Al Rwahnih M, Uyemoto J K, Falk B W, Rowhani A
Department of Plant Pathology, University of California, Davis, CA 95616, USA.
Arch Virol. 2007;152(12):2197-206. doi: 10.1007/s00705-007-1064-4. Epub 2007 Sep 21.
The complete RNA genome of plum bark necrosis stem pitting-associated virus (PBNSPaV) was cloned and sequenced and was determined to be 14, 214 nts long. The genome structure revealed seven major open reading frames (ORFs), and nontranslated regions at the 5' and 3' ends. PBNSPaV represents the simplest genome organization in the genus Ampelovirus, family Closteroviridae. The ORFs 1a and 1b encode, respectively, a large polyprotein with a molecular mass (Mr) of 259.6 kDa containing conserved domains characteristic of a papain-like protease, methyltransferase and helicase (ORF1a) and a 64.1-kDa protein of eight conserved motifs characteristic of viral RNA-dependent RNA polymerase (RdRp) (ORF1b). ORF1b is presumably expressed via a +1 ribosomal frameshift mechanism. ORF2 encodes a small 6.3-kDa hydrophobic protein of unknown function. ORF3 encodes a 57.4-kDa protein, a homologue of the HSP70 family of heat shock proteins. ORF4 encodes a 61.6-kDa protein with unknown function. ORF5 encodes a 35.9-kDa capsid protein (CP). Lastly, ORF6 encodes a 25.2-kDa minor capsid protein (CPm). Phylogenetic analyses performed on sequences of the HSP70h RdRp and CP support classification of the virus in the genus Ampelovirus. A real-time TaqMan RT-PCR assay and a one-step RT-PCR were developed for PBNSPaV detection and compared using three different sample preparation methods.
李树皮坏死茎痘相关病毒(PBNSPaV)的完整RNA基因组被克隆并测序,其长度为14214个核苷酸。基因组结构显示有七个主要开放阅读框(ORF)以及5'和3'端的非翻译区。PBNSPaV代表了纤毛病毒科葡萄病毒属中最简单的基因组结构。ORF1a和ORF1b分别编码一个分子量(Mr)为259.6 kDa的大的多蛋白,该多蛋白含有木瓜蛋白酶样蛋白酶、甲基转移酶和解旋酶的保守结构域(ORF1a),以及一个具有病毒RNA依赖性RNA聚合酶(RdRp)八个保守基序的64.1 kDa蛋白(ORF1b)。ORF1b可能通过+1核糖体移码机制表达。ORF2编码一个功能未知的6.3 kDa小疏水蛋白。ORF3编码一个57.4 kDa的蛋白,它是热休克蛋白HSP70家族的同源物。ORF4编码一个功能未知的61.6 kDa蛋白。ORF5编码一个35.9 kDa的衣壳蛋白(CP)。最后,ORF6编码一个25.2 kDa的次要衣壳蛋白(CPm)。基于HSP70h、RdRp和CP序列进行的系统发育分析支持将该病毒归类于葡萄病毒属。开发了一种实时TaqMan RT-PCR检测方法和一步法RT-PCR用于PBNSPaV检测,并使用三种不同的样品制备方法进行了比较。