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Antifungal alternation can be beneficial for durability but at the cost of generalist resistance
The evolution of resistance to pesticides is a major burden in agriculture. Resistance management involves maximizing selection pressure heterogeneity, particularly by combining active ingredients with different modes of action. We tested the hypothesis that alternation may delay the build-up of res...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935548/ https://www.ncbi.nlm.nih.gov/pubmed/36797413 http://dx.doi.org/10.1038/s42003-023-04550-6 |
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author | Ballu, Agathe Despréaux, Philomène Duplaix, Clémentine Dérédec, Anne Carpentier, Florence Walker, Anne-Sophie |
author_facet | Ballu, Agathe Despréaux, Philomène Duplaix, Clémentine Dérédec, Anne Carpentier, Florence Walker, Anne-Sophie |
author_sort | Ballu, Agathe |
collection | PubMed |
description | The evolution of resistance to pesticides is a major burden in agriculture. Resistance management involves maximizing selection pressure heterogeneity, particularly by combining active ingredients with different modes of action. We tested the hypothesis that alternation may delay the build-up of resistance not only by spreading selection pressure over longer periods, but also by decreasing the rate of evolution of resistance to alternated fungicides, by applying an experimental evolution approach to the economically important crop pathogen Zymoseptoria tritici. Our results show that alternation is either neutral or slows the overall resistance evolution rate, relative to continuous fungicide use, but results in higher levels of generalism in evolved lines. We demonstrate that the nature of the fungicides, and therefore their relative intrinsic risk of resistance may underly this trade-off, more so than the number of fungicides and the rhythm of alternation. This trade-off is also dynamic over the course of resistance evolution. These findings open up new possibilities for tailoring resistance management effectively while optimizing interplay between alternation components. |
format | Online Article Text |
id | pubmed-9935548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99355482023-02-18 Antifungal alternation can be beneficial for durability but at the cost of generalist resistance Ballu, Agathe Despréaux, Philomène Duplaix, Clémentine Dérédec, Anne Carpentier, Florence Walker, Anne-Sophie Commun Biol Article The evolution of resistance to pesticides is a major burden in agriculture. Resistance management involves maximizing selection pressure heterogeneity, particularly by combining active ingredients with different modes of action. We tested the hypothesis that alternation may delay the build-up of resistance not only by spreading selection pressure over longer periods, but also by decreasing the rate of evolution of resistance to alternated fungicides, by applying an experimental evolution approach to the economically important crop pathogen Zymoseptoria tritici. Our results show that alternation is either neutral or slows the overall resistance evolution rate, relative to continuous fungicide use, but results in higher levels of generalism in evolved lines. We demonstrate that the nature of the fungicides, and therefore their relative intrinsic risk of resistance may underly this trade-off, more so than the number of fungicides and the rhythm of alternation. This trade-off is also dynamic over the course of resistance evolution. These findings open up new possibilities for tailoring resistance management effectively while optimizing interplay between alternation components. Nature Publishing Group UK 2023-02-16 /pmc/articles/PMC9935548/ /pubmed/36797413 http://dx.doi.org/10.1038/s42003-023-04550-6 Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ballu, Agathe Despréaux, Philomène Duplaix, Clémentine Dérédec, Anne Carpentier, Florence Walker, Anne-Sophie Antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
title | Antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
title_full | Antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
title_fullStr | Antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
title_full_unstemmed | Antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
title_short | Antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
title_sort | antifungal alternation can be beneficial for durability but at the cost of generalist resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935548/ https://www.ncbi.nlm.nih.gov/pubmed/36797413 http://dx.doi.org/10.1038/s42003-023-04550-6 |
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