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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Characterization of Enterobacteriaceae producing OXA-48-like carbapenemases in the UK
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Characterization of Enterobacteriaceae producing OXA-48-like carbapenemases in the UK

机译:英国产肠杆菌科细菌产生OXA-48样碳青霉烯酶的表征

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摘要

Objectives: To characterize UK clinical isolates of Enterobacteriaceae producing OXA-48-like carbapenemases and to compare their resistance plasmids. Methods: Twenty-six enterobacteria producing OXA-48-like enzymes were studied. These were from 22 diverse hospitals in the UK. Isolates of Escherichia coli and Klebsiella pneumoniae were assigned to clonal lineages by multilocus sequence typing. Carbapenemase genes and their genetic environments were characterized by PCR and sequencing. Resistance plasmids were transferred by transformation or conjugation and compared by restriction analysis and PCR for genes encoding critical plasmid functions. Results: Thirteen isolates of K. pneumoniae, 10 E. coli and 2 Enterobacter cloacae harboured a classical bla OXA-48 gene; the K. pneumoniae isolates belonged to 11 sequence types (STs) and the E. coli to 7 STs, including ST131 and ST38. The bla OXA-48 genes were located within either Tn1999 or Tn1999.2 transposons on related ~50 kb or ~62 kb plasmids, which lacked other resistance genes or, in one isolate, on an ~140 kb plasmid that also encoded OXA-9 and CTX-M group-9 β-lactamases. One India-linked K. pneumoniae isolate had a blaOXA-181 gene in association with an ISEcp1 insertion sequence on a 7 kb plasmid. Conclusions: Horizontal transfer of related plasmids has facilitated the spread of OXA-48 carbapenemase into multiple strains of several Enterobacteriaceae species. The clonal diversity of the producers suggests repeated introduction into the UK. Low carbapenem MICs for some producers complicates detection and creates a risk for unrecognized spread.
机译:目的:鉴定英国产肠杆菌的产OXA-48样碳青霉烯酶的菌株,并比较其耐药质粒。方法:研究了26种肠杆菌产生OXA-48样酶。这些来自英国的22家不同的医院。通过多基因座序列分型将大肠杆菌和肺炎克雷伯菌的分离株分配给克隆谱系。通过PCR和测序对碳青霉烯酶基因及其遗传环境进行了表征。通过转化或结合转移抗性质粒,并通过限制性分析和PCR比较编码关键质粒功能的基因。结果:13株肺炎克雷伯菌,10株大肠杆菌和2株阴沟肠杆菌带有经典的bla OXA-48基因。肺炎克雷伯菌分离物属于11个序列类型(STs),而大肠杆菌属于7个STs,包括ST131和ST38。 bla OXA-48基因位于相关的〜50 kb或〜62 kb质粒上的Tn1999或Tn1999.2转座子中,这些质粒缺乏其他抗性基因,或者在一个分离株中,也编码〜140 kb质粒中也编码OXA-9和CTX-M第9组β-内酰胺酶。一种印度连锁的肺炎克雷伯菌分离株具有blaOXA-181基因,该基因与7 kb质粒上的ISEcp1插入序列相关。结论:相关质粒的水平转移促进了OXA-48碳青霉烯酶向几种肠杆菌科细菌的多种菌株中的传播。生产者的克隆多样性表明,他们反复被引入英国。对于一些生产者而言,低碳青霉烯类MICs使检测复杂化,并存在无法识别的传播风险。

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