Janzac B, Tribodet M, Lacroix C, Moury B, Verrier J L, Jacquot E
INRA-Agrocampus Ouest-Université Rennes 1, UMR 1349 IGEPP, F-35653 Le Rheu, France; Imperial Tobacco Group, SEITA, Institut du Tabac, Domaine de la Tour, F-24100 Bergerac France; and INRA-Cirad Montpellier SupAgro, UMR 385 BGPI, Cirad TA A-54K, Campus International de Baillarguet, F-34398 Montpellier, France.
INRA-Agrocampus Ouest-Université Rennes 1.
Plant Dis. 2014 Nov;98(11):1521-1529. doi: 10.1094/PDIS-11-13-1126-RE.
Emergence of viral genotypes can make control strategies based on resistance genes ineffective. A few years after the deployment of tobacco genotypes carrying alleles of the Potato virus Y (PVY) recessive resistance gene va, virulent PVY isolates have been reported, suggesting the low durability of va. To have a broader view of the evolutionary processes involved in PVY adaptation to va, we studied mutational pathways leading to the emergence of PVY resistance-breaking populations. The viral genome-linked protein (VPg) has been described to be potentially involved in va adaptation. Analyses of the VPg sequence of PVY isolates sampled from susceptible and resistant tobacco allowed us to identify mutations in the central part of the VPg. Analysis of the virulence of wild-type isolates with known VPg sequences and of mutated versions of PVY infectious clones allowed us to (i) validate VPg as the PVY virulence factor corresponding to va, (ii) highlight the fact that virulence gain in PVY occurs rapidly and preferentially by substitution at position AA in the VPg, and (iii) show that the 101G substitution in the VPg of a PVY isolate is responsible for cross-virulence toward two resistance sources. Moreover, it appears that the evolutionary pathway of PVY adaptation to va depends on both virus and host genetic backgrounds.
病毒基因型的出现会使基于抗性基因的防治策略失效。在携带马铃薯Y病毒(PVY)隐性抗性基因va等位基因的烟草基因型被应用几年后,有报道称出现了毒性PVY分离株,这表明va的持久性较低。为了更全面地了解PVY适应va所涉及的进化过程,我们研究了导致PVY抗性突破群体出现的突变途径。病毒基因组连接蛋白(VPg)已被描述为可能参与va的适应过程。对从感病和抗病烟草中采集的PVY分离株的VPg序列进行分析,使我们能够鉴定出VPg中部的突变。对具有已知VPg序列的野生型分离株和PVY感染性克隆的突变版本的毒力分析,使我们能够(i)验证VPg是与va相对应的PVY毒力因子,(ii)强调PVY毒力增加迅速且优先通过VPg中AA位置的替换发生这一事实,以及(iii)表明PVY分离株VPg中的101G替换导致对两种抗性来源的交叉毒力。此外,似乎PVY适应va的进化途径取决于病毒和宿主的遗传背景。