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Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine

Grapevine line pattern virus (GLPV) was first described 30 years ago in Hungary. The lack of its genomic sequences and of an available antiserum made its detection impossible in other parts of the world. Three different high-throughput sequencing (HTS) protocols applied on a GLPV-infected vine allow...

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Autores principales: Elbeaino, Toufic, Kontra, Levente, Demian, Emese, Jaksa-Czotter, Nikoletta, Slimen, Amani Ben, Fabian, Richard, Lazar, Janos, Tamisier, Lucie, Digiaro, Michele, Massart, Sebastien, Varallyay, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354484/
https://www.ncbi.nlm.nih.gov/pubmed/32486454
http://dx.doi.org/10.3390/v12060602
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author Elbeaino, Toufic
Kontra, Levente
Demian, Emese
Jaksa-Czotter, Nikoletta
Slimen, Amani Ben
Fabian, Richard
Lazar, Janos
Tamisier, Lucie
Digiaro, Michele
Massart, Sebastien
Varallyay, Eva
author_facet Elbeaino, Toufic
Kontra, Levente
Demian, Emese
Jaksa-Czotter, Nikoletta
Slimen, Amani Ben
Fabian, Richard
Lazar, Janos
Tamisier, Lucie
Digiaro, Michele
Massart, Sebastien
Varallyay, Eva
author_sort Elbeaino, Toufic
collection PubMed
description Grapevine line pattern virus (GLPV) was first described 30 years ago in Hungary. The lack of its genomic sequences and of an available antiserum made its detection impossible in other parts of the world. Three different high-throughput sequencing (HTS) protocols applied on a GLPV-infected vine allowed the construction of the full genome sequence of this virus. It includes three RNA segments, encoding four proteins: methyltransferase-helicase (1a), RNA-dependent RNA polymerase (2a), movement protein (3a) and coat protein (3b). The obtained sequences were used to design specific primers for its detection by RT-PCR and Northern blot hybridization, respectively. These diagnostic methods were used to test the presence of GLPV in graft-inoculated plants and in 220 grapevine accessions of different Mediterranean origins. The three RNAs-encoding proteins of GLPV shared a very high amino acid identity with those of hop yellow virus, a tentative member of the Anulavirus genus, leaving no doubt that both are two isolates of the same viral species. A circular RNA originating from the RNA2 was found, for which an alternative silencing suppressor role is hypothesized. Further investigation is needed to determine this possibility and also the host range and pathological significance of the virus.
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spelling pubmed-73544842020-08-05 Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine Elbeaino, Toufic Kontra, Levente Demian, Emese Jaksa-Czotter, Nikoletta Slimen, Amani Ben Fabian, Richard Lazar, Janos Tamisier, Lucie Digiaro, Michele Massart, Sebastien Varallyay, Eva Viruses Article Grapevine line pattern virus (GLPV) was first described 30 years ago in Hungary. The lack of its genomic sequences and of an available antiserum made its detection impossible in other parts of the world. Three different high-throughput sequencing (HTS) protocols applied on a GLPV-infected vine allowed the construction of the full genome sequence of this virus. It includes three RNA segments, encoding four proteins: methyltransferase-helicase (1a), RNA-dependent RNA polymerase (2a), movement protein (3a) and coat protein (3b). The obtained sequences were used to design specific primers for its detection by RT-PCR and Northern blot hybridization, respectively. These diagnostic methods were used to test the presence of GLPV in graft-inoculated plants and in 220 grapevine accessions of different Mediterranean origins. The three RNAs-encoding proteins of GLPV shared a very high amino acid identity with those of hop yellow virus, a tentative member of the Anulavirus genus, leaving no doubt that both are two isolates of the same viral species. A circular RNA originating from the RNA2 was found, for which an alternative silencing suppressor role is hypothesized. Further investigation is needed to determine this possibility and also the host range and pathological significance of the virus. MDPI 2020-05-31 /pmc/articles/PMC7354484/ /pubmed/32486454 http://dx.doi.org/10.3390/v12060602 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Elbeaino, Toufic
Kontra, Levente
Demian, Emese
Jaksa-Czotter, Nikoletta
Slimen, Amani Ben
Fabian, Richard
Lazar, Janos
Tamisier, Lucie
Digiaro, Michele
Massart, Sebastien
Varallyay, Eva
Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine
title Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine
title_full Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine
title_fullStr Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine
title_full_unstemmed Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine
title_short Complete Sequence, Genome Organization and Molecular Detection of Grapevine Line Pattern Virus, a New Putative Anulavirus Infecting Grapevine
title_sort complete sequence, genome organization and molecular detection of grapevine line pattern virus, a new putative anulavirus infecting grapevine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354484/
https://www.ncbi.nlm.nih.gov/pubmed/32486454
http://dx.doi.org/10.3390/v12060602
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