Smidler Andrea L, Apte Reema A, Pai James J, Chow Martha L, Chen Sanle, Mondal Agastya, Sánchez C Héctor M, Antoshechkin Igor, Marshall John M, Akbari Omar S
School of Biological Sciences, Department of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA 92093.
Divisions of Epidemiology & Biostatistics, School of Public Health, University of California, Berkeley, CA 94720, USA.
bioRxiv. 2023 Jul 21:2023.07.20.549947. doi: 10.1101/2023.07.20.549947.
Controlling the principal African malaria vector, the mosquito , is considered essential to curtail malaria transmission. However existing vector control technologies rely on insecticides, which are becoming increasingly ineffective. Sterile insect technique (SIT) is a powerful suppression approach that has successfully eradicated a number of insect pests, yet the toolkit lacks the requisite technologies for its implementation. SIT relies on iterative mass-releases of non-biting, non-driving, sterile males which seek out and mate with monandrous wild females. Once mated, females are permanently sterilized due to mating-induced refractoriness, which results in population suppression of the subsequent generation. However, sterilization by traditional methods renders males unfit, making the creation of precise genetic sterilization methods imperative. Here we develop precision guided Sterile Insect Technique (pgSIT) in the mosquito for inducible, programmed male-sterilization and female-elimination for wide scale use in SIT campaigns. Using a binary CRISPR strategy, we cross separate engineered Cas9 and gRNA strains to disrupt male-fertility and female-essential genes, yielding >99.5% male-sterility and >99.9% female-lethality in hybrid progeny. We demonstrate that these genetically sterilized males have good longevity, are able to induce population suppression in cage trials, and are predicted to eliminate wild populations using mathematical models, making them ideal candidates for release. This work provides a valuable addition to the malaria genetic biocontrol toolkit, for the first time enabling scalable SIT-like confinable suppression in the species.
控制非洲主要疟疾传播媒介蚊子被认为是减少疟疾传播的关键。然而,现有的病媒控制技术依赖杀虫剂,而杀虫剂的效果正变得越来越差。昆虫不育技术(SIT)是一种有效的抑制方法,已成功根除了多种害虫,但该技术缺乏实施所需的必要技术。SIT依赖于反复大量释放不叮咬、不驱避的不育雄蚊,这些雄蚊会寻找单配的野生雌蚊并与之交配。一旦交配,雌蚊会因交配诱导的不应性而永久绝育,从而导致下一代种群数量受到抑制。然而,传统方法进行的绝育会使雄蚊失去生殖能力,因此开发精确的基因绝育方法势在必行。在此,我们开发了蚊子精确制导昆虫不育技术(pgSIT),用于诱导性、程序性雄性绝育和雌性消除,以便在SIT防治活动中广泛应用。利用二元CRISPR策略,我们将分别经过基因工程改造的Cas9和gRNA品系杂交,以破坏雄性生育力和雌性必需基因,在杂交后代中产生了>99.5%的雄性不育率和>99.9%的雌性致死率。我们证明,这些基因绝育的雄蚊寿命长,能够在笼养试验中诱导种群数量减少,并且通过数学模型预测能够消灭野生种群,使其成为理想的释放候选对象。这项工作为疟疾遗传生物防治工具包增添了宝贵内容,首次实现了在该物种中类似SIT的可扩展、可限制的抑制效果。