Liu S, Bedford I D, Briddon R W, Markham P G
Department of Virus Research, John Innes Centre, Norwich, UK.
J Gen Virol. 1997 Jul;78 ( Pt 7):1791-4. doi: 10.1099/0022-1317-78-7-1791.
Clones of two subgroup III geminiviruses, the common strain of tomato golden mosaic virus (csTGMV) and African cassava mosaic virus originating from Kenya (ACMV-K), were shown to be non-transmissible by whitefiles. Lack of transmissibility of cloned ACMV-K was investigated by exchanging genomic components with a whitefly-transmissible ACMV isolate from Nigeria (ACMV-NOg). Neither pseudorecombinant was transmissible, indicating that defects in both genomic components contributed to the lack of transmissibility. Analysis of the acquisition of the pseudorecombinats by Bemisia tabaci indicated that accumulation of virus within the insect was DNA B dependent. Return of virus to plants was determined by DNA A, although the coat protein was essential for acquisition. Repeated passaging of both the wild strain of ACMV-NOg and the cloned virus led to loss of insect transmissibility of the wild isolate but not the cloned virus. Products encoded on both genomic components are required for transmission of bipartite geminiviruses by B. tabaci.
两种III亚组双生病毒的克隆体,番茄金色花叶病毒常见株系(csTGMV)和源自肯尼亚的非洲木薯花叶病毒(ACMV-K),被证明不能通过烟粉虱传播。通过将基因组组分与来自尼日利亚的烟粉虱可传播的ACMV分离株(ACMV-NOg)进行交换,研究了克隆的ACMV-K的不可传播性。两种假重组体均不可传播,这表明两个基因组组分中的缺陷都导致了不可传播性。对烟粉虱获取假重组体的分析表明,病毒在昆虫体内的积累依赖于DNA B。尽管外壳蛋白对于获取病毒至关重要,但病毒回到植物体内是由DNA A决定的。ACMV-NOg野生株系和克隆病毒的反复传代导致野生分离株失去昆虫传播性,但克隆病毒没有。双分体双生病毒通过烟粉虱传播需要两个基因组组分上编码的产物。