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first description of grapevine leafroll-associated virus 5 in argentina and partial genome sequence.an accession of vitis vinifera cv. red globe from argentina, was found to be infected with grapevine leafroll-associated virus-5 by elisa. it was partially sequenced, and three orfs, corresponding to hsp70h, hsp90h, and cp, were found. this isolate shares a high aminoacid identity with the previously reported sequence of the virus, and identities between 80% and 90% with previously reported glrav-9 and glrav-4 isolates. the analysis of the sequence supports the clustering together with glrav-4 a ...200918953643
occurrence of grapevine leafroll-associated virus 5 in portugal: genetic variability and population structure in field-grown grapevines.a comparison of 15 field isolates of grapevine leafroll-associated virus 5 (glrav-5) was conducted, based on the analysis of nucleotide sequences of two viral orfs: the coat protein (cp) and the heat shock protein 90 homolog (hsp90h). after amplification and cloning, the population of viral sequences was analyzed for each isolate, revealing the within-isolate presence of sequence variants for both genes, with one or more major cp variants. phylogenetic analysis showed the gene sequence variants ...201222692680
genomic analysis of grapevine leafroll associated virus-5 and related viruses.the grapevine leafroll-associated viruses (glravs) (closteroviridae) represent an emerging threat to world grape production. one group of glravs within the genus ampelovirus, the glrav-4-like viruses (glrav-4lvs), contains a fragmented collection of seven viruses only two of which (glrav-pr and glracv) are fully sequenced. here in reporting the sequence of glrav-5, a member of glrav-4lvs, we identify genomic elements common to the glrav-4lv group. exclusive properties include a highly conserved ...201121893115
a strategy for rapid cdna cloning from double-stranded rna templates isolated from plants infected with rna viruses by using taq dna polymerase.a fast and efficient cdna cloning procedure for plant rna viruses was developed. in this procedure, double-stranded rna (dsrna) was used as a template source. standard cdna synthesis reagents and random hexamers were then used for making cdnas. taq dna polymerase was used to add additional (a) at the ends of cdnas, a ta cloning kit to ligate the cdnas to vectors, and an electroporator to transform the dnas to e. coli cells. dsrnas were extracted from grapevine tissues infected with four differen ...200010644087
partial genome organization, identification of the coat protein gene, and detection of grapevine leafroll-associated virus-5.abstract the genome of grapevine leafroll-associated virus-5 (glrav-5) was cloned, and the sequence of 4766 nt was determined. degenerate oligonucleotide primers designed from the conserved closterovirus heat shock 70 protein (hsp 70) homologue were used to obtain viral-specific sequences to anchor the cloning of the viral rna with a genomic walking approach. the partial nucleotide (nt) sequence of glrav-5 showed the presence of four open reading frames (orf a through d), potentially coding for ...200118943347
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