Raj S K, Kumar S, Snehi S K, Pathre U
Molecular Virology, National Botanical Research Institute (NBRI).
Plant Physiology, NBRI, Lucknow-226 001, India.
Plant Dis. 2008 Jan;92(1):171. doi: 10.1094/PDIS-92-1-0171C.
Jatropha curcas L. is a major commercial biodiesel fuel crop grown on 98 million acres (39.66 million ha) in India. Severe mosaic disease accompanied by yellow spots was noticed on 15% of J. curcas growing in the experimental plots of NBRI, Lucknow, India, during October of 2006. Inoculations with sap from symptomatic plants resulted in systemic mosaic on three of seven J. curcas seedlings. Gel diffusion tests were performed with antiserum to Cucumber mosaic virus (CMV), Tobacco ringspot virus, and Chrysanthemum virus B (PVAS-242a, PVAS-157, and PVAS-349, respectively; ATCC, Manassas, VA). Leaf sap of infected plants reacted only with PVAS-242a, indicating the presence of CMV. Reverse transcription (RT)-PCR assays with CMV coat protein gene specific primers (Genbank Accession Nos. AM180922 and AM180923) and total nucleic acid extracted from symptomatic J. curcas leaf tissue yielded the expected ~650-bp amplicon, which was cloned and sequenced (GenBank Accession No. EF153739). BLAST analysis indicated 98 to 99% nucleotide identity with CMV isolates (GenBank Accession Nos. DQ914877, DQ640743, AF350450, AF281864, X89652, AF198622, DQ152254, DQ141675, and DQ028777). Phylogenetic analysis showed that the J. curcas isolate was more closely related to Indian isolates of CMV belonging to subgroup Ib. Literature surveys revealed records of Jatropha mosaic virus on J. gossypiifolia in Puerto Rico (1) and on J. curcas in India (2). To our knowledge, this is the first report of CMV on J. curcas. References: (1) J. K. Brown et al. Arch. Virol. 146:1581, 2001. (2) D. S. A. Narayana et al. Curr. Sci. 91:584, 2006.
麻疯树是印度种植面积达9800万英亩(3966万公顷)的一种主要商业生物柴油燃料作物。2006年10月,在印度勒克瑙国家植物研究所的试验田中,15%的麻疯树出现了严重的花叶病并伴有黄斑。用有症状植株的汁液接种七株麻疯树幼苗中的三株后,出现了系统花叶症状。用抗黄瓜花叶病毒(CMV)、烟草环斑病毒和菊花B病毒(分别为PVAS - 242a、PVAS - 157和PVAS - 349;美国典型培养物保藏中心,弗吉尼亚州马纳萨斯)的抗血清进行了凝胶扩散试验。受感染植株的叶汁仅与PVAS - 242a发生反应,表明存在CMV。用CMV外壳蛋白基因特异性引物(Genbank登录号:AM180922和AM180923)以及从有症状的麻疯树叶片组织中提取的总核酸进行逆转录(RT)-PCR分析,得到了预期的约650碱基对的扩增产物,将其克隆并测序(GenBank登录号:EF153739)。BLAST分析表明,其与CMV分离株(GenBank登录号:DQ914877、DQ640743、AF350450、AF281864、X89652、AF198622、DQ152254、DQ141675和DQ028777)的核苷酸同一性为98%至99%。系统发育分析表明,麻疯树分离株与属于Ib亚组的印度CMV分离株关系更密切。文献调查显示,波多黎各的棉叶麻疯树上有麻疯树花叶病毒记录(1),印度的麻疯树上也有该病毒记录(2)。据我们所知,这是关于CMV在麻疯树上的首次报道。参考文献:(1)J.K.布朗等人,《病毒学档案》146:1581,2001年。(2)D.S.A.纳拉亚纳等人,《当代科学》91:584,2006年。