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Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control
A multitude of resistance deployment strategies have been proposed to tackle the evolutionary potential of pathogens to overcome plant resistance. In particular, many landscape‐based strategies rely on the deployment of resistant and susceptible cultivars in an agricultural landscape as a mosaic. Ho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979631/ https://www.ncbi.nlm.nih.gov/pubmed/29875812 http://dx.doi.org/10.1111/eva.12570 |
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author | Papaïx, Julien Rimbaud, Loup Burdon, Jeremy J. Zhan, Jiasui Thrall, Peter H. |
author_facet | Papaïx, Julien Rimbaud, Loup Burdon, Jeremy J. Zhan, Jiasui Thrall, Peter H. |
author_sort | Papaïx, Julien |
collection | PubMed |
description | A multitude of resistance deployment strategies have been proposed to tackle the evolutionary potential of pathogens to overcome plant resistance. In particular, many landscape‐based strategies rely on the deployment of resistant and susceptible cultivars in an agricultural landscape as a mosaic. However, the design of such strategies is not easy as strategies targeting epidemiological or evolutionary outcomes may not be the same. Using a stochastic spatially explicit model, we studied the impact of landscape organization (as defined by the proportion of fields cultivated with a resistant cultivar and their spatial aggregation) and key pathogen life‐history traits on three measures of disease control. Our results show that short‐term epidemiological dynamics are optimized when landscapes are planted with a high proportion of the resistant cultivar in low aggregation. Importantly, the exact opposite situation is optimal for resistance durability. Finally, well‐mixed landscapes (balanced proportions with low aggregation) are optimal for long‐term evolutionary equilibrium (defined here as the level of long‐term pathogen adaptation). This work offers a perspective on the potential for contrasting effects of landscape organization on different goals of disease management and highlights the role of pathogen life history. |
format | Online Article Text |
id | pubmed-5979631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59796312018-06-06 Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control Papaïx, Julien Rimbaud, Loup Burdon, Jeremy J. Zhan, Jiasui Thrall, Peter H. Evol Appl Original Articles A multitude of resistance deployment strategies have been proposed to tackle the evolutionary potential of pathogens to overcome plant resistance. In particular, many landscape‐based strategies rely on the deployment of resistant and susceptible cultivars in an agricultural landscape as a mosaic. However, the design of such strategies is not easy as strategies targeting epidemiological or evolutionary outcomes may not be the same. Using a stochastic spatially explicit model, we studied the impact of landscape organization (as defined by the proportion of fields cultivated with a resistant cultivar and their spatial aggregation) and key pathogen life‐history traits on three measures of disease control. Our results show that short‐term epidemiological dynamics are optimized when landscapes are planted with a high proportion of the resistant cultivar in low aggregation. Importantly, the exact opposite situation is optimal for resistance durability. Finally, well‐mixed landscapes (balanced proportions with low aggregation) are optimal for long‐term evolutionary equilibrium (defined here as the level of long‐term pathogen adaptation). This work offers a perspective on the potential for contrasting effects of landscape organization on different goals of disease management and highlights the role of pathogen life history. John Wiley and Sons Inc. 2017-11-30 /pmc/articles/PMC5979631/ /pubmed/29875812 http://dx.doi.org/10.1111/eva.12570 Text en © 2017 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Papaïx, Julien Rimbaud, Loup Burdon, Jeremy J. Zhan, Jiasui Thrall, Peter H. Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
title | Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
title_full | Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
title_fullStr | Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
title_full_unstemmed | Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
title_short | Differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
title_sort | differential impact of landscape‐scale strategies for crop cultivar deployment on disease dynamics, resistance durability and long‐term evolutionary control |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979631/ https://www.ncbi.nlm.nih.gov/pubmed/29875812 http://dx.doi.org/10.1111/eva.12570 |
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