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Discovery and molecular characterization of a new cryptovirus dsRNA genome from Japanese persimmon through conventional cloning and high-throughput sequencing

机译:通过常规克隆和高通量测序从日本柿中发现新的隐病毒dsRNA基因组并进行分子表征

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Through the application of next generation sequencing, in synergy with conventional cloning of DOP-PCR fragments, two double-stranded RNA (dsRNA) molecules of about 1.5 kbp in size were isolated from leaf tissue of a Japanese persimmon (accession SSPI) from Apulia (southern Italy) showing veinlets necrosis. High-throughput sequencing allowed whole genome sequence assembly, yielding a 1,577 and a 1,491 bp contigs identified as dsRNA-1 and dsRNA-2 of a previously undescribed virus, provisionally named as Persimmon cryptic virus (PeCV). In silico analysis showed that both dsRNA fragments were monocistronic and comprised the RNA-dependent RNA polymerase (RdRp) and the capsid protein (CP) genes, respectively. Phylogenetic reconstruction revealed a close relationship of these dsRNAs with those of cryptoviruses described in woody and herbaceous hosts, recently gathered in genus Deltapartitivirus. Virus-specific primers for RT-PCR, designed in the CP cistron, detected viral RNAs also in symptomless persimmon trees sampled from the same geographical area of SSPI, thus proving that PeCV infection may be fairly common and presumably latent.
机译:通过应用下一代测序技术,与DOP-PCR片段的常规克隆协同作用,从日本普柿(登录号SSPI)的叶组织中分离了两个大小约为1.5 kbp的双链RNA(dsRNA)分子(意大利南部)显示小静脉坏死。高通量测序允许整个基因组序列组装,产生一个1,577和1,491 bp重叠群,被鉴定为先前未描述的病毒(暂时称为柿子隐性病毒(PeCV))的dsRNA-1和dsRNA-2。在计算机分析中,两个dsRNA片段均为单顺反子,分别包含RNA依赖性RNA聚合酶(RdRp)和衣壳蛋白(CP)基因。系统发育重建揭示了这些dsRNA与最近在Deltapartitivirus属中收集的木本和草本宿主中描述的隐病毒的密切相关。在CP顺反子中设计的用于RT-PCR的病毒特异性引物在从SSPI的同一地理区域采样的无症状柿树中也检测到病毒RNA,因此证明PeCV感染可能相当普遍并且可能是潜在的。

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