Department of Plant Pathology, Irrigated Agriculture Research and Extensive Center, Washington State University, Prosser 99350, USA.
Phytopathology. 2010 Jul;100(7):698-707. doi: 10.1094/PHYTO-100-7-0698.
Genetic variability of field populations of Grapevine leafroll-associated virus 2 (GLRaV-2) in Pacific Northwest (PNW) vineyards was characterized by sequencing the entire coat protein (CP) and a portion of the heat-shock protein-70 homolog (HSP70h) genes. Phylogenetic analysis of CP and HSP70h nucleotide sequences obtained in this study and corresponding sequences from GenBank revealed segregation of GLRaV-2 isolates into six lineages with virus isolates from PNW distributed in 'PN', 'H4', and 'RG' lineages. An estimation of the ratio of nonsynonymous substitutions per nonsynonymous site to synonymous substitutions per synonymous site indicated that different selection pressures may be acting on the two genomic regions encoding proteins with distinct functions. Multiple alignments of CP amino acid sequences showed lineage-specific differences. Enzyme-linked immunosorbent assay results indicated that GLRaV-2-specific antibodies from a commercial source are unable to reliably detect GLRaV-2 isolates in the RG lineage, thereby limiting antibody-based diagnosis of all GLRaV-2 isolates currently found in PNW vineyards. A protocol based on reverse-transcription polymerase chain reaction and restriction fragment length polymorphism analysis was developed for differentiating GLRaV-2 isolates belonging to the three lineages present in the region. The taxonomic status of GLRaV-2 is discussed in light of the current knowledge of global genetic diversity of the virus.
葡萄卷叶伴随病毒 2(GLRaV-2)在太平洋西北地区(PNW)葡萄园田间种群的遗传变异通过测序整个外壳蛋白(CP)和部分热休克蛋白 70 同源物(HSP70h)基因来表征。本研究中获得的 CP 和 HSP70h 核苷酸序列以及来自 GenBank 的相应序列的系统发育分析表明,GLRaV-2 分离物分为六个谱系,来自 PNW 的病毒分离物分布在“PN”、“H4”和“RG”谱系中。非同义替换与同义替换比值的估计表明,两个编码具有不同功能蛋白质的基因组区域可能受到不同的选择压力。CP 氨基酸序列的多重比对显示出谱系特异性差异。酶联免疫吸附测定结果表明,商业来源的 GLRaV-2 特异性抗体无法可靠地检测 RG 谱系中的 GLRaV-2 分离物,从而限制了基于抗体的对目前在 PNW 葡萄园发现的所有 GLRaV-2 分离物的诊断。针对该地区存在的三个谱系的 GLRaV-2 分离物,开发了基于逆转录聚合酶链反应和限制性片段长度多态性分析的区分协议。根据目前对病毒全球遗传多样性的了解,讨论了 GLRaV-2 的分类地位。