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利用下一代测序和数字 PCR 分析一起诺如病毒胃肠炎暴发涉及的冷冻草莓。

Analysis of frozen strawberries involved in a large norovirus gastroenteritis outbreak using next generation sequencing and digital PCR.

机构信息

German Federal Institute for Risk Assessment, Max-Dohrn-Str. 8-10, 10589, Berlin, Germany.

Friedrich Loeffler Institute, Südufer 10, 17493, Greifswald (Insel Riems), Germany.

出版信息

Food Microbiol. 2018 Dec;76:390-395. doi: 10.1016/j.fm.2018.06.019. Epub 2018 Jul 2.

DOI:10.1016/j.fm.2018.06.019
PMID:30166165
Abstract

Virus-contaminated frozen berries have been frequently identified as cause of foodborne disease outbreaks. To provide new tools for virus detection and characterization in berries, next generation sequencing (NGS) and reverse transcription-digital PCR (RT-dPCR) techniques were tested here with strawberries previously involved in a large-scale norovirus (NoV) gastroenteritis outbreak in Germany. By NGS, about 29 million sequence reads were generated, which mainly showed identities to sequences from the plant matrix and from the bacterial flora. Most abundant virus sequences originated from plant-specific viruses, whereas sequences with high identity to human viruses were rare. Only two sequence reads showed homologies to human NoV. They were identical to GII.P16/GII.13 NoV sequences from patients and a strawberry sample independently analyzed during the outbreak. Quantification of the GII NoV RNA of the berries using RT-dPCR confirmed a low mean virus amount of 185 copies/25 g, which is similar to independently assessed RT-qPCR results (257 copies/25 g). The study shows that identification of human-pathogenic viruses in naturally contaminated frozen berries is possible using NGS technologies. However, the method needs to be further optimized in order to enable convenient and reproducible detection of a low amount of human-pathogenic virus sequences in a background of highly abundant nucleic acids of other sources.

摘要

受病毒污染的冷冻浆果已被频繁认定为食源性疾病暴发的原因。为了在浆果中提供病毒检测和特征描述的新工具,本研究中使用下一代测序(NGS)和反转录数字 PCR(RT-dPCR)技术对先前涉及德国大规模诺如病毒(NoV)胃肠炎暴发的草莓进行了测试。通过 NGS 生成了约 2900 万条序列,这些序列主要与植物基质和细菌菌群的序列具有同源性。最丰富的病毒序列来源于植物特异性病毒,而与人类病毒具有高度同源性的序列则很少见。只有两条序列与人类 NoV 具有同源性。它们与患者的 GII.P16/GII.13 NoV 序列以及在暴发期间独立分析的草莓样本完全相同。使用 RT-dPCR 对浆果中的 GII NoV RNA 进行定量,证实了病毒含量的平均值为 185 拷贝/25g,与独立评估的 RT-qPCR 结果(257 拷贝/25g)相似。该研究表明,使用 NGS 技术可以鉴定出天然污染的冷冻浆果中的人类致病性病毒。然而,该方法需要进一步优化,以便能够在其他来源的高度丰富核酸背景下,方便且可重复地检测到低量的人类致病性病毒序列。

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