首页> 外文期刊>Journal of Virological Methods >Whole genome sequence analysis of the arctic-lineage strain responsible for distemper in Italian wolves and dogs through a fast and robust next generation sequencing protocol.
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Whole genome sequence analysis of the arctic-lineage strain responsible for distemper in Italian wolves and dogs through a fast and robust next generation sequencing protocol.

机译:通过快速而强大的下一代测序方案,对引起意大利狼和犬瘟热的北极谱系菌株进行全基因组序列分析。

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Dynamic surveillance and characterization of canine distemper virus (CDV) circulating strains are essential against possible vaccine breakthroughs events. This study describes the setup of a fast and robust next-generation sequencing (NGS) Ion PGMTM protocol that was used to obtain the complete genome sequence of a CDV isolate (CDV2784/2013). CDV2784/2013 is the prototype of CDV strains responsible for severe clinical distemper in dogs and wolves in Italy during 2013. CDV2784/2013 was isolated on cell culture and total RNA was used for NGS sample preparation. A total of 112.3 Mb of reads were assembled de novo using MIRA version 4.0rc4, which yielded a total number of 403 contigs with 12.1% coverage. The whole genome (15,690 bp) was recovered successfully and compared to those of existing CDV whole genomes. CDV2784/2013 was shown to have 92% nt identity with the Onderstepoort vaccine strain. This study describes for the first time a fast and robust Ion PGMTM platform-based whole genome amplification protocol for non-segmented negative stranded RNA viruses starting from total cell-purified RNA. Additionally, this is the first study reporting the whole genome analysis of an Arctic lineage strain that is known to circulate widely in Europe, Asia and USA.
机译:犬瘟热病毒(CDV)循环株的动态监视和表征对于可能的疫苗突破事件至关重要。这项研究描述了快速,可靠的下一代测序(NGS)离子PGM TM 协议的设置,该协议用于获得CDV分离株的完整基因组序列(CDV2784 / 2013)。 CDV2784 / 2013是在2013年期间造成意大利犬和狼严重临床不适的CDV毒株的原型。通过细胞培养分离出CDV2784 / 2013,总RNA用于NGS样品制备。使用MIRA版本4.0rc4从头开始总共组装了112.3 Mb的读段,产生了总计403个重叠群,覆盖率达12.1%。成功地回收了整个基因组(15,690 bp),并与现有的CDV完整基因组进行了比较。已显示CDV2784 / 2013与Onderstepoort疫苗株具有92%nt的同一性。这项研究首次描述了一种快速,可靠的基于Ion PGM TM 平台的全基因组扩增方案,用于从总细胞纯化的RNA开始的非分段负链RNA病毒。此外,这是第一项报道了北极谱系菌株的全基因组分析的研究,该菌株在欧洲,亚洲和美国广泛流行。

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