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Delaying quantitative resistance to pesticides and antibiotics
How can we best vary the application of pesticides and antibiotics to delay resistance evolution? Previous theoretical comparisons of deployment strategies have focused on qualitative resistance traits and have mostly assumed that resistance alleles are already present in a population. But many real...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753825/ https://www.ncbi.nlm.nih.gov/pubmed/36540637 http://dx.doi.org/10.1111/eva.13497 |
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author | Hardy, Nate B. |
author_facet | Hardy, Nate B. |
author_sort | Hardy, Nate B. |
collection | PubMed |
description | How can we best vary the application of pesticides and antibiotics to delay resistance evolution? Previous theoretical comparisons of deployment strategies have focused on qualitative resistance traits and have mostly assumed that resistance alleles are already present in a population. But many real resistance traits are quantitative, and the evolution of resistant genotypes in the field may depend on de novo mutation and recombination. Here, I use an individual‐based, forward‐time, quantitative‐genetic simulation model to investigate the evolution of quantitative resistance. I evaluate the performance of four application strategies for delaying resistance evolution, to wit, the (1) sequential, (2) mosaic, (3) periodic, and (4) combined strategies. I find that which strategy is best depends on initial efficacy. When at the onset, xenobiotics completely prevent reproduction in treated demes, a combined strategy is best. On the other hand, when populations are partially resistant, the combined strategy is inferior to mosaic and periodic strategies, especially when resistance alleles are antagonistically pleiotropic. Thus, the optimal application strategy for managing against the rise of quantitative resistance depends on pleiotropy and whether or not partial resistance is already present in a population. This result appears robust to variation in pest reproductive mode and migration rate, direct fitness costs for resistant phenotypes, and the extent of refugial habitats. |
format | Online Article Text |
id | pubmed-9753825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97538252022-12-19 Delaying quantitative resistance to pesticides and antibiotics Hardy, Nate B. Evol Appl Original Articles How can we best vary the application of pesticides and antibiotics to delay resistance evolution? Previous theoretical comparisons of deployment strategies have focused on qualitative resistance traits and have mostly assumed that resistance alleles are already present in a population. But many real resistance traits are quantitative, and the evolution of resistant genotypes in the field may depend on de novo mutation and recombination. Here, I use an individual‐based, forward‐time, quantitative‐genetic simulation model to investigate the evolution of quantitative resistance. I evaluate the performance of four application strategies for delaying resistance evolution, to wit, the (1) sequential, (2) mosaic, (3) periodic, and (4) combined strategies. I find that which strategy is best depends on initial efficacy. When at the onset, xenobiotics completely prevent reproduction in treated demes, a combined strategy is best. On the other hand, when populations are partially resistant, the combined strategy is inferior to mosaic and periodic strategies, especially when resistance alleles are antagonistically pleiotropic. Thus, the optimal application strategy for managing against the rise of quantitative resistance depends on pleiotropy and whether or not partial resistance is already present in a population. This result appears robust to variation in pest reproductive mode and migration rate, direct fitness costs for resistant phenotypes, and the extent of refugial habitats. John Wiley and Sons Inc. 2022-10-25 /pmc/articles/PMC9753825/ /pubmed/36540637 http://dx.doi.org/10.1111/eva.13497 Text en © 2022 The Author. Evolutionary Applications published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Hardy, Nate B. Delaying quantitative resistance to pesticides and antibiotics |
title | Delaying quantitative resistance to pesticides and antibiotics |
title_full | Delaying quantitative resistance to pesticides and antibiotics |
title_fullStr | Delaying quantitative resistance to pesticides and antibiotics |
title_full_unstemmed | Delaying quantitative resistance to pesticides and antibiotics |
title_short | Delaying quantitative resistance to pesticides and antibiotics |
title_sort | delaying quantitative resistance to pesticides and antibiotics |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753825/ https://www.ncbi.nlm.nih.gov/pubmed/36540637 http://dx.doi.org/10.1111/eva.13497 |
work_keys_str_mv | AT hardynateb delayingquantitativeresistancetopesticidesandantibiotics |