Digiaro M, Yahyaoui E, Martelli G P, Elbeaino T
Istituto Agronomico Mediterraneo di Bari, Via Ceglie 9, 70010, Valenzano, Bari, Italy.
Virus Genes. 2015 Feb;50(1):165-71. doi: 10.1007/s11262-014-1094-4. Epub 2014 Oct 15.
The complete genome of a Tomato black ring virus isolate (TBRV-Mirs) (RNA1, 7,366 nt and RNA2, 4,640 nt) and the RNA2 sequences (4,437; 4,445; and 4,442 nts) of three Grapevine chrome mosaic virus isolates (GCMV-H6, -H15, and -H27) were determined. All RNAs contained a single open reading frame encoding polyproteins of 254 kDa (p1) and 149 kDa (p2) for TBRV-Mirs RNA1 and RNA2, respectively, and 146 kDa for GCMV RNA2. p1 of TBRV-Mirs showed the highest identity with TBRV-MJ (94 %), Beet ringspot virus (BRSV, 82 %), and Grapevine Anatolian ringspot virus (GARSV, 66 %), while p2 showed the highest identity with TBRV isolates MJ (89 %) and ED (85 %), followed by BRSV (65 %), GCMV (58 %), and GARSV (57 %). The amino acid identity of RNA2 sequences of four GCMV isolates (three from this study and one from GenBank) ranged from 91 to 98 %, the homing protein being the most variable. The RDP3 program predicted putative intra-species recombination events for GCMV-H6 and recognized GCMV as a putative inter-species recombinant between GARSV and TBRV. In both cases, the recombination events were at the movement protein level.
测定了番茄黑环病毒分离株(TBRV-Mirs)的完整基因组(RNA1,7366个核苷酸;RNA2,4640个核苷酸)以及三种葡萄铬花叶病毒分离株(GCMV-H6、-H15和-H27)的RNA2序列(4437、4445和4442个核苷酸)。所有RNA均包含一个单一的开放阅读框,分别编码TBRV-Mirs RNA1和RNA2的254 kDa多聚蛋白(p1)和149 kDa多聚蛋白(p2),以及GCMV RNA2的146 kDa多聚蛋白。TBRV-Mirs的p1与TBRV-MJ(94%)、甜菜环斑病毒(BRSV,82%)和葡萄安纳托利亚环斑病毒(GARSV,66%)具有最高的同一性,而p2与TBRV分离株MJ(89%)和ED(85%)具有最高的同一性,其次是BRSV(65%)、GCMV(58%)和GARSV(57%)。四种GCMV分离株(本研究中的三种和GenBank中的一种)的RNA2序列的氨基酸同一性在91%至98%之间,归巢蛋白是变化最大的。RDP3程序预测了GCMV-H6可能的种内重组事件,并将GCMV识别为GARSV和TBRV之间可能的种间重组体。在这两种情况下,重组事件都发生在运动蛋白水平。