Cattel Julien, Faucon Frédéric, Le Péron Bastien, Sherpa Stéphanie, Monchal Marie, Grillet Lucie, Gaude Thierry, Laporte Frederic, Dusfour Isabelle, Reynaud Stéphane, David Jean-Philippe
Laboratoire d'Ecologie Alpine (LECA) UMR 5553 CNRS - Université Grenoble-Alpes Grenoble France.
Institut Pasteur de la Guyane Cayenne France.
Evol Appl. 2019 Sep 27;13(2):303-317. doi: 10.1111/eva.12867. eCollection 2020 Feb.
In addition to combating vector-borne diseases, studying the adaptation of mosquitoes to insecticides provides a remarkable example of evolution-in-action driving the selection of complex phenotypes. Actually, most resistant mosquito populations show multi-resistance phenotypes as a consequence of the variety of insecticides employed and of the complexity of selected resistance mechanisms. Such complexity makes the identification of alleles conferring resistance to specific insecticides challenging and prevents the development of molecular assays to track them in the field. Here we showed that combining simple genetic crosses with pool targeted DNA-seq can enhance the specificity of resistance allele's detection while maintaining experimental work and sequencing effort at reasonable levels. A multi-resistant population of the mosquito was exposed to three distinct insecticides (deltamethrin, bendiocarb and fenitrothion), and survivors to each insecticide were crossed with a susceptible strain to generate three distinct lines. F2 individuals from each line were then segregated based on their survival to two insecticide doses. Hundreds of genes covering all detoxifying enzymes and insecticide targets together with more than 7,000 intergenic regions equally spread over mosquito genome were sequenced from pools of F0 and F2 individuals unexposed or surviving insecticide. Differential coverage analysis identified 39 detoxification enzymes showing an increased gene copy number in association with resistance. Combining an allele frequency filtering approach with a Bayesian -based genome scan identified multiple genomic regions showing strong selection signatures together with 50 nonsynonymous variations associated with resistance. This study provides a simple and cost-effective approach to improve the specificity of resistance allele's detection in multi-resistant populations while reducing false positives frequently arising when comparing populations showing divergent genetic backgrounds. The identification of novel DNA resistance markers opens new opportunities for improving the tracking of insecticide resistance in the field.
除了抗击媒介传播疾病外,研究蚊子对杀虫剂的适应性还提供了一个显著的实例,展示了实际发生的进化如何推动复杂表型的选择。事实上,由于所使用杀虫剂的种类以及所选抗性机制的复杂性,大多数抗性蚊子种群表现出多抗性表型。这种复杂性使得鉴定赋予对特定杀虫剂抗性的等位基因具有挑战性,并阻碍了在野外追踪这些等位基因的分子检测方法的开发。在这里,我们表明,将简单的遗传杂交与混合靶向DNA测序相结合,可以提高抗性等位基因检测的特异性,同时将实验工作和测序工作量维持在合理水平。将一个多抗性蚊子种群暴露于三种不同的杀虫剂(溴氰菊酯、残杀威和杀螟硫磷),每种杀虫剂的存活者与一个敏感品系杂交,以产生三个不同的品系。然后根据每个品系的F2个体对两种杀虫剂剂量的存活情况进行分离。从未接触或在杀虫剂处理后存活的F0和F2个体池中,对涵盖所有解毒酶和杀虫剂靶标的数百个基因以及均匀分布在蚊子基因组上的7000多个基因间区域进行了测序。差异覆盖分析确定了39种解毒酶,其基因拷贝数增加与抗性相关。将等位基因频率过滤方法与基于贝叶斯的基因组扫描相结合,鉴定出多个显示出强烈选择特征的基因组区域以及50个与抗性相关的非同义变异。这项研究提供了一种简单且经济高效的方法,可提高多抗性种群中抗性等位基因检测的特异性,同时减少在比较具有不同遗传背景的种群时经常出现的假阳性。新型DNA抗性标记的鉴定为改进野外杀虫剂抗性的追踪开辟了新机会。