Akram Mohammad, Kamaal Naimuddin, Kumar Deepender, Datta Dibendu, Agnihotri Aniruddha Kumar
Division of Crop Protection, ICAR-Indian Institute of Pulses Research, Kalyanpur, Kanpur, 208024, India.
Division of Crop Improvement, ICAR-Indian Institute of Pulses Research, Kalyanpur, Kanpur, 208024, India.
Virus Genes. 2025 Feb;61(1):110-120. doi: 10.1007/s11262-024-02120-4. Epub 2024 Nov 6.
Rhynchosia minima grown at Indian Institute of Pulses Research, Kanpur, India, showed yellow mosaic symptoms on leaves and were suspected to be caused by begomovirus(es). Leaves from five different plants (Rhm1-Rhm5) were tested for the presence of four viruses in PCR. PCR assays revealed the presence of mungbean yellow mosaic India virus in four samples, whereas one sample (Rhm2) was negative. Processing of Rhm2 sample using rolling circle amplification and restriction digestion indicated the presence of DNA molecules of ~ 2.6-2.7 kb. These molecules were sequenced after cloning and found to be of 2741 and 2658 nucleotides in size. BLAST analysis revealed that DNA-A (OQ269467) and DNA-B (OQ269468) molecules of rhynchosia yellow mosaic virus (RhYMV) with 99.09% and 93.74% nucleotide similarity with DNA-A (KP752090) and DNA-B (KP752091) of the RhYMV isolate, respectively. These sequences had a genome organization typical of legume-infecting Old World bipartite begomoviruses. Full genome sequences obtained from Rhm2 are, therefore, considered to be an isolate of RhYMV, designated as RhYMV-IN-Knp. The phylogenetic analysis revealed that RhYMV-IN-Knp was grouped with other isolates of RhYMV followed by Cajanus scarabaeoides yellow mosaic virus. DNA-A of RhYMV-IN-Knp showed two recombination events. The Old World bipartite begomovirus squash leaf curl China virus (AM260205) was identified as the major parent, whereas New World bipartite begomovirus rhynchosia golden yellow mosaic Yucatan virus (EU021216) was identified as the minor parent. RhYMV holds the potential of infecting cultivated legume crops, therefore regular monitoring is crucial especially for pigeonpea breeding programs.
生长在印度坎普尔印度豆类研究所的小喙花豆出现叶片黄花叶症状,怀疑是由双生病毒引起的。对五株不同植株(Rhm1 - Rhm5)的叶片进行PCR检测,以确定是否存在四种病毒。PCR检测显示,四个样本中存在绿豆黄花叶印度病毒,而一个样本(Rhm2)呈阴性。对Rhm2样本进行滚环扩增和限制性消化处理后,发现存在大小约为2.6 - 2.7 kb的DNA分子。这些分子经克隆后测序,发现大小分别为2741和2658个核苷酸。BLAST分析表明,喙豆花叶病毒(RhYMV)的DNA - A(OQ269467)和DNA - B(OQ269468)分子与RhYMV分离株的DNA - A(KP752090)和DNA - B(KP752091)的核苷酸相似性分别为99.09%和93.74%。这些序列具有感染豆科植物的旧世界二分体双生病毒典型的基因组结构。因此,从Rhm2获得的全基因组序列被认为是RhYMV的一个分离株,命名为RhYMV - IN - Knp。系统发育分析表明,RhYMV - IN - Knp与RhYMV的其他分离株聚在一起,其次是木豆叶甲黄花叶病毒。RhYMV - IN - Knp的DNA - A显示出两个重组事件。旧世界二分体双生病毒南瓜曲叶中国病毒(AM260205)被确定为主要亲本,而新世界二分体双生病毒喙豆花叶金黄花叶尤卡坦病毒(EU021216)被确定为次要亲本。RhYMV具有感染栽培豆科作物的潜力,因此定期监测至关重要,特别是对于木豆育种项目。