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Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster

The evolution of resistance to drugs and pesticides poses a major threat to human health and food security. Neonicotinoids are highly effective insecticides used to control agricultural pests. They target the insect nicotinic acetylcholine receptor and mutations of the receptor that confer resistanc...

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Autores principales: Homem, Rafael A., Buttery, Bliss, Richardson, Ewan, Tan, Yao, Field, Linda M., Williamson, Martin S., Emyr Davies, T. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496652/
https://www.ncbi.nlm.nih.gov/pubmed/32510730
http://dx.doi.org/10.1111/mec.15503
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author Homem, Rafael A.
Buttery, Bliss
Richardson, Ewan
Tan, Yao
Field, Linda M.
Williamson, Martin S.
Emyr Davies, T. G.
author_facet Homem, Rafael A.
Buttery, Bliss
Richardson, Ewan
Tan, Yao
Field, Linda M.
Williamson, Martin S.
Emyr Davies, T. G.
author_sort Homem, Rafael A.
collection PubMed
description The evolution of resistance to drugs and pesticides poses a major threat to human health and food security. Neonicotinoids are highly effective insecticides used to control agricultural pests. They target the insect nicotinic acetylcholine receptor and mutations of the receptor that confer resistance have been slow to develop, with only one field‐evolved mutation being reported to date. This is an arginine‐to‐threonine substitution at position 81 of the nAChR_β1 subunit in neonicotinoid‐resistant aphids. To validate the role of R81T in neonicotinoid resistance and to test whether it may confer any significant fitness costs to insects, CRISPR/Cas9 was used to introduce an analogous mutation in the genome of Drosophila melanogaster. Flies carrying R81T showed an increased tolerance (resistance) to neonicotinoid insecticides, accompanied by a significant reduction in fitness. In comparison, flies carrying a deletion of the whole nAChR_α6 subunit, the target site of spinosyns, showed an increased tolerance to this class of insecticides but presented almost no fitness deficits.
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spelling pubmed-74966522020-09-25 Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster Homem, Rafael A. Buttery, Bliss Richardson, Ewan Tan, Yao Field, Linda M. Williamson, Martin S. Emyr Davies, T. G. Mol Ecol ORIGINAL ARTICLES The evolution of resistance to drugs and pesticides poses a major threat to human health and food security. Neonicotinoids are highly effective insecticides used to control agricultural pests. They target the insect nicotinic acetylcholine receptor and mutations of the receptor that confer resistance have been slow to develop, with only one field‐evolved mutation being reported to date. This is an arginine‐to‐threonine substitution at position 81 of the nAChR_β1 subunit in neonicotinoid‐resistant aphids. To validate the role of R81T in neonicotinoid resistance and to test whether it may confer any significant fitness costs to insects, CRISPR/Cas9 was used to introduce an analogous mutation in the genome of Drosophila melanogaster. Flies carrying R81T showed an increased tolerance (resistance) to neonicotinoid insecticides, accompanied by a significant reduction in fitness. In comparison, flies carrying a deletion of the whole nAChR_α6 subunit, the target site of spinosyns, showed an increased tolerance to this class of insecticides but presented almost no fitness deficits. John Wiley and Sons Inc. 2020-06-22 2020-07 /pmc/articles/PMC7496652/ /pubmed/32510730 http://dx.doi.org/10.1111/mec.15503 Text en © 2020 The Authors. Molecular Ecology 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
Homem, Rafael A.
Buttery, Bliss
Richardson, Ewan
Tan, Yao
Field, Linda M.
Williamson, Martin S.
Emyr Davies, T. G.
Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
title Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
title_full Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
title_fullStr Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
title_full_unstemmed Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
title_short Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
title_sort evolutionary trade‐offs of insecticide resistance — the fitness costs associated with target‐site mutations in the nachr of drosophila melanogaster
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496652/
https://www.ncbi.nlm.nih.gov/pubmed/32510730
http://dx.doi.org/10.1111/mec.15503
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