Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance

<p>Abstract</p> <p>Background</p> <p>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 mutation...

Full description

Bibliographic Details
Main Authors: Tang Zhen, Frémaux Isabelle, Alies Carole, Lougarre Andrée, Shi Ming, Stojan Jure, Fournier Didier
Format: Article
Language:English
Published: BMC 2004-02-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/4/5
_version_ 1811191150894120960
author Tang Zhen
Frémaux Isabelle
Alies Carole
Lougarre Andrée
Shi Ming
Stojan Jure
Fournier Didier
author_facet Tang Zhen
Frémaux Isabelle
Alies Carole
Lougarre Andrée
Shi Ming
Stojan Jure
Fournier Didier
author_sort Tang Zhen
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>To obtain information on the origin of the fitness of resistant alleles, we studied <it>Drosophila melanogaster </it>acetylcholinesterase, the target of organophosphate and carbamate insecticides. We produced <it>in vitro </it>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.</p> <p>Conclusion</p> <p>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 <it>Drosophila </it>populations suggesting that the fitness cost is the main driving force for the maintenance of resistant alleles in insecticide free conditions.</p>
first_indexed 2024-04-11T15:01:52Z
format Article
id doaj.art-9ad5b9594d5d4472b64c09578ebee03f
institution Directory Open Access Journal
issn 1471-2148
language English
last_indexed 2024-04-11T15:01:52Z
publishDate 2004-02-01
publisher BMC
record_format Article
series BMC Evolutionary Biology
spelling doaj.art-9ad5b9594d5d4472b64c09578ebee03f2022-12-22T04:16:56ZengBMCBMC Evolutionary Biology1471-21482004-02-0141510.1186/1471-2148-4-5Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistanceTang ZhenFrémaux IsabelleAlies CaroleLougarre AndréeShi MingStojan JureFournier Didier<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>To obtain information on the origin of the fitness of resistant alleles, we studied <it>Drosophila melanogaster </it>acetylcholinesterase, the target of organophosphate and carbamate insecticides. We produced <it>in vitro </it>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.</p> <p>Conclusion</p> <p>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 <it>Drosophila </it>populations suggesting that the fitness cost is the main driving force for the maintenance of resistant alleles in insecticide free conditions.</p>http://www.biomedcentral.com/1471-2148/4/5
spellingShingle Tang Zhen
Frémaux Isabelle
Alies Carole
Lougarre Andrée
Shi Ming
Stojan Jure
Fournier Didier
Acetylcholinesterase alterations reveal the fitness cost of mutations conferring insecticide resistance
BMC Evolutionary Biology
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
url http://www.biomedcentral.com/1471-2148/4/5
work_keys_str_mv AT tangzhen acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance
AT fremauxisabelle acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance
AT aliescarole acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance
AT lougarreandree acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance
AT shiming acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance
AT stojanjure acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance
AT fournierdidier acetylcholinesterasealterationsrevealthefitnesscostofmutationsconferringinsecticideresistance