National Key Laboratory of Agromicrobiology, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China.
Virus Res. 2013 Jan;171(1):15-21. doi: 10.1016/j.virusres.2012.10.014. Epub 2012 Oct 18.
Grapevine leafroll-associated virus 3 (GLRaV-3) is the most prevalent causal agent of grapevine leafroll disease (GLD). Of the 75 grapevine samples collected from three regions in China, 46.7% and 94.7% of samples tested positive for GLRaV-3 in reverse transcription-PCR (RT-PCR) and reverse transcription nested PCR (RT-nPCR), respectively. The SSCP analysis for the clones of complete CP gene from 16 GLRaV-3 isolates showed that 15 isolates contained one predominant haplotype and one isolate had no predominant haplotype. The sequences of the CP genes showed 89.9-100% identities at the nucleotide level. Phylogenetic analysis of the CP gene sequences revealed the existence of four well defined variant groups, which corresponded to previously reported phylogenetic groups (1, 2, 3, and 5). Two new sub-groups designated as sub-group 1B and sub-group 3B in groups 1 and 3, respectively, were identified in the Chinese GLRaV-3 population. Recombination analyses illustrated that those two new sub-groups (1B and 3B) were emerged as a result of recombination events between variants in groups 1 and 2, and variants in groups 1 and 3, respectively. These results further indicated that the variants in those new sub-groups are viable and evolutionary successful. Recombinants with highly similar coat protein structure to variants of group 1 were abundantly found in the viral population. In addition, these analyses provided evidence about CP gene as one of the recombination hotspots in GLRaV-3 genome. The population genetic parameters of all available CP sequences suggested that the recombinants might have emerged due to population bottlenecks during transmission. The results provide new insights into the variability and evolution of GLRaV-3.
葡萄扇叶病毒 3(GLRaV-3)是引起葡萄扇叶病(GLD)的最主要病原。在中国三个地区采集的 75 个葡萄样本中,46.7%和 94.7%的样本在逆转录-PCR(RT-PCR)和逆转录嵌套-PCR(RT-nPCR)中检测到 GLRaV-3 呈阳性。对 16 个 GLRaV-3 分离物完整 CP 基因克隆的 SSCP 分析表明,15 个分离物含有一个主要单倍型,而一个分离物没有主要单倍型。CP 基因序列在核苷酸水平上具有 89.9-100%的同一性。CP 基因序列的系统发育分析表明,存在四个明确的变异群,与先前报道的系统发育群(1、2、3 和 5)相对应。在中国 GLRaV-3 群体中,发现了两个新的亚群,分别命名为 1 群和 3 群的亚群 1B 和亚群 3B。重组分析表明,这两个新亚群(1B 和 3B)是由 1 群和 2 群之间以及 1 群和 3 群之间的变异重组产生的。这些结果进一步表明,这些新亚群中的变异是可行的,并且在进化上是成功的。在病毒群体中发现了大量与 1 群变体具有高度相似衣壳蛋白结构的重组体。此外,这些分析提供了证据表明 CP 基因是 GLRaV-3 基因组中的一个重组热点。所有可用 CP 序列的种群遗传参数表明,重组体可能是由于在传播过程中种群瓶颈而出现的。这些结果为 GLRaV-3 的变异性和进化提供了新的见解。