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Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance
BACKGROUND: Insecticide resistance is now common in insects due to the frequent use of chemicals to control them, which provides a useful tool to study the adaptation of eukaryotic genome to new environments. Although numerous potential mutations may provide high level of resistance, only few allele...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC362868/ https://www.ncbi.nlm.nih.gov/pubmed/15018650 http://dx.doi.org/10.1186/1471-2148-4-5 |
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author | Shi, Ming An Lougarre, Andrée Alies, Carole Frémaux, Isabelle Tang, Zhen Hua Stojan, Jure Fournier, Didier |
author_facet | Shi, Ming An Lougarre, Andrée Alies, Carole Frémaux, Isabelle Tang, Zhen Hua Stojan, Jure Fournier, Didier |
author_sort | Shi, Ming An |
collection | PubMed |
description | BACKGROUND: Insecticide resistance is now common in insects due to the frequent use of chemicals to control them, which provides a useful tool to study the adaptation of eukaryotic genome to new environments. Although numerous potential mutations may provide high level of resistance, only few alleles are found in insect natural populations. Then, we hypothesized that only alleles linked to the highest fitness in the absence of insecticide are selected. RESULTS: To obtain information on the origin of the fitness of resistant alleles, we studied Drosophila melanogaster acetylcholinesterase, the target of organophosphate and carbamate insecticides. We produced in vitro 15 possible proteins resulting from the combination of the four most frequent mutations and we tested their catalytic activity and enzymatic stability. Mutations affected deacetylation of the enzyme, decreasing or increasing its catalytic efficiency and all mutations diminished the stability of the enzyme. Combination of mutations result to an additive alteration. CONCLUSION: Our findings suggest that the alteration of activity and stability of acetylcholinesterase are at the origin of the fitness cost associated with mutations providing resistance. Magnitude of the alterations was related to the allelic frequency in Drosophila populations suggesting that the fitness cost is the main driving force for the maintenance of resistant alleles in insecticide free conditions. |
format | Text |
id | pubmed-362868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-3628682004-03-11 Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance Shi, Ming An Lougarre, Andrée Alies, Carole Frémaux, Isabelle Tang, Zhen Hua Stojan, Jure Fournier, Didier BMC Evol Biol Research Article BACKGROUND: Insecticide resistance is now common in insects due to the frequent use of chemicals to control them, which provides a useful tool to study the adaptation of eukaryotic genome to new environments. Although numerous potential mutations may provide high level of resistance, only few alleles are found in insect natural populations. Then, we hypothesized that only alleles linked to the highest fitness in the absence of insecticide are selected. RESULTS: To obtain information on the origin of the fitness of resistant alleles, we studied Drosophila melanogaster acetylcholinesterase, the target of organophosphate and carbamate insecticides. We produced in vitro 15 possible proteins resulting from the combination of the four most frequent mutations and we tested their catalytic activity and enzymatic stability. Mutations affected deacetylation of the enzyme, decreasing or increasing its catalytic efficiency and all mutations diminished the stability of the enzyme. Combination of mutations result to an additive alteration. CONCLUSION: Our findings suggest that the alteration of activity and stability of acetylcholinesterase are at the origin of the fitness cost associated with mutations providing resistance. Magnitude of the alterations was related to the allelic frequency in Drosophila populations suggesting that the fitness cost is the main driving force for the maintenance of resistant alleles in insecticide free conditions. BioMed Central 2004-02-06 /pmc/articles/PMC362868/ /pubmed/15018650 http://dx.doi.org/10.1186/1471-2148-4-5 Text en Copyright © 2004 Shi et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Shi, Ming An Lougarre, Andrée Alies, Carole Frémaux, Isabelle Tang, Zhen Hua Stojan, Jure Fournier, Didier Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
title | Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
title_full | Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
title_fullStr | Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
title_full_unstemmed | Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
title_short | Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
title_sort | acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC362868/ https://www.ncbi.nlm.nih.gov/pubmed/15018650 http://dx.doi.org/10.1186/1471-2148-4-5 |
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