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Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera

Plasmopara viticola (Berk. et Curt.) Berl. and de Toni, the agent of downy mildew, is one of the most important pathogens of European grapevine (Vitis vinifera L.). Extensive evaluation of cultivated grapevine germplasm has highlighted the existence of resistant phenotypes in the Georgian (Southern...

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Autores principales: Sargolzaei, Maryam, Maddalena, Giuliana, Bitsadze, Nana, Maghradze, David, Bianco, Piero Attilio, Failla, Osvaldo, Toffolatti, Silvia Laura, De Lorenzis, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583455/
https://www.ncbi.nlm.nih.gov/pubmed/33163011
http://dx.doi.org/10.3389/fpls.2020.562432
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author Sargolzaei, Maryam
Maddalena, Giuliana
Bitsadze, Nana
Maghradze, David
Bianco, Piero Attilio
Failla, Osvaldo
Toffolatti, Silvia Laura
De Lorenzis, Gabriella
author_facet Sargolzaei, Maryam
Maddalena, Giuliana
Bitsadze, Nana
Maghradze, David
Bianco, Piero Attilio
Failla, Osvaldo
Toffolatti, Silvia Laura
De Lorenzis, Gabriella
author_sort Sargolzaei, Maryam
collection PubMed
description Plasmopara viticola (Berk. et Curt.) Berl. and de Toni, the agent of downy mildew, is one of the most important pathogens of European grapevine (Vitis vinifera L.). Extensive evaluation of cultivated grapevine germplasm has highlighted the existence of resistant phenotypes in the Georgian (Southern Caucasus) germplasm. Resistance is shown as a reduction in disease severity. Unraveling the genetic architecture of grapevine response to P. viticola infection is crucial to develop resistant varieties and reduce the impact of disease management. The aim of this work was to apply a genome-wide association (GWA) approach to a panel of Georgian-derived accessions phenotyped for P. viticola susceptibility and genotyped with Vitis18kSNP chip array. GWA identified three highly significant novel loci on chromosomes 14 (Rpv29), 3 (Rpv30) and 16 (Rpv31) associated with a low level of pathogen sporulation. Rpv29, Rpv30, and Rpv31 loci appeared to be associated with plant defense genes against biotic stresses, such as genes involved in pathogen recognition and signal transduction. This study provides the first evidence of resistant loci against P. viticola in V. vinifera germplasm, and identifies potential target genes for breeding P. viticola resistant grapevine cultivars.
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spelling pubmed-75834552020-11-05 Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera Sargolzaei, Maryam Maddalena, Giuliana Bitsadze, Nana Maghradze, David Bianco, Piero Attilio Failla, Osvaldo Toffolatti, Silvia Laura De Lorenzis, Gabriella Front Plant Sci Plant Science Plasmopara viticola (Berk. et Curt.) Berl. and de Toni, the agent of downy mildew, is one of the most important pathogens of European grapevine (Vitis vinifera L.). Extensive evaluation of cultivated grapevine germplasm has highlighted the existence of resistant phenotypes in the Georgian (Southern Caucasus) germplasm. Resistance is shown as a reduction in disease severity. Unraveling the genetic architecture of grapevine response to P. viticola infection is crucial to develop resistant varieties and reduce the impact of disease management. The aim of this work was to apply a genome-wide association (GWA) approach to a panel of Georgian-derived accessions phenotyped for P. viticola susceptibility and genotyped with Vitis18kSNP chip array. GWA identified three highly significant novel loci on chromosomes 14 (Rpv29), 3 (Rpv30) and 16 (Rpv31) associated with a low level of pathogen sporulation. Rpv29, Rpv30, and Rpv31 loci appeared to be associated with plant defense genes against biotic stresses, such as genes involved in pathogen recognition and signal transduction. This study provides the first evidence of resistant loci against P. viticola in V. vinifera germplasm, and identifies potential target genes for breeding P. viticola resistant grapevine cultivars. Frontiers Media S.A. 2020-10-08 /pmc/articles/PMC7583455/ /pubmed/33163011 http://dx.doi.org/10.3389/fpls.2020.562432 Text en Copyright © 2020 Sargolzaei, Maddalena, Bitsadze, Maghradze, Bianco, Failla, Toffolatti and De Lorenzis. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Sargolzaei, Maryam
Maddalena, Giuliana
Bitsadze, Nana
Maghradze, David
Bianco, Piero Attilio
Failla, Osvaldo
Toffolatti, Silvia Laura
De Lorenzis, Gabriella
Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera
title Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera
title_full Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera
title_fullStr Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera
title_full_unstemmed Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera
title_short Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera
title_sort rpv29, rpv30 and rpv31: three novel genomic loci associated with resistance to plasmopara viticola in vitis vinifera
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583455/
https://www.ncbi.nlm.nih.gov/pubmed/33163011
http://dx.doi.org/10.3389/fpls.2020.562432
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