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Translatability of WGS typing results can simplify data exchange for surveillance and control of Listeria monocytogenes

机译:WGS键入结果的可通用性可以简化李斯特菌单核细胞增生的监测和控制的数据交换

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Where classical epidemiology has proven to be inadequate for surveillance and control of foodborne pathogens, molecular epidemiology, using genomic typing methods, can add value. However, the analysis of whole genome sequencing (WGS) data varies widely and is not yet fully harmonised. We used genomic data on 494 Listeria monocytogenes isolates from ready-to-eat food products and food processing environments deposited in the strain collection of the German National Reference Laboratory to compare various procedures for WGS data analysis and to evaluate compatibility of results. Two different core genome multilocus sequence typing (cgMLST) schemes, different reference genomes in single nucleotide polymorphism (SNP) analysis and commercial as well as open-source software were compared. Correlation of allele distances from the different cgMLST approaches was high, ranging from 0.97 to 1, and unified thresholds yielded higher clustering concordance than scheme-specific thresholds. The number of detected SNP differences could be increased up to a factor of 3.9 using a specific reference genome compared with a general one. Additionally, specific reference genomes improved comparability of SNP analysis results obtained using different software tools. The use of a closed or a draft specific reference genome did not make a difference. The harmonisation of WGS data analysis will finally guarantee seamless data exchange, but, in the meantime, knowledge on threshold values that lead to comparable clustering of isolates by different methods may improve communication between laboratories. We therefore established a translation code between commonly applied cgMLST and SNP methods based on optimised clustering concordances. This code can work as a first filter to identify WGS-based typing matches resulting from different methods, which opens up a new perspective for data exchange and thereby accelerates time-critical analyses, such as in outbreak investigations.
机译:古典流行病学已被证明是对食源性病原体的监测和控制不足,使用基因组类型方法的分子流行病学可以增加价值。然而,全基因组测序(WGS)数据的分析广泛变化,并且尚未完全协调。我们在494次Histeria单核细胞增生中使用基因组数据,从即食食品和食品加工环境中沉积在德国国家参考实验室的应变收集中,比较WGS数据分析的各种程序,并评估结果的兼容性。比较了两种不同的核心基因组多层序列键入(CGMLST)方案,单一核苷酸多态性(SNP)分析和商业以及开源软件中的不同参考基因组。来自不同CGMLST方法的等位基因距离的相关性高,范围为0.97至1,并且统一的阈值产生比方案特定阈值更高的聚类一致性。与一般的基因组相比,检测到的SNP差异的数量可以增加至3.9系数。另外,特定参考基因组改善了使用不同软件工具获得的SNP分析结果的可比性。使用关闭或特定参考基因组没有产生差异。 WGS数据分析的协调将最终保证无缝数据交换,但是,在此期间,有关通过不同方法的与分离液相当聚类的阈值的知识可以改善实验室之间的沟通。因此,我们在常用的CGMLST和SNP方法之间建立了转换代码,基于优化的聚类齐全。此代码可以作为第一个过滤器,以识别由不同方法产生的基于WG的键入匹配,这为数据交换开辟了新的透视,从而加速了爆发调查的时间关键分析。

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