PT  - JOURNAL ARTICLE
AU  - Julien Cattel
AU  - Chloé Haberkorn
AU  - Fréderic Laporte
AU  - Thierry Gaude
AU  - Tristan Cumer
AU  - Julien Renaud
AU  - Ian W. Sutherland
AU  - Jeffrey C. Hertz
AU  - Jean-Marc Bonneville
AU  - Victor Arnaud
AU  - Camille Noûs
AU  - Bénédicte Fustec
AU  - Sébastien Boyer
AU  - Sébastien Marcombe
AU  - Jean-Philippe David
TI  - A genomic amplification affecting a carboxylesterase gene cluster confers organophosphate resistance in the mosquito <em>Aedes aegypti</em>: from genomic characterization to high-throughput field detection
AID  - 10.1101/2020.06.08.139741
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.06.08.139741
4099  - http://biorxiv.org/content/early/2020/11/04/2020.06.08.139741.short
4100  - http://biorxiv.org/content/early/2020/11/04/2020.06.08.139741.full
AB  - 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 characterise 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 ~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-colour 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.Competing Interest StatementThe authors have declared no competing interest.