Wang Rong, Dong Jiali, Wang Zhen, Zhou Tao, Li Yong, Ding Wanlong
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 151 Malianwa North Road, Beijing, 100193, China.
Shandong Agricultural University, Tai'an, 271018, China.
Arch Virol. 2018 Jul;163(7):1973-1976. doi: 10.1007/s00705-018-3791-0. Epub 2018 Mar 10.
A new virus causing a serious stunt disease of chrysanthemum was identified in China by high-throughput sequencing (HTS) and named chrysanthemum virus R (CVR). The complete sequence of CVR was determined by reverse transcription polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE). The genomic RNA of CVR consists of 8,874 nucleotides (nt), excluding the poly(A) tail, contains six putative open reading frames (ORFs), and has a genomic organization typical of members of the genus Carlavirus. BLAST analysis of the full genome sequence showed low similarity (38%-56% sequence identity) to other members of the genus Carlavirus. BLAST analysis and phylogenetic analysis based on the amino acid (aa) sequences of the CVR replicase and coat protein (CP) confirmed that CVR is a distinct member of the genus Carlavirus.
通过高通量测序(HTS)在中国鉴定出一种导致菊花严重矮化病的新型病毒,并将其命名为菊花病毒R(CVR)。通过逆转录聚合酶链反应(RT-PCR)和cDNA末端快速扩增(RACE)确定了CVR的完整序列。CVR的基因组RNA由8874个核苷酸(nt)组成,不包括聚(A)尾,包含六个推定的开放阅读框(ORF),并且具有香石竹潜隐病毒属成员典型的基因组结构。对全基因组序列的BLAST分析显示,与香石竹潜隐病毒属的其他成员相似度较低(序列同一性为38%-56%)。基于CVR复制酶和外壳蛋白(CP)氨基酸(aa)序列的BLAST分析和系统发育分析证实,CVR是香石竹潜隐病毒属的一个独特成员。