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首页> 外文期刊>Journal of Clinical Microbiology >Outbreak Investigation Using High-Throughput Genome Sequencing within a Diagnostic Microbiology Laboratory
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Outbreak Investigation Using High-Throughput Genome Sequencing within a Diagnostic Microbiology Laboratory

机译:在诊断微生物学实验室中使用高通量基因组测序进行暴发调查

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Next-generation sequencing (NGS) of bacterial genomes has recently become more accessible and is now available to the routine diagnostic microbiology laboratory. However, questions remain regarding its feasibility, particularly with respect to data analysis in nonspecialist centers. To test the applicability of NGS to outbreak investigations, Ion Torrent sequencing was used to investigate a putative multidrug-resistant Escherichia coli outbreak in the neonatal unit of the Mercy Hospital for Women, Melbourne, Australia. Four suspected outbreak strains and a comparator strain were sequenced. Genome-wide single nucleotide polymorphism (SNP) analysis demonstrated that the four neonatal intensive care unit (NICU) strains were identical and easily differentiated from the comparator strain. Genome sequence data also determined that the NICU strains belonged to multilocus sequence type 131 and carried the blaCTX-M-15 extended-spectrum beta-lactamase. Comparison of the outbreak strains to all publicly available complete E. coli genome sequences showed that they clustered with neonatal meningitis and uropathogenic isolates. The turnaround time from a positive culture to the completion of sequencing (prior to data analysis) was 5 days, and the cost was approximately $300 per strain (for the reagents only). The main obstacles to a mainstream adoption of NGS technologies in diagnostic microbiology laboratories are currently cost (although this is decreasing), a paucity of user-friendly and clinically focused bioinformatics platforms, and a lack of genomics expertise outside the research environment. Despite these hurdles, NGS technologies provide unparalleled high-resolution genotyping in a short time frame and are likely to be widely implemented in the field of diagnostic microbiology in the next few years, particularly for epidemiological investigations (replacing current typing methods) and the characterization of resistance determinants. Clinical microbiologists need to familiarize themselves with these technologies and their applications.
机译:细菌基因组的下一代测序(NGS)最近变得更加容易使用,现在可用于常规诊断微生物学实验室。但是,关于其可行性,尤其是在非专业中心的数据分析方面,仍然存在疑问。为了测试NGS在暴发调查中的适用性,使用离子洪流测序对澳大利亚墨尔本仁慈妇女医院的新生儿科中推定的耐多药大肠埃希菌进行了调查。对四个疑似暴发菌株和一个比较菌株进行了测序。全基因组单核苷酸多态性(SNP)分析表明,四个新生儿重症监护病房(NICU)菌株相同,很容易与对照菌株区分开。基因组序列数据还确定了NICU菌株属于多基因座序列类型131,并带有 bla CTX-M-15 超广谱β-内酰胺酶。暴发菌株与所有公开可获得的完整大肠杆菌基因组序列的比较表明,它们与新生儿脑膜炎和泌尿道致病菌分离株成簇。从阳性培养到测序完成(数据分析之前)的周转时间为5天,每个菌株的成本约为300美元(仅适用于试剂)。目前,诊断微生物学实验室采用NGS技术的主要障碍是成本(尽管正在降低),缺乏用户友好型和以临床为重点的生物信息学平台,以及研究环境之外缺乏基因组学专业知识。尽管有这些障碍,NGS技术仍可在短时间内提供无与伦比的高分辨率基因分型,并且可能在未来几年中广泛应用于诊断微生物学领域,尤其是用于流行病学研究(取代当前的分型方法)和抵抗因素。临床微生物学家需要熟悉这些技术及其应用。

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