Chapman Paul, Forde Brian M, Roberts Leah W, Bergh Haakon, Vesey Debra, Jennison Amy V, Moss Susan, Paterson David L, Beatson Scott A, Harris Patrick N A
Infectious Diseases Unit, Royal Brisbane and Women's Hospital, Herston, QLD, Australia.
Infection Prevention and Control, Caboolture Hospital, Caboolture, QLD, Australia.
J Clin Microbiol. 2020 Apr 23;58(5). doi: 10.1128/JCM.01980-19.
species are problematic pathogens in neonatal units and may cause outbreaks, for which the sources of transmission may be challenging to elucidate. We describe the use of whole-genome sequencing (WGS) to investigate environmental sources of transmission during an outbreak of extended-spectrum-β-lactamase (ESBL)-producing colonizing neonates. Ceftriaxone-resistant spp. isolated from neonates (or their mothers) and the hospital environment were included. Short-read sequencing (Illumina) and long-read sequencing (MinION; Oxford Nanopore Technologies) were used to confirm species taxonomy, to identify antimicrobial resistance genes, and to determine phylogenetic relationships using single-nucleotide polymorphism profiling. A total of 21 organisms (10 patient-derived isolates and 11 environmental isolates) were sequenced. Standard laboratory methods identified the outbreak strain as an ESBL-producing , but taxonomic assignment from WGS data suggested closer identity to Strains isolated from multiple detergent-dispensing bottles were either identical or closely related by single-nucleotide polymorphism comparison. Detergent bottles contaminated by had been used for washing milk expression equipment. No new cases were identified once the detergent bottles were removed. Environmental reservoirs may be an important source in outbreaks of multidrug-resistant organisms. WGS, in conjunction with traditional epidemiological investigation, can be instrumental in revealing routes of transmission and guiding infection control responses.
某些菌种是新生儿病房中的问题病原体,可能引发疫情,其传播源可能难以查明。我们描述了如何使用全基因组测序(WGS)来调查产超广谱β-内酰胺酶(ESBL)的定植新生儿疫情期间的环境传播源。纳入了从新生儿(或其母亲)及医院环境中分离出的耐头孢曲松的特定菌种。使用短读长测序(Illumina)和长读长测序(MinION;牛津纳米孔技术公司)来确认菌种分类,鉴定抗菌药物耐药基因,并通过单核苷酸多态性分析确定系统发育关系。共对21个菌株(10个来自患者的分离株和11个环境分离株)进行了测序。标准实验室方法将疫情菌株鉴定为产ESBL的特定菌种,但WGS数据的分类归属表明其与另一菌种的亲缘关系更近。通过单核苷酸多态性比较,从多个洗涤剂分配瓶中分离出的菌株要么完全相同,要么密切相关。被特定菌种污染的洗涤剂瓶曾用于清洗吸奶器设备。一旦移除洗涤剂瓶,就未发现新病例。环境储源可能是多重耐药菌疫情的重要源头。WGS与传统流行病学调查相结合,有助于揭示传播途径并指导感染控制应对措施。