Kushawaha A K, Rabindran R, Dasgupta I
Acta Virol. 2015 Mar;59(1):57-63. doi: 10.4149/av_2015_01_63.
The complete nucleotide sequence of Sri Lankan cassava mosaic virus (SLCMV) DNA-A isolated from cassava in southern India was analyzed, a phylogenetic analysis with other begomoviral nucleotide sequences was performed and an efficient inoculation method of Nicotiana benthamiana with the cloned DNA was developed utilizing a biolistic device. The nucleotide sequence showed the conservation of all functional begomoviral protein domains and aligned most closely with begomoviruses reported from the Indian subcontinent, except for begomoviruses of cucurbits and legumes. Upon biolistic inoculation of N. benthamiana with the cloned DNA, most plants became symptomatic and showed the accumulation of viral DNA within 21-28 days post-inoculation.
对从印度南部木薯中分离出的斯里兰卡木薯花叶病毒(SLCMV)DNA-A的完整核苷酸序列进行了分析,与其他双生病毒核苷酸序列进行了系统发育分析,并利用生物弹道装置开发了一种用克隆DNA高效接种本氏烟草的方法。核苷酸序列显示出所有功能性双生病毒蛋白结构域的保守性,并且与印度次大陆报道的双生病毒最为接近,除了葫芦科和豆科的双生病毒。用克隆DNA对本氏烟草进行生物弹道接种后,大多数植株出现症状,并在接种后21-28天内显示出病毒DNA的积累。