Nurkiyanova K M, Ryabov E V, Commandeur U, Duncan G H, Canto T, Gray S M, Mayo M A, Taliansky M E
Virology Department, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK.
J Gen Virol. 2000 Mar;81(Pt 3):617-26. doi: 10.1099/0022-1317-81-3-617.
A full-length cDNA corresponding to the RNA genome of Potato leafroll virus (PLRV) was modified by inserting cDNA that encoded the jellyfish green fluorescent protein (GFP) into the P5 gene near its 3' end. Nicotiana benthamiana protoplasts electroporated with plasmid DNA containing this cDNA behind the 35S RNA promoter of Cauliflower mosaic virus became infected with the recombinant virus (PLRV-GFP). Up to 5% of transfected protoplasts showed GFP-specific fluorescence. Progeny virus particles were morphologically indistinguishable from those of wild-type PLRV but, unlike PLRV particles, they bound to grids coated with antibodies to GFP. Aphids fed on extracts of these protoplasts transmitted PLRV-GFP to test plants, as shown by specific fluorescence in some vascular tissue and epidermal cells and subsequent systemic infection. In plants agroinfected with PLRV-GFP cDNA in pBIN19, some cells became fluorescent and systemic infections developed. However, after either type of inoculation, fluorescence was mostly restricted to single cells and the only PLRV genome detected in systemically infected tissues lacked some or all of the inserted GFP cDNA, apparently because of naturally occurring deletions. Thus, intact PLRV-GFP was unable to move from cell to cell. Nevertheless, PLRV-GFP has novel potential for exploring the initial stages of PLRV infection.
通过将编码水母绿色荧光蛋白(GFP)的cDNA插入马铃薯卷叶病毒(PLRV)RNA基因组3'端附近的P5基因中,对全长cDNA进行了修饰。用含有该cDNA的质粒DNA在花椰菜花叶病毒35S RNA启动子后进行电穿孔处理的本氏烟草原生质体被重组病毒(PLRV-GFP)感染。高达5%的转染原生质体显示出GFP特异性荧光。子代病毒粒子在形态上与野生型PLRV的病毒粒子无法区分,但与PLRV粒子不同的是,它们能与包被有抗GFP抗体的网格结合。取食这些原生质体提取物的蚜虫将PLRV-GFP传播到试验植物上,一些维管组织和表皮细胞中出现特异性荧光以及随后的系统感染证明了这一点。在pBIN19中用PLRV-GFP cDNA进行农杆菌介导感染的植物中,一些细胞发出荧光并发生了系统感染。然而,在任何一种接种方式后,荧光大多局限于单个细胞,并且在系统感染组织中检测到的唯一PLRV基因组缺少部分或全部插入的GFP cDNA,这显然是由于自然发生的缺失。因此,完整的PLRV-GFP无法在细胞间移动。尽管如此,PLRV-GFP在探索PLRV感染的初始阶段具有新的潜力。