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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...

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Autores principales: Shi, Ming An, Lougarre, Andrée, Alies, Carole, Frémaux, Isabelle, Tang, Zhen Hua, Stojan, Jure, Fournier, Didier
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
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.
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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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