Fontenele Rafaela S, Lamas Natalia S, Lacorte Cristiano, Lacerda Ana Luiza M, Varsani Arvind, Ribeiro Simone G
Embrapa Recursos Genéticos e Biotecnologia, Brasília, Brazil; The Biodesign Center for Fundamental and Applied Microbiomics, Center for Evolution and Medicine, School of Life Sciences, Arizona State University, Tempe, AZ, 85287, USA.
Embrapa Recursos Genéticos e Biotecnologia, Brasília, Brazil.
Virus Res. 2017 Aug 15;240:175-179. doi: 10.1016/j.virusres.2017.08.007. Epub 2017 Aug 23.
Viruses in the family Geminiviridae have single-stranded DNA genomes encapsulated in geminate icosahedral particles. High throughput sequencing (HTS) for metagenomic approaches are being extensively used for the identification of known and novel viruses. Using a HTS approach, we identified a novel geminivirus in a tomato (Solanum lycopersicum) sample and a Cleome sp. sample collected in the midwest region of Brazil. The genomes from the two samples share 99.96% identity and ∼61-63% to genomes in the genus Capulavirus. The novel virus has been tentatively named tomato associated geminivirus 1 (TaGV1). No visual symptoms were observed in the field tomato plant or in the inoculated Nicotiana benthamiana where the virus established a systemic infection. The replication associated protein of TaGV1 is most similar to that encoded by capulaviruses (sharing 62-70% identity), whereas the CP is most similar to that of tomato pseudo curly top virus (sharing ∼31% identity). In the TaGV1 positive Cleome sp. sample, begomovirus DNA A and B components were also detected sharing 96% and 90% sequence identity to cleome leaf crumple virus DNA A and B components, respectively. Using a HTS approach, we identified TaGV1 in tomato and Cleome sp. samples and this is the first report of a geminivirus that is non-begomovirus in Brazil.
双生病毒科的病毒具有单链DNA基因组,包裹在双联体二十面体颗粒中。宏基因组学方法的高通量测序(HTS)正被广泛用于已知和新型病毒的鉴定。通过HTS方法,我们在巴西中西部地区采集的番茄(Solanum lycopersicum)样本和醉蝶花属样本中鉴定出一种新型双生病毒。这两个样本的基因组具有99.96%的同一性,与Capulavirus属的基因组具有约61-63%的同一性。这种新型病毒被暂时命名为番茄相关双生病毒1(TaGV1)。在田间番茄植株或接种的本氏烟草中未观察到可见症状,该病毒在接种的本氏烟草中建立了系统感染。TaGV1的复制相关蛋白与Capulavirus属病毒编码的蛋白最为相似(同一性为62-70%),而外壳蛋白与番茄伪卷叶顶病毒的最为相似(同一性约为31%)。在TaGV1阳性的醉蝶花属样本中,还检测到了菜豆金色花叶病毒属DNA A和B组分,它们与醉蝶花叶皱缩病毒DNA A和B组分的序列同一性分别为96%和90%。通过HTS方法,我们在番茄和醉蝶花属样本中鉴定出了TaGV1,这是巴西首次报道的非菜豆金色花叶病毒属双生病毒。