Identifying genomic changes associated with insecticide resistance in the dengue mosquito Aedes aegypti by deep targeted sequencing

  1. Jean-Philippe David1,2,3
  1. 1Laboratoire d'Ecologie Alpine (LECA), CNRS, UMR 5553, 38041 Grenoble Cedex 9, France;
  2. 2Université Grenoble–Alpes, 38041 Grenoble Cedex 9, France;
  3. 3Environmental and Systems Biology (BEeSy), Université Grenoble–Alpes, 38041 Grenoble Cedex 9, France;
  4. 4Unité d'Entomologie Médicale, Institut Pasteur de la Guyane, 97306 Cayenne Cedex, France;
  5. 5Pôle Rhône Alpes de Bioinformatique, Université Lyon 1, 69100 Villeurbanne, France;
  6. 6Institut de Recherche pour le Développement (IRD), Maladies Infectieuses et Vecteurs, Ecologie, Génétique, Evolution et Contrôle (IRD 224-CNRS 5290 UM1-UM2), 34394 Montpellier Cedex 5, France;
  7. 7Department of Entomology, Faculty of Agriculture, Kasetsart University, Lat Yao Chatuchak Bangkok 10900, Thailand;
  8. 8Center for Advanced Studies for Agriculture and Food, Kasetsart University Institute for Advanced Studies, Kasetsart University, Bangkok 10900, Thailand (CASAF, NRU-KU, Thailand);
  9. 9Bureau of Vector Borne Diseases, Department of Disease Control, Ministry of Public Health, Mueang, Nonthaburi 11000, Thailand;
  10. 10Vector Biology Group, Liverpool School of Tropical Medicine, L35QA Liverpool, United Kingdom
  1. Corresponding author: jean-philippe.david{at}ujf-grenoble.fr

Abstract

The capacity of mosquitoes to resist insecticides threatens the control of diseases such as dengue and malaria. Until alternative control tools are implemented, characterizing resistance mechanisms is crucial for managing resistance in natural populations. Insecticide biodegradation by detoxification enzymes is a common resistance mechanism; however, the genomic changes underlying this mechanism have rarely been identified, precluding individual resistance genotyping. In particular, the role of copy number variations (CNVs) and polymorphisms of detoxification enzymes have never been investigated at the genome level, although they can represent robust markers of metabolic resistance. In this context, we combined target enrichment with high-throughput sequencing for conducting the first comprehensive screening of gene amplifications and polymorphisms associated with insecticide resistance in mosquitoes. More than 760 candidate genes were captured and deep sequenced in several populations of the dengue mosquito Ae. aegypti displaying distinct genetic backgrounds and contrasted resistance levels to the insecticide deltamethrin. CNV analysis identified 41 gene amplifications associated with resistance, most affecting cytochrome P450s overtranscribed in resistant populations. Polymorphism analysis detected more than 30,000 variants and strong selection footprints in specific genomic regions. Combining Bayesian and allele frequency filtering approaches identified 55 nonsynonymous variants strongly associated with resistance. Both CNVs and polymorphisms were conserved within regions but differed across continents, confirming that genomic changes underlying metabolic resistance to insecticides are not universal. By identifying novel DNA markers of insecticide resistance, this study opens the way for tracking down metabolic changes developed by mosquitoes to resist insecticides within and among populations.

Footnotes

  • [Supplemental material is available for this article.]

  • Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.189225.115.

  • Freely available online through the Genome Research Open Access option.

  • Received January 5, 2015.
  • Accepted June 30, 2015.

This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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