Variability of the 3' terminal of the polymerase gene of Grapevine leafroll-associated virus 3 isolates from Vale do São Francisco, Brazil.

• Autor(a) principal: DIANESE, E. de C.
• Data de Publicação: 2005
• Outros Autores: RAMALHO, E. D., CERQUEIRA, D. M., LOPES, D. B., FAJARDO, T. V. M., FERREIRA, M. A. S. V., MARTINS, C. R. F.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
• Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/155711
• topic: Videira; Polimerase; GLRa-3; Vitis spp; Brasil; Vale do São francisco; Doença; RNA; Uva; Vírus; Ampelovirus

Many viral diseases, including leafroll, which is of great economic importance, affect grapevines (Vitis spp.). Acomplex of eight viruses [Grapevine leafroll-associated virus (GLRaV)-1 to 8] is associated with this disease. The objectiveof this study was to compare the variability of the 3? terminal region of the polymerase gene of three isolates of GLRaV-3 (Grapevine leafroll-associated virus-3), from Submédio do Vale do Rio São Francisco (Petrolina-PE) with that of other isolates available at the GenBank, including an isolate from North America and another from Southern Brazil. The viral RNA was extracted from three infected ELISA reactive plants and a fragment of 340 bp was amplified, by RT-PCR, using primers that recognize that portion of the polymerase gene found between nucleotides 8267 and 8606. The three isolates from Vale do Rio São Francisco named Pet-1, Pet-2 and Pet-3, showed similarities ranging from 98% and 94%, respectively to the isolates from North America (AF037268) and Southern Brazilian (AF438411). Considering the whole genome, the main variation found was one amino acid change at position 2766 (F2766Y). These preliminary data indicate the existence of a natural variation among GLRaV-3 isolates from grapevines. This could be due to the vegetative propagation and long cycle of the plant, associated with the error-prone nature of RNA-dependent RNA polymerase.