Cattel Julien, Haberkorn Chloé, Laporte Fréderic, Gaude Thierry, Cumer Tristan, Renaud Julien, Sutherland Ian W, Hertz Jeffrey C, Bonneville Jean-Marc, Arnaud Victor, Fustec Bénédicte, Boyer Sébastien, Marcombe Sébastien, David Jean-Philippe
Laboratoire d'Ecologie Alpine (LECA) UMR 5553 CNRS - Université Grenoble-Alpes Grenoble France.
Present address: Symbiosis Technologies for Insect Control (SymbioTIC) Plateforme de Recherche Cyroi Ste Clotilde France.
Evol Appl. 2021 Feb 16;14(4):1009-1022. doi: 10.1111/eva.13177. eCollection 2021 Apr.
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 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-color multiplex TaqMan assay allowing the rapid detection and copy number quantification of this amplification event in 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.
通过改变基因表达和产生旁系同源基因,基因组扩增是短期适应性过程的关键组成部分。在昆虫中,使用杀虫剂可选择导致解毒酶表达增加的基因扩增,这支持了这些DNA标记物在监测田间抗性等位基因动态方面的实用性。在此背景下,本研究旨在表征与蚊子对有机磷杀虫剂抗性相关的基因组扩增事件,并开发一种分子检测方法以监测田间相关的抗性等位基因。一项使用来自老挝的复合种群进行的实验进化实验支持了2号染色体上多个相邻羧酸酯酶基因的过度转录与对多种有机磷杀虫剂抗性之间的关联。结合全基因组测序和特定基因的定量PCR,证实了该位点存在一个跨越至少五个羧酸酯酶基因的约100 kb扩增,且存在多种结构重复单倍型。田间数据证实了它们在东南亚的传播,并揭示了种群间和种群内的高拷贝数多态性,这表明这种抗性机制与相关的适合度代价之间存在权衡。开发了一种双色多重TaqMan检测方法,可在田间种群中快速检测和定量该扩增事件的拷贝数,并进行了验证。这种新型检测方法的常规使用将改善对这种主要虫媒病毒载体中抗性等位基因的追踪。