Balasubramanian V, Sukanya R S, Anuradha C, Selvarajan R
Molecular Virology Lab, Division of Crop Protection, National Research Centre for Banana, Thogamalai Road, Thayanur Post, Tiruchirapalli, 620102 Tamil Nadu India.
Virusdisease. 2014 Dec;25(4):460-6. doi: 10.1007/s13337-014-0241-9. Epub 2014 Nov 28.
Banana bract mosaic virus (BBrMV) is a serious constraint in the production of banana and plantain in India. In this study, we have cloned, sequenced and analyzed the helper component proteinase (HC-Pro) gene of 22 isolates from India and compared with previously reported BBrMV isolates. Sequence identity of BBrMV isolates encoding HC-Pro gene, were 92-100 % both at the nucleotide (nt) and amino acid level. Phylogenetic analysis based on nt sequences of non recombinant isolates showed that TN15, TN9 and TN24 formed one cluster and all the remaining isolates formed into another cluster. Different functional motifs in the central region of HC-Pro gene of BBrMV isolates were found conserved. Four potential recombinants with a total of 15 breakpoints were mostly observed at the N and a few from C terminal regions. The codon based selection analysis revealed that most of the codons were under purifying or negative selection except a codon at position 74 which was under positive selection. It is likely that recombination identified in Indian BBrMV isolates, along with strong purifying selection, enhances the speed of elimination of deleterious mutations in the HC-Pro gene. This study suggested that negative selection and recombination were important evolutionary factors driving the genetic diversification and population structure of Indian BBrMV isolates. To the best of our knowledge, this is the first report on the diversity analysis and occurrence of recombination in the HC-Pro gene of BBrMV.
香蕉苞片花叶病毒(BBrMV)是印度香蕉和大蕉生产中的一个严重制约因素。在本研究中,我们克隆、测序并分析了来自印度的22个分离株的辅助成分蛋白酶(HC-Pro)基因,并与先前报道的BBrMV分离株进行了比较。编码HC-Pro基因的BBrMV分离株在核苷酸(nt)和氨基酸水平上的序列同一性均为92%-100%。基于非重组分离株nt序列的系统发育分析表明,TN15、TN9和TN24形成一个簇,其余所有分离株形成另一个簇。发现BBrMV分离株HC-Pro基因中心区域的不同功能基序是保守的。总共15个断点的4个潜在重组体大多出现在N端,少数出现在C端区域。基于密码子的选择分析表明,除了第74位的一个密码子处于正选择外,大多数密码子处于纯化或负选择。印度BBrMV分离株中鉴定出的重组,连同强烈的纯化选择,可能会加快HC-Pro基因中有害突变的消除速度。本研究表明,负选择和重组是驱动印度BBrMV分离株遗传多样性和群体结构的重要进化因素。据我们所知,这是关于BBrMV的HC-Pro基因多样性分析和重组发生的首次报道。