Compatibility of whole-genome sequencing data from Illumina and Ion Torrent technologies in genome comparison analysis of Listeria monocytogenes.

IF 4 2区 生物学 Q1 GENETICS & HEREDITY
Stefanie Lüth, Jannika Fuchs, Carlus Deneke
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引用次数: 0

Abstract

Whole-genome sequencing (WGS) has become the key approach for molecular surveillance of Listeria monocytogenes. Genome comparison analysis can reveal transmission routes that cannot be found with classic epidemiology. A widespread standard for use in genome comparison analysis involves data from short-read sequencing, generated on Illumina or Ion Torrent devices. To date, little is known about the compatibility of data from both platforms. This knowledge is essential when it comes to the central analysis of data, for example, in the case of outbreaks. We used WGS data from 47 L. monocytogenes isolates of the strain collection of the German National Reference Laboratory for L. monocytogenes, generated on either Illumina or Ion Torrent devices, to analyse the impact of the sequencing technology on downstream analyses. In our study, only the assembler SPAdes delivered qualitatively comparable results. In the gene-based core genome multilocus sequence typing (cgMLST), the same-strain allele discrepancy between the platforms was 14.5 alleles on average, which is well above the threshold of 7 alleles routinely used for cluster detection in L. monocytogenes. An application of a strict frameshift filter in cgMLST analysis could push the mean discrepancy below this threshold but reduced discriminatory power. The impact of the platform on the read-based single nucleotide polymorphism analysis was lower than that on the cgMLST. Overall, it was possible to improve compatibility in various ways, but perfect compatibility could not be achieved.

单增李斯特菌基因组比较分析中Illumina全基因组测序数据与Ion Torrent技术的兼容性。
全基因组测序(WGS)已成为单核增生李斯特菌分子监测的重要手段。基因组比较分析可以揭示经典流行病学无法发现的传播途径。在基因组比较分析中广泛使用的标准包括短读测序数据,这些数据是在Illumina或Ion Torrent设备上生成的。迄今为止,人们对这两个平台的数据兼容性知之甚少。这方面的知识对于数据的中心分析至关重要,例如,在疫情的情况下。我们使用来自德国国家单核增生乳杆菌参考实验室菌株收集的47株单胞增生乳杆菌的WGS数据,在Illumina或Ion Torrent设备上生成,分析测序技术对下游分析的影响。在我们的研究中,只有汇编SPAdes提供了定性可比的结果。在基于基因的核心基因组多位点序列分型(cgMLST)中,平台间的同株等位基因差异平均为14.5个,远高于单核增生乳杆菌常规聚类检测的7个等位基因的阈值。在cgMLST分析中应用严格移码滤波器可以使平均差值低于该阈值,但可以降低区分能力。该平台对基于reads的单核苷酸多态性分析的影响低于cgMLST。总的来说,可以通过各种方式提高兼容性,但无法实现完美的兼容性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial Genomics
Microbial Genomics Medicine-Epidemiology
CiteScore
6.60
自引率
2.60%
发文量
153
审稿时长
12 weeks
期刊介绍: Microbial Genomics (MGen) is a fully open access, mandatory open data and peer-reviewed journal publishing high-profile original research on archaea, bacteria, microbial eukaryotes and viruses.
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