Akram Mohammad, Kumar Deepender, Kamaal Naimuddin
Division of Crop Protection, ICAR-Indian Institute of Pulses Research, Kanpur, 208024, India.
Arch Virol. 2024 Dec 11;170(1):7. doi: 10.1007/s00705-024-06203-3.
In India, plants from the non-cultivated, horticultural, and agricultural categories are commonly infected with various begomoviruses, most of which produce yellow mosaic, bright yellow mosaic, or curling symptoms on leaves. In this study, the complete genome of a new bipartite begomovirus causing yellow mosaic disease (YMD) in butterfly pea (Clitoria ternatea L.) was characterized using rolling-circle amplification followed by restriction digestion, cloning, and sequencing to obtain the full-length DNA-A (2727 nt) and DNA-B (2648 nt) sequences. The DNA-A and DNA-B components have a genome organization that is typical of the Old World bipartite begomoviruses, and the common regions (95 nt) of DNA-A and DNA-B share 91% nucleotide sequence identity, which is well above the threshold (>85%) for them to be considered cognate components. Both DNA molecules contain a begomovirus nonanucleotide motif, conserved iterons, and a putative stem-loop structure. The DNA-A of this virus was found to be most similar to that of Cajanus scarabaeoides yellow mosaic virus (CsYMV), with 82.61% nucleotide sequence identity, which is far below the species demarcation threshold (< 91%) for begomoviruses, whereas the DNA-B sequence showed the most similarity (77.16% identity) to that of Rhynchosia yellow mosaic virus (RhYMV). In phylogenetic analysis, both DNA-A and DNA-B were formed a clade with the corresponding genome segments of other YMD-causing begomoviruses. Based on these characteristics, this virus, for which the name "butterfly pea yellow mosaic virus" (BpYMV) is proposed, should be considered a member of a new species in the genus Begomovirus.
在印度,来自非栽培、园艺和农业类别的植物普遍感染了各种双生病毒,其中大多数会在叶片上产生黄色花叶、亮黄色花叶或卷曲症状。在本研究中,利用滚环扩增,随后进行限制性酶切、克隆和测序,对一种在蝶豆(Clitoria ternatea L.)上引起黄色花叶病(YMD)的新型双分体双生病毒的全基因组进行了表征,从而获得了全长DNA-A(2727 nt)和DNA-B(2648 nt)序列。DNA-A和DNA-B组分具有旧世界双分体双生病毒典型的基因组结构,DNA-A和DNA-B的共同区域(95 nt)具有91%的核苷酸序列同一性,远高于被视为同源组分的阈值(>85%)。两个DNA分子都含有双生病毒九核苷酸基序、保守的重复序列和一个假定的茎环结构。发现该病毒的DNA-A与木豆叶甲黄色花叶病毒(CsYMV)的DNA-A最为相似,核苷酸序列同一性为82.61%,远低于双生病毒的种间区分阈值(<91%),而DNA-B序列与长喙豆黄色花叶病毒(RhYMV)的DNA-B序列相似度最高(同一性为77.16%)。在系统发育分析中,DNA-A和DNA-B均与其他引起YMD的双生病毒的相应基因组片段形成一个分支。基于这些特征,这种病毒应被视为双生病毒属一个新物种的成员,为此提出了“蝶豆黄色花叶病毒”(BpYMV)这一名称。