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An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito

Widespread resistance to pyrethroids threatens malaria control in Africa. Consequently, several countries switched to carbamates and organophophates insecticides for indoor residual spraying. However, a mutation in the ace-1 gene conferring resistance to these compounds (ace-1(R) allele), is already...

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Autores principales: Assogba, Benoît S., Djogbénou, Luc S., Milesi, Pascal, Berthomieu, Arnaud, Perez, Julie, Ayala, Diego, Chandre, Fabrice, Makoutodé, Michel, Labbé, Pierrick, Weill, Mylène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592963/
https://www.ncbi.nlm.nih.gov/pubmed/26434951
http://dx.doi.org/10.1038/srep14529
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author Assogba, Benoît S.
Djogbénou, Luc S.
Milesi, Pascal
Berthomieu, Arnaud
Perez, Julie
Ayala, Diego
Chandre, Fabrice
Makoutodé, Michel
Labbé, Pierrick
Weill, Mylène
author_facet Assogba, Benoît S.
Djogbénou, Luc S.
Milesi, Pascal
Berthomieu, Arnaud
Perez, Julie
Ayala, Diego
Chandre, Fabrice
Makoutodé, Michel
Labbé, Pierrick
Weill, Mylène
author_sort Assogba, Benoît S.
collection PubMed
description Widespread resistance to pyrethroids threatens malaria control in Africa. Consequently, several countries switched to carbamates and organophophates insecticides for indoor residual spraying. However, a mutation in the ace-1 gene conferring resistance to these compounds (ace-1(R) allele), is already present. Furthermore, a duplicated allele (ace-1(D)) recently appeared; characterizing its selective advantage is mandatory to evaluate the threat. Our data revealed that a unique duplication event, pairing a susceptible and a resistant copy of the ace-1 gene spread through West Africa. Further investigations revealed that, while ace-1(D) confers less resistance than ace-1(R), the high fitness cost associated with ace-1(R) is almost completely suppressed by the duplication for all traits studied. ace-1 duplication thus represents a permanent heterozygote phenotype, selected, and thus spreading, due to the mosaic nature of mosquito control. It provides malaria mosquito with a new evolutionary path that could hamper resistance management.
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spelling pubmed-45929632015-10-19 An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito Assogba, Benoît S. Djogbénou, Luc S. Milesi, Pascal Berthomieu, Arnaud Perez, Julie Ayala, Diego Chandre, Fabrice Makoutodé, Michel Labbé, Pierrick Weill, Mylène Sci Rep Article Widespread resistance to pyrethroids threatens malaria control in Africa. Consequently, several countries switched to carbamates and organophophates insecticides for indoor residual spraying. However, a mutation in the ace-1 gene conferring resistance to these compounds (ace-1(R) allele), is already present. Furthermore, a duplicated allele (ace-1(D)) recently appeared; characterizing its selective advantage is mandatory to evaluate the threat. Our data revealed that a unique duplication event, pairing a susceptible and a resistant copy of the ace-1 gene spread through West Africa. Further investigations revealed that, while ace-1(D) confers less resistance than ace-1(R), the high fitness cost associated with ace-1(R) is almost completely suppressed by the duplication for all traits studied. ace-1 duplication thus represents a permanent heterozygote phenotype, selected, and thus spreading, due to the mosaic nature of mosquito control. It provides malaria mosquito with a new evolutionary path that could hamper resistance management. Nature Publishing Group 2015-10-05 /pmc/articles/PMC4592963/ /pubmed/26434951 http://dx.doi.org/10.1038/srep14529 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Assogba, Benoît S.
Djogbénou, Luc S.
Milesi, Pascal
Berthomieu, Arnaud
Perez, Julie
Ayala, Diego
Chandre, Fabrice
Makoutodé, Michel
Labbé, Pierrick
Weill, Mylène
An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito
title An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito
title_full An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito
title_fullStr An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito
title_full_unstemmed An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito
title_short An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito
title_sort ace-1 gene duplication resorbs the fitness cost associated with resistance in anopheles gambiae, the main malaria mosquito
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592963/
https://www.ncbi.nlm.nih.gov/pubmed/26434951
http://dx.doi.org/10.1038/srep14529
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