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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9304176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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
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title_full | Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
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title_fullStr | Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
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title_full_unstemmed | Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
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title_short | Sexual reproduction contributes to the evolution of resistance‐breaking isolates of the spinach pathogen Peronospora effusa
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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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