Mitra Arunabha, Jarugula Sridhar, Naidu Rayapati A
Department of Plant Pathology, Washington State University, Irrigated Agriculture Research and Extension Center, Prosser, WA 99350, U.S.A.
Phytopathology. 2025 Aug;115(8):1065-1075. doi: 10.1094/PHYTO-12-24-0380-R. Epub 2025 Aug 6.
Grapevine leafroll-associated virus 1 (GLRaV-1, genus , family ) has a monopartite RNA genome with the size varying among genetic variants between 18,731 and 18,946 nucleotides (nt) and a 5' non-translated region (5'-NTR), varying in length between 857 and 922 nt. This study was undertaken to examine the role of the 5'-NTR in GLRaV-1 replication. For this purpose, a minireplicon cDNA clone, consisting of the 5'-NTR, the replicase gene module, the green fluorescent protein (GFP) reporter gene, and the 3'-NTR, was constructed. The functionality of the minireplicon was validated by GFP fluorescence and the presence of GFP-specific mRNA transcripts by Northern blot hybridization and reverse transcription quantitative PCR assays in leaves agro-coinfiltrated with silencing suppressors. The minireplicon retained functionality when its 5'-NTR was exchanged with corresponding sequences from distinct genetic variants of GLRaV-1. In contrast, the minireplicon of GLRaV-1 was nonfunctional when its 5'-NTR sequence was swapped with corresponding sequences from other GLRaV species. Deletion mutations in the 5'-NTR indicated that the first 32 nt at the 5'-terminus of the genome are essential for replication of the minireplicon. The in silico-predicted secondary structure of the 5'-terminal 32-nt sequence showed two stem-loop structures and mutations that altered these secondary structures or compensatory mutations preserving the secondary structures that failed to retain functionality of the minireplicon, suggesting that the nucleotide sequence, rather than any higher order secondary structures in this genomic region, is important for replication.
葡萄卷叶相关病毒1(GLRaV-1,属,科)具有单分体RNA基因组,其大小在不同遗传变体之间有所不同,介于18,731和18,946个核苷酸(nt)之间,5'非翻译区(5'-NTR)长度在857至922 nt之间变化。本研究旨在探讨5'-NTR在GLRaV-1复制中的作用。为此,构建了一个微型复制子cDNA克隆,其由5'-NTR、复制酶基因模块、绿色荧光蛋白(GFP)报告基因和3'-NTR组成。通过GFP荧光以及在与沉默抑制子进行农杆菌共浸润的叶片中通过Northern印迹杂交和逆转录定量PCR分析检测GFP特异性mRNA转录本的存在,验证了微型复制子的功能。当微型复制子的5'-NTR与GLRaV-1不同遗传变体的相应序列交换时,其仍保留功能。相反,当GLRaV-1微型复制子的5'-NTR序列与其他GLRaV物种的相应序列交换时,其无功能。5'-NTR中的缺失突变表明基因组5'末端的前32 nt对于微型复制子的复制至关重要。5'末端32 nt序列的计算机预测二级结构显示有两个茎环结构,改变这些二级结构的突变或保留二级结构但未能保留微型复制子功能的补偿性突变,表明该基因组区域中的核苷酸序列而非任何更高阶的二级结构对复制很重要。