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首页> 外文期刊>Eurosurveillance >Genetic diversity and delineation of Salmonella Agona outbreak strains by next generation sequencing, Bavaria, Germany, 1993 to 2018
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Genetic diversity and delineation of Salmonella Agona outbreak strains by next generation sequencing, Bavaria, Germany, 1993 to 2018

机译:沙门氏菌Agona暴发菌株的遗传多样性和下一代测序方法的鉴定,德国巴伐利亚,1993年至2018年

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BackgroundIn 2017, a food-borne Salmonella Agona outbreak caused by infant milk products from a French supplier occurred in Europe. Simultaneously, S. Agona was detected in animal feed samples in Bavaria.AimUsing next generation sequencing (NGS) and three data analysis methods, this study’s objectives were to verify clonality of the Bavarian feed strains, rule out their connection to the outbreak, explore the genetic diversity of Bavarian S. Agona isolates from 1993 to 2018 and compare the analysis approaches employed, for practicality and ability to delineate outbreaks caused by the genetically monomorphic Agona serovar.MethodsIn this observational retrospective study, three 2017 Bavarian feed isolates were compared to a French outbreak isolate and 48 S. Agona isolates from our strain collections. The later included human, food, feed, veterinary and environmental isolates, of which 28 were epidemiologically outbreak related. All isolates were subjected to NGS and analysed by: (i) a publicly available species-specific core genome multilocus sequence typing (cgMLST) scheme, (ii) single nucleotide polymorphism phylogeny and (iii) an in-house serovar-specific cgMLST scheme. Using additional international S. Agona outbreak NGS data, the cluster resolution capacity of the two cgMLST schemes was assessed.ResultsWe could prove clonality of the feed isolates and exclude their relation to the French outbreak. All approaches confirmed former Bavarian epidemiological clusters.ConclusionEven for S. Agona, species-level cgMLST can produce reasonable resolution, being standardisable by public health laboratories. For single samples or homogeneous sample sets, higher resolution by serovar-specific cgMLST or SNP genotyping can facilitate outbreak investigations.
机译:背景2017年,欧洲发生了由法国供应商的婴儿奶制品引起的食源性沙门氏菌Agona爆发。同时,在巴伐利亚州的动物饲料样本中检测到了Agona S.Agona,旨在通过下一代测序(NGS)和三种数据分析方法来验证巴伐利亚饲料株的克隆性,排除它们与疫情的联系,探索从1993年到2018年对巴伐利亚S.Agona分离株的遗传多样性进行了比较,并比较了分析方法的适用性和能力,以描述由基因单态Agona血清型引起的暴发。方法在这项观察性回顾性研究中,将3株2017年巴伐利亚饲料分离株与法国从我们的毒株中分离出暴发分离株和48个S. Agona分离株。后者包括人类,食品,饲料,兽医和环境分离株,其中28种与流行病爆发有关。所有分离物均经过NGS鉴定,并通过以下方法进行分析:(i)可公开获得的物种特异性核心基因组多基因座序列分型(cgMLST)方案,(ii)单核苷酸多态性系统发育和(iii)内部血清素特异性cgMLST方案。使用其他国际性的S. Agona爆发NGS数据,评估了这两种cgMLST方案的集群分辨能力。结果我们可以证明饲料分离株的克隆性,并排除它们与法国爆发的关系。所有方法都证实了前巴伐利亚的流行病学集群。结论即使对于S. Agona,物种水平的cgMLST也可以产生合理的分辨率,并且可以通过公共卫生实验室进行标准化。对于单个样本或同质样本集,通过血清特异性cgMLST或SNP基因分型获得更高的分辨率可以促进暴发调查。

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