Department of Plant Pathology, Nanjing Agricultural University, Jiangsu Province, China.
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Yunnan Agricultural University, Kunming, China.
PLoS Pathog. 2023 Apr 3;19(4):e1011301. doi: 10.1371/journal.ppat.1011301. eCollection 2023 Apr.
Cereal yellow dwarf virus (CYDV-RPV) encodes a P0 protein that functions as a viral suppressor of RNA silencing (VSR). The strength of silencing suppression is highly variable among CYDV-RPV isolates. In this study, comparison of the P0 sequences of CYDV-RPV isolates and mutational analysis identified a single C-terminal amino acid that influenced P0 RNA-silencing suppressor activity. A serine at position 247 was associated with strong suppressor activity, whereas a proline at position 247 was associated with weak suppressor activity. Amino acid changes at position 247 did not affect the interaction of P0 with SKP1 proteins from Hordeum vulgare (barley) or Nicotiana benthamiana. Subsequent studies found P0 proteins containing a P247 residue were less stable than the P0 proteins containing an S247 residue. Higher temperatures contributed to the lower stability and in planta and the P247 P0 proteins were subject to degradation via the autophagy-mediated pathway. A P247S amino acid residue substitution in P0 increased CYDV-RPV replication after expression in agroinfiltrated plant leaves and increased viral pathogenicity of P0 generated from the heterologous Potato virus X expression vector system. Moreover, an S247 CYDV-RPV could outcompete the P247 CYDV-RPV in a mixed infection in natural host at higher temperature. These traits contributed to increased transmission by aphid vectors and could play a significant role in virus competition in warming climates. Our findings underscore the capacity of a plant RNA virus to adapt to climate warming through minor genetic changes in gene-silencing suppressor, resulting in the potential for disease persistence and prevalence.
小麦黄花叶病毒(CYDV-RPV)编码的 P0 蛋白是一种作为病毒 RNA 沉默抑制剂(VSR)的功能蛋白。不同 CYDV-RPV 分离株的沉默抑制能力差异很大。在这项研究中,通过比较 CYDV-RPV 分离株的 P0 序列和突变分析,确定了一个单一的 C 末端氨基酸残基影响 P0 RNA 沉默抑制活性。位置 247 的丝氨酸与强抑制活性相关,而位置 247 的脯氨酸与弱抑制活性相关。位置 247 的氨基酸变化不影响 P0 与大麦 SKP1 蛋白或本氏烟 SKP1 蛋白的相互作用。随后的研究发现,含有 P247 残基的 P0 蛋白不如含有 S247 残基的 P0 蛋白稳定。较高的温度导致较低的稳定性,在植物体内,P247 的 P0 蛋白通过自噬介导的途径被降解。在 agroinfiltrated 植物叶片中表达后,P0 中的 P247S 氨基酸残基取代增加了 CYDV-RPV 的复制,并增加了来自异源马铃薯病毒 X 表达载体系统生成的 P0 的病毒致病性。此外,在较高温度的自然宿主中,混合感染中 P247 的 CYDV-RPV 可以与 P247 的 CYDV-RPV 竞争。这些特性有助于增加蚜虫载体的传播能力,并可能在气候变暖的情况下对病毒竞争产生重大影响。我们的研究结果强调了植物 RNA 病毒通过基因沉默抑制剂的微小遗传变化适应气候变暖的能力,从而导致疾病持续存在和流行的潜力。