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Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design
Grapevine leafroll-associated virus 3 (GLRaV-3) is the most widely prevalent and economically important of the complex of RNA viruses associated with grapevine leafroll disease (GLD). Phylogenetic studies have grouped GLRaV-3 isolates into nine different monophyletic groups and four supergroups, mak...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291115/ https://www.ncbi.nlm.nih.gov/pubmed/30540844 http://dx.doi.org/10.1371/journal.pone.0208862 |
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author | Diaz-Lara, Alfredo Klaassen, Vicki Stevens, Kristian Sudarshana, Mysore R. Rowhani, Adib Maree, Hans J. Chooi, Kar Mun Blouin, Arnaud G. Habili, Nuredin Song, Yashu Aram, Kamyar Arnold, Kari Cooper, Monica L. Wunderlich, Lynn Battany, Mark C. Bettiga, Larry J. Smith, Rhonda J. Bester, Rachelle Xiao, Huogen Meng, Baozhong Preece, John E. Golino, Deborah Al Rwahnih, Maher |
author_facet | Diaz-Lara, Alfredo Klaassen, Vicki Stevens, Kristian Sudarshana, Mysore R. Rowhani, Adib Maree, Hans J. Chooi, Kar Mun Blouin, Arnaud G. Habili, Nuredin Song, Yashu Aram, Kamyar Arnold, Kari Cooper, Monica L. Wunderlich, Lynn Battany, Mark C. Bettiga, Larry J. Smith, Rhonda J. Bester, Rachelle Xiao, Huogen Meng, Baozhong Preece, John E. Golino, Deborah Al Rwahnih, Maher |
author_sort | Diaz-Lara, Alfredo |
collection | PubMed |
description | Grapevine leafroll-associated virus 3 (GLRaV-3) is the most widely prevalent and economically important of the complex of RNA viruses associated with grapevine leafroll disease (GLD). Phylogenetic studies have grouped GLRaV-3 isolates into nine different monophyletic groups and four supergroups, making GLRaV-3 a genetically highly diverse virus species. In addition, new divergent variants have been discovered recently around the world. Accurate identification of the virus is an essential component in the management and control of GLRaV-3; however, the diversity of GLRaV-3, coupled with the limited sequence information, have complicated the development of a reliable detection assay. In this study, GLRaV-3 sequence data available in GenBank and those generated at Foundation Plant Services, University of California-Davis, was used to develop a new RT-qPCR assay with the capacity to detect all known GLRaV-3 variants. The new assay, referred to as FPST, was challenged against samples that included plants infected with different GLRaV-3 variants and originating from 46 countries. The FPST assay detected all known GLRaV-3 variants, including the highly divergent variants, by amplifying a small highly conserved region in the 3’ untranslated terminal region (UTR) of the virus genome. The reliability of the new RT-qPCR assay was confirmed by an enzyme linked immunosorbent assay (ELISA) that can detect all known GLRaV-3 variants characterized to date. Additionally, three new GLRaV-3 divergent variants, represented by four isolates, were identified using a hierarchical testing process involving the FPST assay, GLRaV-3 variant-specific assays and high-throughput sequencing analysis. These variants were distantly related to groups I, II, III, V, VI, VII and IX, but much similar to GLRaV-3 variants with no assigned group; thus, they may represent new clades. Finally, based on the phylogenetic analysis, a new GLRaV-3 subclade is proposed and named as group X. |
format | Online Article Text |
id | pubmed-6291115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62911152018-12-28 Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design Diaz-Lara, Alfredo Klaassen, Vicki Stevens, Kristian Sudarshana, Mysore R. Rowhani, Adib Maree, Hans J. Chooi, Kar Mun Blouin, Arnaud G. Habili, Nuredin Song, Yashu Aram, Kamyar Arnold, Kari Cooper, Monica L. Wunderlich, Lynn Battany, Mark C. Bettiga, Larry J. Smith, Rhonda J. Bester, Rachelle Xiao, Huogen Meng, Baozhong Preece, John E. Golino, Deborah Al Rwahnih, Maher PLoS One Research Article Grapevine leafroll-associated virus 3 (GLRaV-3) is the most widely prevalent and economically important of the complex of RNA viruses associated with grapevine leafroll disease (GLD). Phylogenetic studies have grouped GLRaV-3 isolates into nine different monophyletic groups and four supergroups, making GLRaV-3 a genetically highly diverse virus species. In addition, new divergent variants have been discovered recently around the world. Accurate identification of the virus is an essential component in the management and control of GLRaV-3; however, the diversity of GLRaV-3, coupled with the limited sequence information, have complicated the development of a reliable detection assay. In this study, GLRaV-3 sequence data available in GenBank and those generated at Foundation Plant Services, University of California-Davis, was used to develop a new RT-qPCR assay with the capacity to detect all known GLRaV-3 variants. The new assay, referred to as FPST, was challenged against samples that included plants infected with different GLRaV-3 variants and originating from 46 countries. The FPST assay detected all known GLRaV-3 variants, including the highly divergent variants, by amplifying a small highly conserved region in the 3’ untranslated terminal region (UTR) of the virus genome. The reliability of the new RT-qPCR assay was confirmed by an enzyme linked immunosorbent assay (ELISA) that can detect all known GLRaV-3 variants characterized to date. Additionally, three new GLRaV-3 divergent variants, represented by four isolates, were identified using a hierarchical testing process involving the FPST assay, GLRaV-3 variant-specific assays and high-throughput sequencing analysis. These variants were distantly related to groups I, II, III, V, VI, VII and IX, but much similar to GLRaV-3 variants with no assigned group; thus, they may represent new clades. Finally, based on the phylogenetic analysis, a new GLRaV-3 subclade is proposed and named as group X. Public Library of Science 2018-12-12 /pmc/articles/PMC6291115/ /pubmed/30540844 http://dx.doi.org/10.1371/journal.pone.0208862 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Diaz-Lara, Alfredo Klaassen, Vicki Stevens, Kristian Sudarshana, Mysore R. Rowhani, Adib Maree, Hans J. Chooi, Kar Mun Blouin, Arnaud G. Habili, Nuredin Song, Yashu Aram, Kamyar Arnold, Kari Cooper, Monica L. Wunderlich, Lynn Battany, Mark C. Bettiga, Larry J. Smith, Rhonda J. Bester, Rachelle Xiao, Huogen Meng, Baozhong Preece, John E. Golino, Deborah Al Rwahnih, Maher Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design |
title | Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design |
title_full | Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design |
title_fullStr | Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design |
title_full_unstemmed | Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design |
title_short | Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design |
title_sort | characterization of grapevine leafroll-associated virus 3 genetic variants and application towards rt-qpcr assay design |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291115/ https://www.ncbi.nlm.nih.gov/pubmed/30540844 http://dx.doi.org/10.1371/journal.pone.0208862 |
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