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An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts

Plasmopara viticola, an obligate biotrophic oomycete, is the causal agent of one of the most harmful grapevine diseases, downy mildew. Within this pathosystem, much information is gathered on the host, as characterization of pathogenicity and infection strategy of a biotrophic pathogen is quite chal...

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Autores principales: Figueiredo, Joana, Santos, Rita B., Guerra-Guimarães, Leonor, Leclercq, Céline C., Renaut, Jenny, Malhó, Rui, Figueiredo, Andreia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715676/
https://www.ncbi.nlm.nih.gov/pubmed/36456634
http://dx.doi.org/10.1038/s41598-022-25164-8
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author Figueiredo, Joana
Santos, Rita B.
Guerra-Guimarães, Leonor
Leclercq, Céline C.
Renaut, Jenny
Malhó, Rui
Figueiredo, Andreia
author_facet Figueiredo, Joana
Santos, Rita B.
Guerra-Guimarães, Leonor
Leclercq, Céline C.
Renaut, Jenny
Malhó, Rui
Figueiredo, Andreia
author_sort Figueiredo, Joana
collection PubMed
description Plasmopara viticola, an obligate biotrophic oomycete, is the causal agent of one of the most harmful grapevine diseases, downy mildew. Within this pathosystem, much information is gathered on the host, as characterization of pathogenicity and infection strategy of a biotrophic pathogen is quite challenging. Molecular insights into P. viticola development and pathogenicity are just beginning to be uncovered, mainly by transcriptomic studies. Plasmopara viticola proteome and secretome were only predicted based on transcriptome data. In this study, we have identified the in-planta proteome of P. viticola during infection of a susceptible (‘Trincadeira’) and a Rpv3-mediated resistance (‘Regent’) grapevine cultivar. Four hundred and twenty P. viticola proteins were identified on a label-free mass spectrometry-based approach of the apoplastic fluid of grapevine leaves. Overall, our study suggests that, in the compatible interaction, P. viticola manipulates salicylic-acid pathway and isoprenoid biosynthesis to enhance plant colonization. Furthermore, during the incompatible interaction, development-associated proteins increased while oxidoreductases protect P. viticola from ROS-associated plant defence mechanism. Up to our knowledge this is the first in-planta proteome characterization of this biotrophic pathogen, thus this study will open new insights into our understanding of this pathogen colonization strategy of both susceptible and Rpv3-mediated resistance grapevine genotypes.
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spelling pubmed-97156762022-12-03 An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts Figueiredo, Joana Santos, Rita B. Guerra-Guimarães, Leonor Leclercq, Céline C. Renaut, Jenny Malhó, Rui Figueiredo, Andreia Sci Rep Article Plasmopara viticola, an obligate biotrophic oomycete, is the causal agent of one of the most harmful grapevine diseases, downy mildew. Within this pathosystem, much information is gathered on the host, as characterization of pathogenicity and infection strategy of a biotrophic pathogen is quite challenging. Molecular insights into P. viticola development and pathogenicity are just beginning to be uncovered, mainly by transcriptomic studies. Plasmopara viticola proteome and secretome were only predicted based on transcriptome data. In this study, we have identified the in-planta proteome of P. viticola during infection of a susceptible (‘Trincadeira’) and a Rpv3-mediated resistance (‘Regent’) grapevine cultivar. Four hundred and twenty P. viticola proteins were identified on a label-free mass spectrometry-based approach of the apoplastic fluid of grapevine leaves. Overall, our study suggests that, in the compatible interaction, P. viticola manipulates salicylic-acid pathway and isoprenoid biosynthesis to enhance plant colonization. Furthermore, during the incompatible interaction, development-associated proteins increased while oxidoreductases protect P. viticola from ROS-associated plant defence mechanism. Up to our knowledge this is the first in-planta proteome characterization of this biotrophic pathogen, thus this study will open new insights into our understanding of this pathogen colonization strategy of both susceptible and Rpv3-mediated resistance grapevine genotypes. Nature Publishing Group UK 2022-12-01 /pmc/articles/PMC9715676/ /pubmed/36456634 http://dx.doi.org/10.1038/s41598-022-25164-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Figueiredo, Joana
Santos, Rita B.
Guerra-Guimarães, Leonor
Leclercq, Céline C.
Renaut, Jenny
Malhó, Rui
Figueiredo, Andreia
An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts
title An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts
title_full An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts
title_fullStr An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts
title_full_unstemmed An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts
title_short An in-planta comparative study of Plasmopara viticola proteome reveals different infection strategies towards susceptible and Rpv3-mediated resistance hosts
title_sort in-planta comparative study of plasmopara viticola proteome reveals different infection strategies towards susceptible and rpv3-mediated resistance hosts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715676/
https://www.ncbi.nlm.nih.gov/pubmed/36456634
http://dx.doi.org/10.1038/s41598-022-25164-8
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