Chen J, Zheng H-Y, Antoniw J F, Adams M J, Chen J-P, Lin L
Virology and Biotechnology Department, Zhejiang Academy of Agricultural Sciences, Hangzhou, P.R., China.
Arch Virol. 2004 Mar;149(3):435-45. doi: 10.1007/s00705-003-0234-2. Epub 2003 Nov 13.
Degenerate primers for RT-PCR were designed and used to amplify genome fragments ( c. 750 nt in the coat protein-ORF6 region) of allexiviruses from a total of 28 garlic samples from 24 provinces in China. Many samples contained more than one distinct sequence. A total of 60 different sequences were obtained. Phylogenetic analysis and two-way comparisons were used to assess the status of the sequences and to re-examine the criteria for distinguishing species within the genus. Most of the sequences could be allocated to either Garlic virus D or Garlic virus X on the basis of sequence similarity but some appeared to be intermediate between existing species. There were no sequences of Garlic virus C or Shallot virus X. A comparison with the related genera Carlavirus, Foveavirus and Potexvirus suggests that the published allexivirus species demarcation criteria may have been drawn too tightly and should be re-examined.
设计了用于RT-PCR的简并引物,并用于从中国24个省份的总共28个大蒜样品中扩增蒜病毒属病毒的基因组片段(外壳蛋白-ORF6区域约750 nt)。许多样品包含不止一个不同的序列。总共获得了60个不同的序列。系统发育分析和双向比较用于评估序列的状态,并重新审视该属内区分物种的标准。根据序列相似性,大多数序列可归类为大蒜病毒D或大蒜病毒X,但有些序列似乎介于现有物种之间。没有大蒜病毒C或葱潜隐病毒X的序列。与相关属香石竹潜隐病毒属、凹顶病毒属和马铃薯X病毒属的比较表明,已发表的蒜病毒属物种划分标准可能定得过于严格,应重新审视。