Revathy K A, Bhat A I
Division of Crop Protection, ICAR-Indian Institute of Spices Research, Marikunnu, Kozhikode, Kerala 673012 India.
University of Calicut, Malappuram, Kerala 673635 India.
Virusdisease. 2017 Sep;28(3):309-314. doi: 10.1007/s13337-017-0386-4. Epub 2017 Jun 17.
The complete genome of cucumber mosaic virus (CMV) from black pepper was sequenced and compared with CMV isolates from subgroups I and II reported worldwide. Percent identity and phylogenetic analyses clearly indicated that the CMV isolate from black pepper (BP) belongs to subgroup IB. Sequence analyses also showed the presence of a rare deletion of nine nucleotides in the putative methyltransferase domain of 1a gene which was observed only in two more isolates of CMV among one hundred 1a gene sequences of CMV for which sequence information is available in the database. Interestingly this deletion is not present in the black pepper isolate of CMV from China (WN1) and from Indian long pepper that is closely related to black pepper. Percent identity analyses showed that the 3'untranslated region (UTR) of the three RNAs of the BP isolate were conserved with 91% identity whereas the 5'UTR of three RNAs showed 52-80% identity. The level of gene conservation among the subgroups was highest in coat protein and lowest in 2b. The values of nucleotide diversity studies were further consistent with the above data. The ratio of non-synonymous to the synonymous substitution of the five genes of three RNAs was in the order 1a > 2a > 2b > 3a > 3b and less than one for all the genes, indicating purifying selection. These clearly reflect that the protein encoded by RNA1 is highly tolerant to amino acid changes followed by that of RNA2 and, RNA3 is the least tolerant correlating to its functional importance.
对来自黑胡椒的黄瓜花叶病毒(CMV)的全基因组进行了测序,并与全球报道的I组和II组CMV分离株进行了比较。百分比同一性和系统发育分析清楚地表明,来自黑胡椒(BP)的CMV分离株属于IB亚组。序列分析还显示,在1a基因的推定甲基转移酶结构域中存在9个核苷酸的罕见缺失,在数据库中可获得序列信息的100个CMV的1a基因序列中,仅在另外两个CMV分离株中观察到这种缺失。有趣的是,来自中国的CMV黑胡椒分离株(WN1)和与黑胡椒密切相关的印度长胡椒的CMV分离株中不存在这种缺失。百分比同一性分析表明,BP分离株的三个RNA的3'非翻译区(UTR)保守性为91%,而三个RNA的5'UTR的同一性为52-80%。亚组间基因保守水平在外壳蛋白中最高,在2b中最低。核苷酸多样性研究的值与上述数据进一步一致。三个RNA的五个基因的非同义替换与同义替换的比率顺序为1a > 2a > 2b > 3a > 3b,且所有基因的该比率均小于1,表明存在纯化选择。这些清楚地反映出,RNA1编码的蛋白质对氨基酸变化具有高度耐受性,其次是RNA2,而RNA3的耐受性最低,这与其功能重要性相关。