Rathore S, Bhatt B S, Yadav B K, Kale R K, Singh A K
School of Life Sciences, Central University of Gujarat, Gandhinagar-382030 Gujarat, India.
Plant Dis. 2014 Mar;98(3):428. doi: 10.1094/PDIS-07-13-0719-PDN.
In December 2012, tomato leaf curl disease (ToLCD) (2) was observed in tomato-growing areas of Gandhinagar District of Gujarat, a state in northwestern India. Incidence of ToLCD was estimated to be between 40 and 70% depending on the cultivars used. Infected plants exhibited symptoms consisting of leaf rolling, leaf curling, and yellowing typical of begomoviruses. Total DNA was isolated from a single affected tomato plant (2). Begomovirus infection in this sample was established by amplification of the expected-size 550-bp DNA fragment from this extract by PCR with degenerate DNA-A primers (3). Rolling circle amplification (RCA) using ϕ29 DNA polymerase was carried out on the total DNA, followed by digestion with Bam HI. An amplicon of ~2.8 kb was gel-eluted and cloned into Bam HI linearized pBluescript II KS(+). Restriction enzyme digestion of plasmid DNA from the resulting clones indicated the presence of one type of molecule. Using PCR and universal betasatellite primers, the expected 1.3-kb fragment was amplified from the DNA extract (1). An amplicon of ~1.3 kb was gel-eluted and cloned into pTZ57RT vector. Sequence analysis revealed that DNA-A (GenBank Accession No. KC952005) is composed of 2,753 nt and showed the highest identity (87.8%) with Tomato leaf curl Kerala virus[India:Kerala:2008] (GenBank Accession No. EU910141). An analysis for recombination showed this begomovirus DNA likely to have originated by recombination between Tomato leaf curl Kerala virus and Tomato leaf curl Karnataka virus. The satellite DNA-β (GenBank Accession No. KC952006) is composed of 1,365 nt and showed the highest identity (75.6%) with Tomato leaf curl betasatellite[India:Ludhiana:2004] (ToLCB-[IN:Lud:04]) (GenBank Accession No. AY765255). On the basis of DNA-A sequence analysis, the ICTV species demarcation criteria of 89% DNA-A sequence identity, and genome organization, the present isolate was considered as a new begomovirus species and named Tomato leaf curl Gandhinagar virus (ToLCGNV). The betasatellite shares less than 78% identity with (ToLCB-[IN:Lud:04]), it is considered a new species of betasatellite and the name, Tomato leaf curl Gandhinagar betasatellite (ToLCGNB) is proposed. Multimeric clones of the begomovirus and betasatellite DNAs were generated in a binary vector and these plasmids transformed into Agrobacterium tumefaciens. Nicotiana benthamiana and tomato plants agroinoculated with the cloned begomovirus DNA developed leaf curl symptoms, whereas plants co-agroinoculated with the cloned begomovirus and betasatellites developed more severe symptoms, including leaf rolling, leaf curling, and yellowing. The symptoms induced by the begomovirus and betasatellite DNAs were indistinguishable from those observed in the field. Thus, ToLCGNV is a new monopartite begomovirus which, in association with a new species of betasatellite, causes ToLCD in Gandhinagar, India. The presence of ToLCGNV needs to be considered, along with the already reported begomoviruses infecting tomatoes in this state, e.g., Tomato leaf curl Gujarat virus (2), in studies aimed to developing tomato cultivars with stable resistance to these tomato-infecting begomoviruses in India. References: (1) R. W. Briddon et al. Mol. Biotechnol. 20:315, 2002. (2) C. Reddy et al. Arch Virol. 150:845, 2005. (3) S. D. Wyatt and J. K. Brown. Phytopathology 86:1288, 1996.
2012年12月,在印度西北部古吉拉特邦甘地讷格尔区的番茄种植区发现了番茄卷叶病(ToLCD)(2)。根据所种植的品种不同,ToLCD的发病率估计在40%至70%之间。受感染的植株表现出典型的双生病毒症状,包括叶片上卷、卷曲和黄化。从一株受影响的番茄植株中提取了总DNA(2)。通过使用简并DNA-A引物进行PCR,从该提取物中扩增出预期大小为550 bp的DNA片段,从而确定该样本中存在双生病毒感染(3)。使用ϕ29 DNA聚合酶对总DNA进行滚环扩增(RCA),随后用Bam HI进行酶切。将约2.8 kb的扩增子进行凝胶洗脱,并克隆到用Bam HI线性化的pBluescript II KS(+)载体中。对所得克隆的质粒DNA进行限制性酶切分析表明存在一种类型的分子。使用PCR和通用卫星DNA引物,从DNA提取物中扩增出预期的1.3 kb片段(1)。将约1.3 kb的扩增子进行凝胶洗脱,并克隆到pTZ57RT载体中。序列分析表明,DNA-A(GenBank登录号KC952005)由2753个核苷酸组成,与番茄卷叶喀拉拉邦病毒[印度:喀拉拉邦:2008](GenBank登录号EU910141)具有最高的同一性(87.8%)。重组分析表明,这种双生病毒DNA可能起源于番茄卷叶喀拉拉邦病毒和番茄卷叶卡纳塔克邦病毒之间的重组。卫星DNA-β(GenBank登录号KC952006)由1365个核苷酸组成,与番茄卷叶卫星DNA[印度:卢迪亚纳:2004](ToLCB-[IN:Lud:04])(GenBank登录号AY765255)具有最高的同一性(75.6%)。根据DNA-A序列分析、ICTV物种划分标准(DNA-A序列同一性为89%)和基因组结构,该分离株被认为是一种新的双生病毒物种,并命名为番茄卷叶甘地讷格尔病毒(ToLCGNV)。该卫星DNA与(ToLCB-[IN:Lud:04])的同一性低于78%,因此被认为是一种新的卫星DNA物种,并被命名为番茄卷叶甘地讷格尔卫星DNA(ToLCGNB)。在二元载体中构建了双生病毒和卫星DNA的多聚体克隆,并将这些质粒转化到根癌农杆菌中。用克隆的双生病毒DNA进行农杆菌接种的本氏烟草和番茄植株出现了卷叶症状,而用克隆的双生病毒和卫星DNA共同进行农杆菌接种的植株出现了更严重的症状,包括叶片上卷、卷曲和黄化。双生病毒和卫星DNA诱导的症状与在田间观察到的症状无法区分。因此,ToLCGNV是一种新的单分体双生病毒,与一种新的卫星DNA物种相关联,在印度甘地讷格尔导致ToLCD。在旨在培育对印度这些感染番茄的双生病毒具有稳定抗性的番茄品种的研究中,需要考虑ToLCGNV的存在,以及该邦已经报道的感染番茄的双生病毒,例如番茄卷叶古吉拉特病毒(2)。参考文献:(1)R. W. Briddon等人,《分子生物技术》20:315,2002年。(2)C. Reddy等人,《病毒学档案》150:845,2005年。(3)S. D. Wyatt和J. K. Brown,《植物病理学》86:1288,1996年。