hybrid plasmid mediating MDR and virulence from a clinical Salmonella Enteritidis strain. This plasmid is likely to be transmissible amongst various serotypes of Salmonella and other Enterobacteriaceae species, rendering a wide range of bacterial pathogens resistant to cephalosporins and fosfomycin, and further enhancing their virulence potential. It will be important to monitor the spread and further evolution of this plasmid among the Enterobacteriaceae strains.
分析一株肠炎沙门氏菌临床分离株 SE380 携带的新型毒力-耐药性质粒 pSE380T。
将质粒 pSE380T 经接合转移至大肠杆菌 J53 中,并使用 PacBio RSII 进行测序,随后进行注释和遗传分析。
该质粒的序列分析表明,整个肠炎沙门氏菌特异性毒力质粒 pSEN 已整合到一个 IncHI2 MDR 质粒中,该质粒包含头孢菌素和磷霉素耐药决定簇 blaCTX-M-14 和 fosA3。基于 BLAST 分析和插入足迹的检查,发现插入事件涉及由 IS26 介导的复制转位过程,IS26 是一种在各种耐药质粒中经常检测到的 IS 元件。由此产生的 pSE380T 质粒还包含 IncHI2 和 IncFIA 质粒的骨架元件,产生一种罕见的融合产物,同时编码两者的功能特征,即毒力、耐药性和高传播性。
这是一种介导临床肠炎沙门氏菌 MDR 和毒力的新型杂合质粒。该质粒可能在各种沙门氏菌血清型和其他肠杆菌科物种之间传播,使多种细菌病原体对头孢菌素和磷霉素产生耐药性,并进一步增强其毒力潜力。监测这种质粒在肠杆菌科菌株中的传播和进一步进化将非常重要。