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Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa

Peronospora effusa causes downy mildew, the economically most important disease of cultivated spinach worldwide. To date, 19 P. effusa races have been denominated based on their capacity to break spinach resistances, but their genetic diversity and the evolutionary processes that contribute to race...

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Autores principales: Skiadas, Petros, Klein, Joël, Quiroz‐Monnens, Thomas, Elberse, Joyce, de Jonge, Ronnie, Van den Ackerveken, Guido, Seidl, Michael F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304176/
https://www.ncbi.nlm.nih.gov/pubmed/35191594
http://dx.doi.org/10.1111/1462-2920.15944
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author Skiadas, Petros
Klein, Joël
Quiroz‐Monnens, Thomas
Elberse, Joyce
de Jonge, Ronnie
Van den Ackerveken, Guido
Seidl, Michael F.
author_facet Skiadas, Petros
Klein, Joël
Quiroz‐Monnens, Thomas
Elberse, Joyce
de Jonge, Ronnie
Van den Ackerveken, Guido
Seidl, Michael F.
author_sort Skiadas, Petros
collection PubMed
description Peronospora effusa causes downy mildew, the economically most important disease of cultivated spinach worldwide. To date, 19 P. effusa races have been denominated based on their capacity to break spinach resistances, but their genetic diversity and the evolutionary processes that contribute to race emergence are unknown. Here, we performed the first systematic analysis of P. effusa races showing that those emerge by both asexual and sexual reproduction. Specifically, we studied the diversity of 26 P. effusa isolates from 16 denominated races based on mitochondrial and nuclear comparative genomics. Mitochondrial genomes based on long‐read sequencing coupled with diversity assessment based on short‐read sequencing uncovered two mitochondrial haplogroups, each with distinct genome organization. Nuclear genome‐wide comparisons of the 26 isolates revealed that 10 isolates from six races could clearly be divided into three asexually evolving groups, in concordance with their mitochondrial phylogeny. The remaining isolates showed signals of reticulated evolution and discordance between nuclear and mitochondrial phylogenies, suggesting that these evolved through sexual reproduction. Increased understanding of this pathogen's reproductive modes will provide the framework for future studies into the molecular mechanisms underlying race emergence and into the P. effusa‐spinach interaction, thus assisting in sustainable production of spinach through knowledge‐driven resistance breeding.
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spelling pubmed-93041762022-07-28 Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa Skiadas, Petros Klein, Joël Quiroz‐Monnens, Thomas Elberse, Joyce de Jonge, Ronnie Van den Ackerveken, Guido Seidl, Michael F. Environ Microbiol Special Issue Articles Peronospora effusa causes downy mildew, the economically most important disease of cultivated spinach worldwide. To date, 19 P. effusa races have been denominated based on their capacity to break spinach resistances, but their genetic diversity and the evolutionary processes that contribute to race emergence are unknown. Here, we performed the first systematic analysis of P. effusa races showing that those emerge by both asexual and sexual reproduction. Specifically, we studied the diversity of 26 P. effusa isolates from 16 denominated races based on mitochondrial and nuclear comparative genomics. Mitochondrial genomes based on long‐read sequencing coupled with diversity assessment based on short‐read sequencing uncovered two mitochondrial haplogroups, each with distinct genome organization. Nuclear genome‐wide comparisons of the 26 isolates revealed that 10 isolates from six races could clearly be divided into three asexually evolving groups, in concordance with their mitochondrial phylogeny. The remaining isolates showed signals of reticulated evolution and discordance between nuclear and mitochondrial phylogenies, suggesting that these evolved through sexual reproduction. Increased understanding of this pathogen's reproductive modes will provide the framework for future studies into the molecular mechanisms underlying race emergence and into the P. effusa‐spinach interaction, thus assisting in sustainable production of spinach through knowledge‐driven resistance breeding. John Wiley & Sons, Inc. 2022-02-28 2022-03 /pmc/articles/PMC9304176/ /pubmed/35191594 http://dx.doi.org/10.1111/1462-2920.15944 Text en © 2022 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Issue Articles
Skiadas, Petros
Klein, Joël
Quiroz‐Monnens, Thomas
Elberse, Joyce
de Jonge, Ronnie
Van den Ackerveken, Guido
Seidl, Michael F.
Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
title Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
title_full Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
title_fullStr Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
title_full_unstemmed Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
title_short Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
title_sort sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen peronospora effusa
topic Special Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304176/
https://www.ncbi.nlm.nih.gov/pubmed/35191594
http://dx.doi.org/10.1111/1462-2920.15944
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