Division of Microbiology, Osaka Institute of Public Health, 8-34 Tojo-cho, Tennoji-ku, Osaka, Japan.
Division of Microbiology, Osaka Institute of Public Health, 8-34 Tojo-cho, Tennoji-ku, Osaka, Japan.
J Glob Antimicrob Resist. 2021 Mar;24:220-227. doi: 10.1016/j.jgar.2020.11.028. Epub 2020 Dec 29.
The spread of carbapenemase-producing Enterobacterales (CPE) with colistin resistance is a critical public health issue. We genetically characterized the clinical isolate Enterobacter roggenkampii OIPH-N260, which harboured carbapenemase genes bla and bla with multiple resistance genes, including mcr-9 and bla.
This isolate was characterized by whole-genome sequencing, comparative analysis of resistance plasmids, susceptibility tests, bacterial conjugation, S1-nuclease digested pulsed-field-gel electrophoresis, and Southern blot hybridization.
The OIPH-N260 isolate exhibited resistance to most β-lactams and colistin. It co-harboured two resistance plasmids, the bla- and bla-encoding IncP6 plasmid pN260-3 and mcr-9- and bla-encoding IncHI2 plasmid pN260-1. The comparative analysis of pN260-3 indicated that a unique bla-surrounding region was inserted into the bla-encoding plasmid with the mobile element IS26, which plays an important role in the spread of resistance genes. pN260-1 did not possess the mcr-9 expression regulative gene qseBC. Both plasmids were transferable into other bacterial species via conjugation.
This is the first study to report not only a bla and bla co-encoding plasmid, but also the co-harbouring of another plasmid carrying mcr-9 and bla in Enterobacter cloacae complex. The development of advanced resistance via IS26-mediated insertion and the co-harbouring of resistance plasmids highlights the need to monitor for resistance genes in CPE.
产碳青霉烯酶肠杆菌科(CPE)与多粘菌素耐药的传播是一个关键的公共卫生问题。我们对携带碳青霉烯酶基因 bla 和 bla 以及包括 mcr-9 和 bla 在内的多种耐药基因的临床分离株 Enterobacter roggenkampii OIPH-N260 进行了基因特征分析。
通过全基因组测序、耐药质粒的比较分析、药敏试验、细菌接合、S1 核酸酶消化脉冲场凝胶电泳和 Southern 印迹杂交对该分离株进行了特征分析。
OIPH-N260 分离株对大多数β-内酰胺类药物和多粘菌素表现出耐药性。它同时携带两个耐药质粒,bla 和 bla 编码的 IncP6 质粒 pN260-3 和 mcr-9 和 bla 编码的 IncHI2 质粒 pN260-1。pN260-3 的比较分析表明,一个独特的 bla 周围区域插入了 bla 编码质粒,其中移动元件 IS26 发挥了重要作用,推动了耐药基因的传播。pN260-1 不具有 mcr-9 表达调控基因 qseBC。这两个质粒都可以通过接合转移到其他细菌种属中。
这是首次报道bla 和 bla 同时编码质粒的研究,也是首次在阴沟肠杆菌复合体中同时发现携带 mcr-9 和 bla 的另一个质粒。IS26 介导的插入和耐药质粒的共携带导致了耐药性的发展,这凸显了需要监测 CPE 中的耐药基因。