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A Validation Approach of an End-to-End Whole Genome Sequencing Workflow for Source Tracking of Listeria monocytogenes and Salmonella enterica

机译:端到端全基因组测序工作流程用于单核细胞增生李斯特菌和肠炎沙门氏菌来源追踪的验证方法

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摘要

Whole genome sequencing (WGS), using high throughput sequencing technology, reveals the complete sequence of the bacterial genome in a few days. WGS is increasingly being used for source tracking, pathogen surveillance and outbreak investigation due to its high discriminatory power. In the food industry, WGS used for source tracking is beneficial to support contamination investigations. Despite its increased use, no standards or guidelines are available today for the use of WGS in outbreak and/or trace-back investigations. Here we present a validation of our complete (end-to-end) WGS workflow for Listeria monocytogenes and Salmonella enterica including: subculture of isolates, DNA extraction, sequencing and bioinformatics analysis. This end-to-end WGS workflow was evaluated according to the following performance criteria: stability, repeatability, reproducibility, discriminatory power, and epidemiological concordance. The current study showed that few single nucleotide polymorphism (SNPs) were observed for L. monocytogenes and S. enterica when comparing genome sequences from five independent colonies from the first subculture and five independent colonies after the tenth subculture. Consequently, the stability of the WGS workflow for L. monocytogenes and S. enterica was demonstrated despite the few genomic variations that can occur during subculturing steps. Repeatability and reproducibility were also demonstrated. The WGS workflow was shown to have a high discriminatory power and has the ability to show genetic relatedness. Additionally, the WGS workflow was able to reproduce published outbreak investigation results, illustrating its capability of showing epidemiological concordance. The current study proposes a validation approach comprising all steps of a WGS workflow and demonstrates that the workflow can be applied to L. monocytogenes or S. enterica.
机译:使用高通量测序技术的全基因组测序(WGS)可在几天内揭示细菌基因组的完整序列。 WGS具有很高的区分能力,因此越来越多地用于源跟踪,病原体监视和疾病爆发调查。在食品工业中,用于源跟踪的WGS有助于支持污染调查。尽管增加了使用量,但当今尚无关于在爆发和/或追溯调查中使用WGS的标准或指南。在这里,我们对单核细胞增生李斯特菌和肠炎沙门氏菌的完整(端对端)WGS工作流程进行了验证,包括:分离株的继代培养,DNA提取,测序和生物信息学分析。根据以下性能标准评估了这种端到端WGS工作流程:稳定性,可重复性,可再现性,歧视能力和流行病学一致性。当前的研究表明,当比较来自第一次传代培养的五个独立菌落和第十次传代培养后的五个独立菌落的基因组序列时,单核细胞增生李斯特菌和小肠链球菌的单核苷酸多态性(SNPs)很少。因此,尽管在亚培养步骤中可能发生一些基因组变异,但仍证明了单核细胞增生李斯特氏菌和小肠链球菌的WGS工作流程的稳定性。还证明了可重复性和可重复性。事实证明,WGS工作流程具有很高的辨别力,并具有显示遗传相关性的能力。此外,WGS工作流能够复制已发布的暴发调查结果,从而说明了其显示流行病学一致性的能力。当前的研究提出了一种验证方法,该方法包括WGS工作流程的所有步骤,并证明该工作流程可以应用于单核细胞增生李斯特菌或小肠链球菌。

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