1Research Faculty of Agriculture, Hokkaido University, Sapporo 060-8589, Japan.
2Department of Entomology and Plant Pathology, University of Tennessee, Knoxville, TN 37996, U.S.A.
Mol Plant Microbe Interact. 2019 Aug;32(8):1026-1037. doi: 10.1094/MPMI-12-18-0331-R. Epub 2019 Jun 25.
Clover yellow vein virus (ClYVV) infects and causes disease in legume plants. However, here, we found that ClYVV isolate No. 30 (ClYVV-No.30) inefficiently multiplied or spread via cell-to-cell movement in mechanically inoculated leaves of a dozen soybean () cultivars and resulted in failure to spread systemically. Soybean plants also had a similar resistance phenotype against additional ClYVV isolates. In contrast, all but one of 24 tested accessions of wild soybeans () were susceptible to ClYVV-No.30. Graft inoculation of cultivated soybean TK780 with ClYVV-No.30-infected wild soybean B01167 scion resulted in systemic infection of the cultivated soybean rootstock. This suggests that, upon mechanical inoculation, the cultivated soybean inhibits ClYVV-No.30, at infection steps prior to the systemic spread of the virus, via vascular systems. Systemic infection of all F1 plants from crossing between TK780 and B01167 and of 68 of 76 F2 plants with ClYVV-No.30 indicated recessive inheritance of the resistance. Further genetic analysis using 64 recombinant inbred lines between TK780 and B01167 detected one major quantitative trait locus, designated , for the resistance that was positioned in the linkage group D1b (chromosome 2). The mapped region on soybean genome suggests that is not an allele of the known resistance genes against soybean mosaic virus.
三叶草黄脉病毒(ClYVV)感染并引起豆科植物发病。然而,在这里,我们发现 ClYVV 分离株 No.30(ClYVV-No.30)在通过机械接种的十几个大豆品种叶片中细胞间移动效率低或传播,导致无法系统传播。大豆植株对其他 ClYVV 分离株也表现出类似的抗性表型。相比之下,在 24 个测试的野生大豆品系中,只有一个对 ClYVV-No.30 敏感。将感染 ClYVV-No.30 的野生大豆 B01167 接穗嫁接到栽培大豆 TK780 上,导致栽培大豆砧木的系统性感染。这表明,在机械接种后,栽培大豆通过维管束系统在病毒系统传播之前的感染步骤中抑制 ClYVV-No.30。来自 TK780 和 B01167 杂交的所有 F1 植株以及携带 ClYVV-No.30 的 76 个 F2 植株中的 68 个均表现出系统感染,表明该抗性为隐性遗传。进一步使用 TK780 和 B01167 之间的 64 个重组自交系进行遗传分析,检测到一个主效数量性状基因座,命名为 ,该基因座定位在连锁群 D1b(染色体 2)上,与抗性有关。大豆基因组上的图谱区域表明, 不是已知抗大豆花叶病毒抗性基因的等位基因。