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The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola

Downy mildew, caused by Plasmopara viticola, is one of the most severe diseases of grapevine (Vitis vinifera L.). Genetic resistance is an effective and sustainable control strategy, but major resistance genes (encoding receptors for specific pathogen effectors) introgressed from wild Vitis species,...

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Autores principales: Vandelle, Elodie, Ariani, Pietro, Regaiolo, Alice, Danzi, Davide, Lovato, Arianna, Zadra, Claudia, Vitulo, Nicola, Gambino, Giorgio, Polverari, Annalisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833427/
https://www.ncbi.nlm.nih.gov/pubmed/33477914
http://dx.doi.org/10.3390/ijms22020940
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author Vandelle, Elodie
Ariani, Pietro
Regaiolo, Alice
Danzi, Davide
Lovato, Arianna
Zadra, Claudia
Vitulo, Nicola
Gambino, Giorgio
Polverari, Annalisa
author_facet Vandelle, Elodie
Ariani, Pietro
Regaiolo, Alice
Danzi, Davide
Lovato, Arianna
Zadra, Claudia
Vitulo, Nicola
Gambino, Giorgio
Polverari, Annalisa
author_sort Vandelle, Elodie
collection PubMed
description Downy mildew, caused by Plasmopara viticola, is one of the most severe diseases of grapevine (Vitis vinifera L.). Genetic resistance is an effective and sustainable control strategy, but major resistance genes (encoding receptors for specific pathogen effectors) introgressed from wild Vitis species, although effective, may be non-durable because the pathogen can evolve to avoid specific recognition. Previous transcriptomic studies in the resistant species Vitis riparia highlighted the activation of signal transduction components during infection. The transfer of such components to V. vinifera might confer less specific and therefore more durable resistance. Here, we describe the generation of transgenic V. vinifera lines constitutively expressing the V. riparia E3 ubiquitin ligase gene VriATL156. Phenotypic and molecular analysis revealed that the transgenic plants were less susceptible to P. viticola than vector-only controls, confirming the role of this E3 ubiquitin ligase in the innate immune response. Two independent transgenic lines were selected for detailed analysis of the resistance phenotype by RNA-Seq and microscopy, revealing the profound reprogramming of transcription to achieve resistance that operates from the earliest stages of pathogen infection. The introduction of VriATL156 into elite grapevine cultivars could therefore provide an effective and sustainable control measure against downy mildew.
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spelling pubmed-78334272021-01-26 The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola Vandelle, Elodie Ariani, Pietro Regaiolo, Alice Danzi, Davide Lovato, Arianna Zadra, Claudia Vitulo, Nicola Gambino, Giorgio Polverari, Annalisa Int J Mol Sci Article Downy mildew, caused by Plasmopara viticola, is one of the most severe diseases of grapevine (Vitis vinifera L.). Genetic resistance is an effective and sustainable control strategy, but major resistance genes (encoding receptors for specific pathogen effectors) introgressed from wild Vitis species, although effective, may be non-durable because the pathogen can evolve to avoid specific recognition. Previous transcriptomic studies in the resistant species Vitis riparia highlighted the activation of signal transduction components during infection. The transfer of such components to V. vinifera might confer less specific and therefore more durable resistance. Here, we describe the generation of transgenic V. vinifera lines constitutively expressing the V. riparia E3 ubiquitin ligase gene VriATL156. Phenotypic and molecular analysis revealed that the transgenic plants were less susceptible to P. viticola than vector-only controls, confirming the role of this E3 ubiquitin ligase in the innate immune response. Two independent transgenic lines were selected for detailed analysis of the resistance phenotype by RNA-Seq and microscopy, revealing the profound reprogramming of transcription to achieve resistance that operates from the earliest stages of pathogen infection. The introduction of VriATL156 into elite grapevine cultivars could therefore provide an effective and sustainable control measure against downy mildew. MDPI 2021-01-19 /pmc/articles/PMC7833427/ /pubmed/33477914 http://dx.doi.org/10.3390/ijms22020940 Text en © 2021 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
Vandelle, Elodie
Ariani, Pietro
Regaiolo, Alice
Danzi, Davide
Lovato, Arianna
Zadra, Claudia
Vitulo, Nicola
Gambino, Giorgio
Polverari, Annalisa
The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola
title The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola
title_full The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola
title_fullStr The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola
title_full_unstemmed The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola
title_short The Grapevine E3 Ubiquitin Ligase VriATL156 Confers Resistance against the Downy Mildew Pathogen Plasmopara viticola
title_sort grapevine e3 ubiquitin ligase vriatl156 confers resistance against the downy mildew pathogen plasmopara viticola
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833427/
https://www.ncbi.nlm.nih.gov/pubmed/33477914
http://dx.doi.org/10.3390/ijms22020940
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