Institute of Sugar Beet Research, Holtenser Landstr. 77, D-37079 Goettingen, Germany.
Phytopathology. 2011 Jun;101(6):718-24. doi: 10.1094/PHYTO-06-10-0157.
The genome of most Beet necrotic yellow vein virus (BNYVV) isolates is comprised of four RNAs. The ability of certain isolates to overcome Rz1-mediated resistance in sugar beet grown in the United States and Europe is associated with point mutations in the pathogenicity factor P25. When the virus is inoculated mechanically into sugar beet roots at high density, the ability depends on an alanine to valine substitution at P25 position 67. Increased aggressiveness is shown by BNYVV P type isolates, which carry an additional RNA species that encodes a second pathogenicity factor, P26. Direct comparison of aggressive isolates transmitted by the vector, Polymyxa betae, has been impossible due to varying population densities of the vector and other soilborne pathogens that interfere with BNYVV infection. Mechanical root inoculation and subsequent cultivation in soil that carried a virus-free P. betae population was used to load P. betae with three BNYVV isolates: a European A type isolate, an American A type isolate, and a P type isolate. Resistance tests demonstrated that changes in viral aggressiveness towards Rz1 cultivars were independent of the vector population. This method can be applied to the study of the synergism of BNYVV with other P. betae-transmitted viruses.
大多数甜菜坏死黄脉病毒(BNYVV)分离株的基因组由 4 个 RNA 组成。某些分离株能够克服在美国和欧洲种植的甜菜中 Rz1 介导的抗性,这与致病性因子 P25 中的点突变有关。当病毒以高浓度机械接种到甜菜根中时,这种能力取决于 P25 位置 67 处的丙氨酸到缬氨酸取代。BNYVV P 型分离株表现出更强的侵袭性,它们携带额外的 RNA 种类,编码第二个致病性因子 P26。由于载体 Polymyxa betae 的种群密度不同,以及其他干扰 BNYVV 感染的土传病原体,通过该载体传播的侵袭性分离株的直接比较是不可能的。使用机械根接种和随后在携带无病毒 P. betae 种群的土壤中进行的培养,将三种 BNYVV 分离株(一种欧洲 A 型分离株、一种美国 A 型分离株和一种 P 型分离株)加载到 P. betae 中。抗性测试表明,病毒对 Rz1 品种的侵袭性变化与载体种群无关。这种方法可应用于研究 BNYVV 与其他由 P. betae 传播的病毒的协同作用。