Acetylcholine esterase of Drosophila melanogaster: a laboratory model to explore applications of insecticide susceptibility gene drives

Natalia Hernandes, Mollyann Xiaomeng Qi, Soumitra Bhide, Courtney Brown, Benjamin J Camm, Simon W Baxter, Charles Robin
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Abstract

BACKGROUND: One of the proposed applications of gene drives has been to revert pesticide resistant mutations back to the ancestral susceptible state. Insecticides that have become ineffective because of the rise of resistance could have reinvigorated utility and be used to suppress pest populations again, perhaps at lower application doses. RESULTS: We have created a laboratory model for susceptibility gene drives that replaces field-selected resistant variants of the acetylcholine esterase (Ace) locus of Drosophila melanogaster with ancestral susceptible variants. We constructed a CRISPR/Cas9 homing drive and found that homing occurred in many genetic backgrounds with varying efficiencies. While the drive itself could not be homozygosed, it converted resistant alleles into susceptible ones and produced recessive lethal alleles that could suppress populations. Our studies provided evidence for two distinct classes of Gene Drive Resistance (GDR): rather than being mediated by the conventional Non-Homologous End-joining (NHEJ) pathway, one seemed to involve short homologous repair and the other was defined by genetic background. Additionally, we used simulations to explore a distinct application of susceptibility drives; the use of chemicals to prevent the spread of synthetic gene drives into protected areas. CONCLUSIONS: Insecticide susceptibility gene drives could be useful tools to control pest insects however problems associated with particularities of the target loci and GDR will need to be overcome for them to be effective. Furthermore, realistic patterns of pest dispersal and high insecticide exposure rates would be required if susceptibility were to be useful as safety-switch to prevent the unwanted spread of gene drives.
黑腹果蝇乙酰胆碱酯酶:一个探索杀虫剂敏感性基因驱动应用的实验室模型
背景:基因驱动的应用之一是将农药抗性突变恢复到祖先的易感状态。由于抗药性上升而变得无效的杀虫剂本可以重新发挥效用,并再次用于抑制害虫种群,也许使用剂量较低。结果:我们建立了一个易感基因驱动的实验室模型,用祖先的易感变异取代黑腹果蝇乙酰胆碱酯酶(Ace)位点的田间选择抗性变异。我们构建了CRISPR/Cas9归巢驱动,发现归巢发生在许多遗传背景中,效率各不相同。虽然驱动本身不能纯合,但它将抗性等位基因转化为易感等位基因,并产生可以抑制种群的隐性致死等位基因。我们的研究为两种不同类型的基因驱动抗性(GDR)提供了证据:一种似乎涉及短同源修复,而不是由传统的非同源末端连接(NHEJ)途径介导,另一种则由遗传背景定义。此外,我们使用模拟来探索磁化率驱动的独特应用;使用化学物质防止合成基因驱动扩散到保护区。结论:杀虫剂易感基因驱动可能是控制害虫的有用工具,但需要克服与目标基因座和GDR的特殊性相关的问题才能有效。此外,如果要使易感性成为防止基因驱动的不必要传播的安全开关,就需要害虫扩散的现实模式和较高的杀虫剂暴露率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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