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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7354484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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