1Division of Agro-Environmental Research, Hokkaido Agricultural Research Center, NARO, Hitsujigaoka, Toyohira, Sapporo, Hokkaido 062-8555, Japan.
2NARO Headquarters, 3-1-1 Kannondai, Tsukuba, Ibaraki 305-8517, Japan.
Phytopathology. 2019 Aug;109(8):1475-1480. doi: 10.1094/PHYTO-11-18-0438-R. Epub 2019 Jun 12.
Wheat yellow mosaic virus (WYMV) belongs to the genus in the family and has a bipartite genome (RNA1 and RNA2). WYMV in Japan is classified into three pathotypes (I to III) based on its pathogenicity to wheat cultivars. Among these three, pathotypes I and II are discriminated by their pathogenicity to the wheat cultivar Fukuho; pathotype I infects Fukuho but pathotype II does not. In the present study, the genomic regions that are involved in such pathogenicity were examined using infectious viral cDNA clones of pathotypes I and II. Reassortant experiments between viral RNA1 and RNA2 revealed the presence of a viral factor related to pathogenicity in RNA1. A chimeric pathotype II virus harboring a cylindrical inclusion (CI) cistron from pathotype I facilitated systemic infection of Fukuho, indicating that CI protein is involved in pathogenicity. Furthermore, analysis of chimeric and site-directed mutants revealed that three amino acids at the N-terminal region of CI protein were involved in pathogenicity to Fukuho. On the other hand, at the single-cell level, pathotype II replicated in protoplasts of Fukuho similar to that of pathotype I virus. These data suggest that differential pathogenicity between pathotypes I and II was considered to depend on the ability of cell-to-cell or long-distance viral movement, in which CI protein is involved. To the best of our knowledge, this is the first report to show the involvement of the bymoviral CI protein in pathogenicity.
小麦黄花叶病毒(WYMV)属于 科 属,具有二分体基因组(RNA1 和 RNA2)。日本的 WYMV 根据其对小麦品种的致病性分为三个株系(I 至 III)。在这三个株系中,株系 I 和 II 通过其对小麦品种福穗的致病性来区分;株系 I 感染福穗,但株系 II 不感染。在本研究中,使用 I 型和 II 型的传染性病毒 cDNA 克隆检查了与这种致病性相关的基因组区域。RNA1 和 RNA2 之间的重组实验揭示了 RNA1 中存在与致病性相关的病毒因子。携带来自株系 I 的圆柱形内含子(CI)顺式元件的嵌合株系 II 病毒促进了福穗的系统感染,表明 CI 蛋白参与了致病性。此外,嵌合和定点突变分析表明,CI 蛋白的 N 端区域的三个氨基酸参与了对福穗的致病性。另一方面,在单细胞水平上,株系 II 类似于株系 I 病毒在福穗原代细胞中的复制。这些数据表明,株系 I 和 II 之间的差异致病性被认为取决于细胞间或长距离病毒运动的能力,其中 CI 蛋白参与其中。据我们所知,这是第一个报道表明 BYMOV CI 蛋白参与致病性的报告。