Department of Biochemistry, The University of Stellenbosch, Private Bag X1, Stellenbosch, South Africa.
Arch Virol. 2009;154(12):1891-900. doi: 10.1007/s00705-009-0525-3. Epub 2009 Oct 28.
The coat protein (CP) gene of 75 South African Potato virus Y (PVY) isolates was amplified using reverse-transcriptase polymerase chain reaction (RT-PCR). The resulting cDNA products were cloned and sequenced. These sequences were used to identify the strains to which the isolates belonged. Some, when compared to reference sequences, belonged to the PVY(N) and PVY(O) strains. A number of isolates were found to demonstrate significant homology to PVY(N) strains from China. A large number of South African isolates possessed CP sequences showing evidence of recombination between PVY(N) and PVY(O) strains, similar to those of PVY(NTN) isolates. Multiplex RT-PCR analysis allowed further differentiation of PVY(O) isolates and revealed that the majority were of the PVY(N)-Wilga strain. It was deduced that the most likely way in which these isolates reached South Africa was via the importation of infected material.
使用逆转录聚合酶链反应(RT-PCR)扩增了 75 个南非马铃薯 Y 病毒(PVY)分离株的外壳蛋白(CP)基因。对所得 cDNA 产物进行克隆和测序。利用这些序列确定了分离株所属的菌株。其中一些与参考序列相比,属于 PVY(N)和 PVY(O)株。发现一些分离株与来自中国的 PVY(N)株具有显著同源性。大量南非分离株的 CP 序列显示出与 PVY(N)和 PVY(O)株之间重组的证据,类似于 PVY(NTN)分离株。多重 RT-PCR 分析进一步区分了 PVY(O)分离株,结果表明大多数为 PVY(N)-Wilga 株。据推断,这些分离株到达南非的最有可能的方式是通过进口受感染的材料。