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Erschienen in: Archives of Virology 10/2014

01.10.2014 | Brief Report

Phylogenetic and recombination analysis of the homing protein domain of grapevine fanleaf virus (GFLV) isolates associated with ‘yellow mosaic’ and ‘infectious malformation’ syndromes in grapevine

verfasst von: Toufic Elbeaino, Hulusi Kiyi, Reza Boutarfa, Angelantonio Minafra, Giovanni Paolo Martelli, Michele Digiaro

Erschienen in: Archives of Virology | Ausgabe 10/2014

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Abstract

The RNA2 of seven grapevine fanleaf virus (GFLV) isolates from vines with yellow mosaic (YM) symptoms from different origin were sequenced. These sequences showed a high variability in the homing protein (2AHP) and, in five of them, a putative recombination with arabis mosaic virus (ArMV) was detected. To investigate recombination frequency, the partial sequences of the 2AHP of 28 additional GFLV isolates from nine different countries, showing either YM or infectious malformations (MF) symptoms, were obtained and compared with those of GFLV isolates from GenBank. The analysis confirmed the high level of sequence variability (up to 41 % at the nucleotide level) among isolates. In phylogenetic trees constructed using different approaches, the sequenced isolates always clustered in four conserved groups, three of which comprised YM strains (groups 1, 2 and 3), and one (group 4) the MF strains. Potential interspecific recombination sites between GFLV and ArMV were predicted in the 2AHP gene of several isolates, all of which were associated with YM symptoms.
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Metadaten
Titel
Phylogenetic and recombination analysis of the homing protein domain of grapevine fanleaf virus (GFLV) isolates associated with ‘yellow mosaic’ and ‘infectious malformation’ syndromes in grapevine
verfasst von
Toufic Elbeaino
Hulusi Kiyi
Reza Boutarfa
Angelantonio Minafra
Giovanni Paolo Martelli
Michele Digiaro
Publikationsdatum
01.10.2014
Verlag
Springer Vienna
Erschienen in
Archives of Virology / Ausgabe 10/2014
Print ISSN: 0304-8608
Elektronische ISSN: 1432-8798
DOI
https://doi.org/10.1007/s00705-014-2138-8

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