4.6 Article

A genomic amplification affecting a carboxylesterase gene cluster confers organophosphate resistance in the mosquito Aedes aegypti: From genomic characterization to high-throughput field detection

Journal

EVOLUTIONARY APPLICATIONS
Volume 14, Issue 4, Pages 1009-1022

Publisher

WILEY
DOI: 10.1111/eva.13177

Keywords

Aedes aegypti; carboxylesterase; diagnostic assay; genomic amplification; insecticide resistance; mosquito

Funding

  1. European Union's Horizon 2020 research and innovation programme [731060, 734548]
  2. AFD (Agence Francaise pour le Developpement)
  3. U.S. Naval Medical Research Unit

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Genomic amplifications can be a key component of short-term adaptive processes by altering gene expression and creating paralogs. Insects exposed to insecticides may develop gene amplifications that increase the expression of detoxification enzymes, which can be monitored using DNA markers. This study identified a genomic amplification event associated with resistance to organophosphate insecticides in Aedes aegypti and developed a molecular assay to monitor resistance alleles in the field, revealing a trade-off between resistance mechanisms and fitness costs.
By altering gene expression and creating paralogs, genomic amplifications represent a key component of short-term adaptive processes. In insects, the use of insecticides can select gene amplifications causing an increased expression of detoxification enzymes, supporting the usefulness of these DNA markers for monitoring the dynamics of resistance alleles in the field. In this context, the present study aims to characterize a genomic amplification event associated with resistance to organophosphate insecticides in the mosquito Aedes aegypti and to develop a molecular assay to monitor the associated resistance alleles in the field. An experimental evolution experiment using a composite population from Laos supported the association between the over-transcription of multiple contiguous carboxylesterase genes on chromosome 2 and resistance to multiple organophosphate insecticides. Combining whole genome sequencing and qPCR on specific genes confirmed the presence of a similar to 100-Kb amplification spanning at least five carboxylesterase genes at this locus with the co-existence of multiple structural duplication haplotypes. Field data confirmed their circulation in South-East Asia and revealed high copy number polymorphism among and within populations suggesting a trade-off between this resistance mechanism and associated fitness costs. A dual-color multiplex TaqMan assay allowing the rapid detection and copy number quantification of this amplification event in Ae. aegypti was developed and validated on field populations. The routine use of this novel assay will improve the tracking of resistance alleles in this major arbovirus vector.

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