Sumi S, Tsuneyoshi T, Furutani H
Institute for Biotechnology Research, Wakunaga Pharmaceutical Co. Ltd., Hiroshima, Japan.
J Gen Virol. 1993 Sep;74 ( Pt 9):1879-85. doi: 10.1099/0022-1317-74-9-1879.
Rod-shaped flexuous viruses were partially purified from garlic plants (Allium sativum) showing typical mosaic symptoms. The genome was shown to be composed of RNA with a poly(A) tail of an estimated size of 10 kb as shown by denaturing agarose gel electrophoresis. We constructed cDNA libraries and screened four independent clones, which were designated GV-A, GV-B, GV-C and GV-D, using Northern and Southern blot hybridization. Nucleotide sequence determination of the cDNAs, two of which correspond to nearly one-third of the virus genomic RNA, shows that all of these viruses possess an identical genomic structure and that also at least four proteins are encoded in the viral cDNA, their M(r)s being estimated to be 15K, 27K, 40K and 11K. The 15K open reading frame (ORF) encodes the core-like sequence of a zinc finger protein preceded by a cluster of basic amino acid residues. The 27K ORF probably encodes the viral coat protein (CP), based on both the existence of some conserved sequences observed in many other rod-shaped or flexuous virus CPs and an overall amino acid sequence similarity to potexvirus and carlavirus CPs. The 11K ORF shows significant amino acid sequence similarities to the corresponding 12K proteins of the potexviruses and carlaviruses. On the other hand, the 40K ORF product does not resemble any other plant virus gene products reported so far. The genomic organization in the 3' region of the garlic viruses resembles, but clearly differs from, that of carlaviruses. Phylogenetic analysis based upon the amino acid sequence of the viral capsid protein also indicates that the garlic viruses have a unique and distinct domain different from those of the potexvirus and carlavirus groups. The results suggest that the garlic viruses described here belong to an unclassified and new virus group closely related to the carlaviruses.
从表现出典型花叶症状的大蒜植株(葱属植物)中部分纯化出杆状弯曲病毒。变性琼脂糖凝胶电泳显示,该病毒基因组由带有聚腺苷酸尾巴的RNA组成,估计大小为10kb。我们构建了cDNA文库,并使用Northern和Southern印迹杂交筛选出四个独立克隆,分别命名为GV-A、GV-B、GV-C和GV-D。对cDNA进行核苷酸序列测定,其中两个cDNA对应病毒基因组RNA的近三分之一,结果表明所有这些病毒都具有相同的基因组结构,并且病毒cDNA中至少编码四种蛋白质,其分子量估计分别为15K、27K、40K和11K。15K开放阅读框(ORF)编码一个锌指蛋白的核心样序列,其前面是一串碱性氨基酸残基。基于在许多其他杆状或弯曲病毒衣壳蛋白中观察到的一些保守序列以及与马铃薯X病毒属和香石竹潜隐病毒属衣壳蛋白的整体氨基酸序列相似性,27K ORF可能编码病毒衣壳蛋白(CP)。11K ORF与马铃薯X病毒属和香石竹潜隐病毒属相应的12K蛋白具有显著的氨基酸序列相似性。另一方面,40K ORF产物与迄今报道的任何其他植物病毒基因产物都不相似。大蒜病毒3'区域的基因组组织与香石竹潜隐病毒属相似,但明显不同。基于病毒衣壳蛋白氨基酸序列的系统发育分析也表明,大蒜病毒具有一个与马铃薯X病毒属和香石竹潜隐病毒属不同的独特区域。结果表明,这里描述的大蒜病毒属于一个未分类的新病毒组,与香石竹潜隐病毒属密切相关。