Rastgou Mina, Roumi Vahid, Noris Emanuela, Matić Slavica, Ercisli Sezai
Department of Plant Protection, Faculty of Agriculture, Urmia University, Urmia 5756151818, Iran.
Department of Plant Protection, College of Agriculture, University of Maragheh, Maragheh 5518183111, Iran.
Plants (Basel). 2022 Apr 20;11(9):1118. doi: 10.3390/plants11091118.
Grapevine virus A (GVA), the type species of the genus, is one of the causal agents of the Kober stem grooving disease of the rugose wood complex and one of the most frequently detected viruses in grapevine. There is little information on GVA gene(s) marker useful for phylogenetic analysis. To this aim, a total of 403 leaf samples were collected from vineyards of East and West Azarbaijan provinces in the Northwestern provinces of Iran during 2014-2016 and tested by DAS-ELISA and RT-PCR using ORF5-specific primers. GVA was detected in 56 symptomatic samples, corresponding to 14% of infection, while it was not detected in asymptomatic samples. The ORF5 (p10) protein sequence of eight Iranian isolates was compared to other vitiviruses, showing that the most conserved region resides in the N-terminus, carrying an arginine-rich motif followed by a zinc-finger motif. Next, to define a robust phylogenetic marker representative of the whole genome sequence suitable for phylogenetic and evolutionary studies, phylogenetic trees based on the full genome sequences of all the available GVA isolates and on individual genomic regions were constructed and compared. ORF1, which encodes the RNA-dependent RNA polymerase, was found to be the best phylogenetic marker for GVA classification and evolution studies. These results can be used for further research on phylogenetic analyses, evolution history, epidemiology, and etiology of rugose wood complex, and to identify control measures against GVA and other vitiviruses.
葡萄扇叶病毒A(GVA)是该属的模式种,是皱木复合病中柯贝茎沟病的致病因子之一,也是葡萄园中最常检测到的病毒之一。关于可用于系统发育分析的GVA基因标记的信息很少。为此,在2014年至2016年期间,从伊朗西北部东阿塞拜疆省和西阿塞拜疆省的葡萄园收集了总共403份叶片样本,并使用ORF5特异性引物通过双抗夹心酶联免疫吸附测定(DAS-ELISA)和逆转录聚合酶链反应(RT-PCR)进行检测。在56份有症状的样本中检测到了GVA,感染率为14%,而在无症状样本中未检测到。将8个伊朗分离株的ORF5(p10)蛋白序列与其他葡萄病毒进行了比较,结果表明最保守的区域位于N端,带有一个富含精氨酸的基序,后面跟着一个锌指基序。接下来,为了定义一个代表全基因组序列的强大系统发育标记物,适用于系统发育和进化研究,构建并比较了基于所有可用GVA分离株的全基因组序列和单个基因组区域的系统发育树。发现编码RNA依赖的RNA聚合酶的ORF1是用于GVA分类和进化研究的最佳系统发育标记物。这些结果可用于对皱木复合病的系统发育分析、进化历史、流行病学和病因学的进一步研究,并确定针对GVA和其他葡萄病毒的控制措施。