Cargando…

Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes

Numerous fungicide applications are required to control Erysiphe necator, the causative agent of powdery mildew. This increased demand for cultivars with strong and long-lasting field resistance to diseases and pests. In comparison to the susceptible cultivar ‘Teroldego’, the current study provides...

Descripción completa

Detalles Bibliográficos
Autores principales: Ciubotaru, Ramona Mihaela, Franceschi, Pietro, Vezzulli, Silvia, Zulini, Luca, Stefanini, Marco, Oberhuber, Michael, Robatscher, Peter, Chitarrini, Giulia, Vrhovsek, Urska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927228/
https://www.ncbi.nlm.nih.gov/pubmed/36798701
http://dx.doi.org/10.3389/fpls.2023.1112157
_version_ 1784888435461324800
author Ciubotaru, Ramona Mihaela
Franceschi, Pietro
Vezzulli, Silvia
Zulini, Luca
Stefanini, Marco
Oberhuber, Michael
Robatscher, Peter
Chitarrini, Giulia
Vrhovsek, Urska
author_facet Ciubotaru, Ramona Mihaela
Franceschi, Pietro
Vezzulli, Silvia
Zulini, Luca
Stefanini, Marco
Oberhuber, Michael
Robatscher, Peter
Chitarrini, Giulia
Vrhovsek, Urska
author_sort Ciubotaru, Ramona Mihaela
collection PubMed
description Numerous fungicide applications are required to control Erysiphe necator, the causative agent of powdery mildew. This increased demand for cultivars with strong and long-lasting field resistance to diseases and pests. In comparison to the susceptible cultivar ‘Teroldego’, the current study provides information on some promising disease-resistant varieties (mono-locus) carrying one E. necator-resistant locus: BC4 and ‘Kishmish vatkana’, as well as resistant genotypes carrying several E. necator resistant loci (pyramided): ‘Bianca’, F26P92, F13P71, and NY42. A clear picture of the metabolites’ alterations in response to the pathogen is shown by profiling the main and secondary metabolism: primary compounds and lipids; volatile organic compounds and phenolic compounds at 0, 12, and 48 hours after pathogen inoculation. We identified several compounds whose metabolic modulation indicated that resistant plants initiate defense upon pathogen inoculation, which, while similar to the susceptible genotype in some cases, did not imply that the plants were not resistant, but rather that their resistance was modulated at different percentages of metabolite accumulation and with different effect sizes. As a result, we discovered ten up-accumulated metabolites that distinguished resistant from susceptible varieties in response to powdery mildew inoculation, three of which have already been proposed as resistance biomarkers due to their role in activating the plant defense response.
format Online
Article
Text
id pubmed-9927228
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-99272282023-02-15 Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes Ciubotaru, Ramona Mihaela Franceschi, Pietro Vezzulli, Silvia Zulini, Luca Stefanini, Marco Oberhuber, Michael Robatscher, Peter Chitarrini, Giulia Vrhovsek, Urska Front Plant Sci Plant Science Numerous fungicide applications are required to control Erysiphe necator, the causative agent of powdery mildew. This increased demand for cultivars with strong and long-lasting field resistance to diseases and pests. In comparison to the susceptible cultivar ‘Teroldego’, the current study provides information on some promising disease-resistant varieties (mono-locus) carrying one E. necator-resistant locus: BC4 and ‘Kishmish vatkana’, as well as resistant genotypes carrying several E. necator resistant loci (pyramided): ‘Bianca’, F26P92, F13P71, and NY42. A clear picture of the metabolites’ alterations in response to the pathogen is shown by profiling the main and secondary metabolism: primary compounds and lipids; volatile organic compounds and phenolic compounds at 0, 12, and 48 hours after pathogen inoculation. We identified several compounds whose metabolic modulation indicated that resistant plants initiate defense upon pathogen inoculation, which, while similar to the susceptible genotype in some cases, did not imply that the plants were not resistant, but rather that their resistance was modulated at different percentages of metabolite accumulation and with different effect sizes. As a result, we discovered ten up-accumulated metabolites that distinguished resistant from susceptible varieties in response to powdery mildew inoculation, three of which have already been proposed as resistance biomarkers due to their role in activating the plant defense response. Frontiers Media S.A. 2023-01-31 /pmc/articles/PMC9927228/ /pubmed/36798701 http://dx.doi.org/10.3389/fpls.2023.1112157 Text en Copyright © 2023 Ciubotaru, Franceschi, Vezzulli, Zulini, Stefanini, Oberhuber, Robatscher, Chitarrini and Vrhovsek https://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
Ciubotaru, Ramona Mihaela
Franceschi, Pietro
Vezzulli, Silvia
Zulini, Luca
Stefanini, Marco
Oberhuber, Michael
Robatscher, Peter
Chitarrini, Giulia
Vrhovsek, Urska
Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes
title Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes
title_full Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes
title_fullStr Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes
title_full_unstemmed Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes
title_short Secondary and primary metabolites reveal putative resistance-associated biomarkers against Erysiphe necator in resistant grapevine genotypes
title_sort secondary and primary metabolites reveal putative resistance-associated biomarkers against erysiphe necator in resistant grapevine genotypes
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927228/
https://www.ncbi.nlm.nih.gov/pubmed/36798701
http://dx.doi.org/10.3389/fpls.2023.1112157
work_keys_str_mv AT ciubotaruramonamihaela secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT franceschipietro secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT vezzullisilvia secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT zuliniluca secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT stefaninimarco secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT oberhubermichael secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT robatscherpeter secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT chitarrinigiulia secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes
AT vrhovsekurska secondaryandprimarymetabolitesrevealputativeresistanceassociatedbiomarkersagainsterysiphenecatorinresistantgrapevinegenotypes