Centre for Infectious Disease Control (CIb), National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Centre for Infectious Disease Control (CIb), National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Clin Microbiol Infect. 2020 Oct;26(10):1412.e7-1412.e12. doi: 10.1016/j.cmi.2020.01.027. Epub 2020 Feb 5.
Carbapenem resistance mediated by mobile genetic elements has emerged worldwide and has become a major public health threat. To gain insight into the molecular epidemiology of carbapenem resistance in The Netherlands, Dutch medical microbiology laboratories are requested to submit suspected carbapenemase-producing Enterobacterales (CPE) to the National Institute for Public Health and the Environment as part of a national surveillance system.
Meropenem MICs and species identification were confirmed by E-test and MALDI-TOF and carbapenemase production was assessed by the Carbapenem Inactivation Method. Of all submitted CPE, one species/carbapenemase gene combination per person per year was subjected to next-generation sequencing (NGS).
In total, 1838 unique isolates were received between 2014 and 2018, of which 892 were unique CPE isolates with NGS data available. The predominant CPE species were Klebsiella pneumoniae (n = 388, 43%), Escherichia coli (n = 264, 30%) and Enterobacter cloacae complex (n = 116, 13%). Various carbapenemase alleles of the same carbapenemase gene resulted in different susceptibilities to meropenem and this effect varied between species. Analyses of NGS data showed variation of prevalence of carbapenemase alleles over time with bla being predominant (38%, 336/892), followed by bla (16%, 145/892). For the first time in the Netherlands, bla, bla and bla were detected. The genetic background of K. pneumoniae and E. coli isolates was highly diverse.
The CPE population in the Netherlands is diverse, suggesting multiple introductions. The predominant carbapenemase alleles are bla and bla. There was a clear association between species, carbapenemase allele and susceptibility to meropenem.
由移动遗传元件介导的碳青霉烯耐药性已在全球范围内出现,并已成为主要的公共卫生威胁。为了深入了解荷兰碳青霉烯耐药性的分子流行病学,荷兰医学微生物学实验室被要求作为国家监测系统的一部分,将疑似产碳青霉烯酶肠杆菌科(CPE)送交国家公共卫生和环境研究所。
采用 E 试验和 MALDI-TOF 确认美罗培南 MIC 和种属鉴定,采用碳青霉烯失活法评估碳青霉烯酶的产生。在所有提交的 CPE 中,每年每人每种/碳青霉烯酶基因组合进行下一代测序(NGS)。
在 2014 年至 2018 年间共收到 1838 个独特的分离株,其中 892 个是具有 NGS 数据的独特 CPE 分离株。主要的 CPE 种类是肺炎克雷伯菌(n=388,43%)、大肠杆菌(n=264,30%)和阴沟肠杆菌复合群(n=116,13%)。同一碳青霉烯酶基因的不同碳青霉烯酶等位基因导致对美罗培南的不同敏感性,这种影响在不同的物种之间有所不同。对 NGS 数据的分析表明,随着时间的推移,碳青霉烯酶等位基因的流行率存在差异,其中 bla 占主导地位(38%,336/892),其次是 bla (16%,145/892)。在荷兰,首次检测到 bla 、 bla 和 bla 。肺炎克雷伯菌和大肠杆菌分离株的遗传背景高度多样化。
荷兰的 CPE 人群多样化,提示存在多次传入。主要的碳青霉烯酶等位基因是 bla 和 bla 。种属、碳青霉烯酶等位基因与对美罗培南的敏感性之间存在明显的关联。