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A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection

Fungicides are applied intensively to prevent downy mildew infections of grapevines (Vitis vinifera) with high impact on the environment. In order to develop alternative strategies we sequenced the genome of the oomycete pathogen Plasmopara viticola causing this disease. We show that it derives from...

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Autores principales: Brilli, Matteo, Asquini, Elisa, Moser, Mirko, Bianchedi, Pier Luigi, Perazzolli, Michele, Si-Ammour, Azeddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768699/
https://www.ncbi.nlm.nih.gov/pubmed/29335535
http://dx.doi.org/10.1038/s41598-018-19158-8
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author Brilli, Matteo
Asquini, Elisa
Moser, Mirko
Bianchedi, Pier Luigi
Perazzolli, Michele
Si-Ammour, Azeddine
author_facet Brilli, Matteo
Asquini, Elisa
Moser, Mirko
Bianchedi, Pier Luigi
Perazzolli, Michele
Si-Ammour, Azeddine
author_sort Brilli, Matteo
collection PubMed
description Fungicides are applied intensively to prevent downy mildew infections of grapevines (Vitis vinifera) with high impact on the environment. In order to develop alternative strategies we sequenced the genome of the oomycete pathogen Plasmopara viticola causing this disease. We show that it derives from a Phytophthora-like ancestor that switched to obligate biotrophy by losing genes involved in nitrogen metabolism and γ-Aminobutyric acid catabolism. By combining multiple omics approaches we characterized the pathosystem and identified a RxLR effector that trigger an immune response in the wild species V. riparia. This effector is an ideal marker to screen novel grape resistant varieties. Our study reveals an unprecedented bidirectional noncoding RNA-based mechanism that, in one direction might be fundamental for P. viticola to proficiently infect its host, and in the other might reduce the effects of the infection on the plant.
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spelling pubmed-57686992018-01-25 A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection Brilli, Matteo Asquini, Elisa Moser, Mirko Bianchedi, Pier Luigi Perazzolli, Michele Si-Ammour, Azeddine Sci Rep Article Fungicides are applied intensively to prevent downy mildew infections of grapevines (Vitis vinifera) with high impact on the environment. In order to develop alternative strategies we sequenced the genome of the oomycete pathogen Plasmopara viticola causing this disease. We show that it derives from a Phytophthora-like ancestor that switched to obligate biotrophy by losing genes involved in nitrogen metabolism and γ-Aminobutyric acid catabolism. By combining multiple omics approaches we characterized the pathosystem and identified a RxLR effector that trigger an immune response in the wild species V. riparia. This effector is an ideal marker to screen novel grape resistant varieties. Our study reveals an unprecedented bidirectional noncoding RNA-based mechanism that, in one direction might be fundamental for P. viticola to proficiently infect its host, and in the other might reduce the effects of the infection on the plant. Nature Publishing Group UK 2018-01-15 /pmc/articles/PMC5768699/ /pubmed/29335535 http://dx.doi.org/10.1038/s41598-018-19158-8 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Brilli, Matteo
Asquini, Elisa
Moser, Mirko
Bianchedi, Pier Luigi
Perazzolli, Michele
Si-Ammour, Azeddine
A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
title A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
title_full A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
title_fullStr A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
title_full_unstemmed A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
title_short A multi-omics study of the grapevine-downy mildew (Plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
title_sort multi-omics study of the grapevine-downy mildew (plasmopara viticola) pathosystem unveils a complex protein coding- and noncoding-based arms race during infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768699/
https://www.ncbi.nlm.nih.gov/pubmed/29335535
http://dx.doi.org/10.1038/s41598-018-19158-8
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