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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7496652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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
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title_full | Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
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title_fullStr | Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
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title_full_unstemmed | Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
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title_short | Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
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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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