期刊
VIRUSES-BASEL
卷 9, 期 11, 页码 -出版社
MDPI AG
DOI: 10.3390/v9110332
关键词
infectious cDNA clone; agroinfection; yeast-E; coli-Agrobacterium shuttle vector; yeast homologous recombination; potyvirus; potato virus Y; rhabdovirus; sonchus yellow net virus
类别
资金
- China National Science Foundation [31470255, 31671996]
- YNTC [2017YN02, 2014YN02]
The availability of infectious full-length clone is indispensable for reverse genetics studies of virus biology, pathology and construction of viral vectors. However, for RNA viruses with large genome sizes or those exhibiting inherent cloning difficulties, procedure to generate biologically active complementary DNA (cDNA) clones can be time-consuming or technically challenging. Here we have constructed a yeast-Escherichia coli-Agrobacterium shuttle vector that enables highly efficient homologous recombination in yeast for assembly of Agrobacterium compatible plant virus clones. Using this vector, we show that infectious cDNA clones of a plant negative-stranded RNA virus, sonchus yellow net rhabdovirus, can be rapidly assembled. In addition, one-step assembly of infectious clones of potato virus Y in yeast, either with or without intron, was readily achieved from as many as eight overlapping DNA fragments. More importantly, the recovered yeast plasmids can be transformed directly into Agrobacterium for inoculation, thereby obviating the E. coli cloning steps and associated toxicity issues. This method is rapid, highly efficient and cost-effective and should be readily applicable to a broad range of plant viruses.
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