Fakhfakh H, Vilaine F, Makni M, Robaglia C
Laboratoire de Génétique, Université de Tunis, Tunisia.
J Gen Virol. 1996 Mar;77 ( Pt 3):519-23. doi: 10.1099/0022-1317-77-3-519.
Potato virus Y (PVY) full-length cDNA has been found to be refractory to cloning in Escherichia coli cells. A full-length 9.7 kb PVY cDNA was obtained by reverse transcription polymerase chain reaction (RT-PCR) from the RNA of PVY (tuber necrotic strain, PVYNTN). Double-stranded DNA fragments were used as primers (ds megaprimers), to include signals for transcription in vivo (a cauliflower mosaic virus 35S RNA promoter and a nopaline synthase terminator) in the final PCR product. Biolistic bombardment with a helium particle gun was used to inoculate the amplified product to detached tobacco leaves. Inoculation of tobacco plants with ground inoculated leaves followed by northern blot, ELISA and immuno-electron microscopy demonstrated that the DNA was highly infectious with up to 90% of bombarded leaves containing the virus. This methodology will allow the use of reverse genetics in the study of PVY-plant interactions and will also be useful for obtaining infectious cDNA from other viruses with large RNA genomes.
马铃薯Y病毒(PVY)全长cDNA已被发现难以在大肠杆菌细胞中克隆。通过逆转录聚合酶链反应(RT-PCR)从PVY(块茎坏死株系,PVYNTN)的RNA中获得了一条9.7 kb的全长PVY cDNA。双链DNA片段用作引物(双链大引物),以便在最终的PCR产物中包含体内转录信号(花椰菜花叶病毒35S RNA启动子和胭脂碱合酶终止子)。使用氦粒子枪进行生物弹道轰击,将扩增产物接种到离体烟草叶片上。用研磨接种的叶片接种烟草植株,随后进行Northern印迹、ELISA和免疫电子显微镜检测,结果表明该DNA具有高度传染性,高达90%的轰击叶片含有该病毒。这种方法将允许在PVY与植物相互作用的研究中使用反向遗传学,也将有助于从其他具有大RNA基因组的病毒中获得感染性cDNA。