Donda Bhanu Priya, Jarugula Sridhar, Naidu Rayapati A
Department of Plant Pathology, Washington State University, Irrigated Agriculture Research and Extension Center, Prosser, WA 99350.
Phytopathology. 2017 Sep;107(9):1069-1079. doi: 10.1094/PHYTO-02-17-0061-R. Epub 2017 Jul 7.
Despite being the first closterovirus documented in grapevines (Vitis sp.), the molecular biology of Grapevine leafroll-associated virus 1 (GLRaV-1, genus Ampelovirus, family Closteroviridae) is still in its infancy. In this study, the complete genome sequence of two GLRaV-1 isolates was determined to be 18,731 (isolate WA-CH) and 18,946 (isolate WA-PN) nucleotides (nt). The genome of WA-CH and WA-PN isolates encodes nine putative open reading frames (ORFs) and the arrangement of these ORFs in both isolates was similar to that of Australian and Canadian isolates. In addition to two divergent copies of the coat protein (CP), the genome of GLRaV-1 isolates contain CP-homologous domain in four genes, making the virus unique among Closteroviridae members. The 5' and 3' nontranslated regions (NTRs) of WA-CH and WA-PN isolates showed differences in size and sequence composition, with 5' NTR having variable number of ∼65-nt-long repeats. Using the 5' NTR sequences, a reverse transcription-polymerase chain reaction and restriction fragment length polymorphism method was developed to distinguish GLRaV-1 variants in vineyards. Northern analysis of total RNA from GLRaV-1-infected grapevine samples revealed three subgenomic RNAs (sgRNAs), corresponding tentatively to CP, p21, and p24 ORFs, present at higher levels, with p24 sgRNA observed at relatively higher abundance than the other two sgRNAs. The 5' terminus of sgRNAs corresponding to CP, CPd1, CPd2, p21, and p24 were mapped to the virus genome and the leader sequence for these five sgRNAs determined to be 68, 27, 15, 49, and 18 nt, respectively. Taken together, this study provided a foundation for further elucidation of the comparative molecular biology of closteroviruses infecting grapevines.
尽管葡萄卷叶相关病毒1(GLRaV-1,属于黄症病毒属,长线形病毒科)是在葡萄(葡萄属)中记录的第一种长线形病毒,但其分子生物学仍处于起步阶段。在本研究中,两个GLRaV-1分离株的完整基因组序列被确定为18,731个核苷酸(分离株WA-CH)和18,946个核苷酸(分离株WA-PN)。WA-CH和WA-PN分离株的基因组编码九个推定的开放阅读框(ORF),并且这两个分离株中这些ORF的排列与澳大利亚和加拿大分离株的排列相似。除了两个不同的外壳蛋白(CP)拷贝外,GLRaV-1分离株的基因组在四个基因中含有CP同源结构域,这使得该病毒在长线形病毒科成员中独一无二。WA-CH和WA-PN分离株的5'和3'非翻译区(NTR)在大小和序列组成上存在差异,5'NTR具有可变数量的约65个核苷酸长的重复序列。利用5'NTR序列,开发了一种逆转录-聚合酶链反应和限制性片段长度多态性方法来区分葡萄园中的GLRaV-1变体。对来自感染GLRaV-1的葡萄样品的总RNA进行Northern分析,发现三个亚基因组RNA(sgRNA),初步对应于CP、p21和p24 ORF,含量较高,其中p24 sgRNA的丰度相对高于其他两个sgRNA。对应于CP、CPd1、CPd2、p21和p24的sgRNA的5'末端被定位到病毒基因组,并且确定这五个sgRNA的前导序列分别为68、27、15、49和18个核苷酸。总之,本研究为进一步阐明感染葡萄的长线形病毒的比较分子生物学提供了基础。