Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia.
Aristotle University of Thessaloniki, School of Agriculture, Forestry and Natural Environment, Faculty of Agriculture, Plant Pathology Lab, Thessaloniki 54124, Greece.
Plant Dis. 2018 Feb;102(2):318-326. doi: 10.1094/PDIS-03-17-0418-RE. Epub 2017 Nov 21.
During the growing seasons of 2014 through 2016, a total of 336 leaf samples from bell pepper (showing leafroll and interveinal yellowing) and arable weeds were collected from Riyadh region, Saudi Arabia. The use of a polerovirus generic reverse transcription (RT)-PCR assay confirmed their presence in the bell pepper samples. Sequencing of the generic amplicon revealed high similarity (87.6 to 98.1% in nt) with four poleroviruses; Tobacco vein distorting virus, Pepper vein yellows virus, Pepper yellows virus, and Pepper yellow leaf curl virus. To further characterize one of these isolates (105D), a larger part of the genome (∼1,300 nt) spanning approximately from the 3' end of ORF2 to the middle of ORF3, was amplified and sequenced. Blasting the resulting sequence revealed the low amino acid and nucleotide identity percentages in the coat protein and movement protein partial genes with viruses deposited in GenBank. Next-generation sequence was used to acquire a larger part of the genome, which resulted in the reconstruction of isolate 105D's partial genome (5,496 nt). Sequence similarity analysis revealed the presence of a divergent polerovirus isolate belonging to a new species that was tentatively named Pepper leafroll chlorosis virus (PeLRCV). Using a specific RT-PCR assay for this isolate confirmed the presence of this new viral species in the symptomatic peppers. Aphid transmission experiments showed that PeLRCV is vectored by Aphis gossypii and that it can infect at least five out of the 15 different plants species tested. Based on our findings, PeLRCV is a new member of genus Polerovirus in the family Luteoviridae.
在 2014 年至 2016 年的生长季节,从沙特阿拉伯利雅得地区共采集了 336 份辣椒(表现为卷叶和叶脉间黄化)和旱地杂草的叶片样本。使用马铃薯卷叶病毒属通用逆转录(RT)-PCR 检测法确认了这些样本中存在马铃薯卷叶病毒属病毒。通用扩增子的测序结果显示,与 4 种马铃薯卷叶病毒属病毒(烟草叶脉扭曲病毒、胡椒叶脉黄化病毒、胡椒黄斑驳病毒和胡椒黄卷叶病毒)具有高度相似性(核苷酸序列相似度为 87.6%至 98.1%)。为了进一步对这些分离株中的一个(105D)进行鉴定,扩增并测序了约 1300 个核苷酸长的更大基因组部分(大约从 ORF2 的 3'端到 ORF3 的中部)。对获得的序列进行 Blast 分析,发现衣壳蛋白和运动蛋白部分基因的氨基酸和核苷酸同一性百分比与 GenBank 中已注册的病毒较低。使用下一代测序技术获取了更大的基因组部分,从而重建了分离株 105D 的部分基因组(5496 个核苷酸)。序列相似性分析显示,存在一种属于新种的分化马铃薯卷叶病毒属病毒,暂命名为胡椒卷叶黄化病毒(PeLRCV)。针对该分离株的特异性 RT-PCR 检测法证实了在有症状的辣椒中存在这种新的病毒种。蚜虫传播实验表明,PeLRCV 由棉蚜传播,并且可以感染至少 15 种不同测试植物中的 5 种以上。基于我们的研究结果,PeLRCV 是 Luteoviridae 科马铃薯卷叶病毒属的一个新成员。