Delaying quantitative resistance to pesticides and antibiotics

Abstract 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...

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Main Author: Nate B. Hardy
Format: Article
Language:English
Published: Wiley 2022-12-01
Series:Evolutionary Applications
Subjects:
Online Access:https://doi.org/10.1111/eva.13497
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author Nate B. Hardy
author_facet Nate B. Hardy
author_sort Nate B. Hardy
collection DOAJ
description Abstract 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.
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spelling doaj.art-dfb7f33f41394c1a874a6b7f12f2ccd22022-12-22T04:41:47ZengWileyEvolutionary Applications1752-45712022-12-0115122067207710.1111/eva.13497Delaying quantitative resistance to pesticides and antibioticsNate B. Hardy0Department of Entomology and Plant Pathology Auburn University Auburn Alabama USAAbstract 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.https://doi.org/10.1111/eva.13497antimicrobial resistanceinsecticide resistancepopulation geneticsquantitative geneticsR‐genes
spellingShingle Nate B. Hardy
Delaying quantitative resistance to pesticides and antibiotics
Evolutionary Applications
antimicrobial resistance
insecticide resistance
population genetics
quantitative genetics
R‐genes
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 antimicrobial resistance
insecticide resistance
population genetics
quantitative genetics
R‐genes
url https://doi.org/10.1111/eva.13497
work_keys_str_mv AT natebhardy delayingquantitativeresistancetopesticidesandantibiotics