PT - JOURNAL ARTICLE AU - Ming Li AU - Ting Yang AU - Nikolay P. Kandul AU - Michelle Bui AU - Stephanie Gamez AU - Robyn Raban AU - Jared Bennett AU - Héctor M. Sánchez C. AU - Gregory C. Lanzaro AU - Hanno Schmidt AU - Yoosook Lee AU - John M. Marshall AU - Omar S. Akbari TI - Development of a Confinable Gene-Drive System in the Human Disease Vector, <em>Aedes aegypti</em> AID - 10.1101/645440 DP - 2019 Jan 01 TA - bioRxiv PG - 645440 4099 - http://biorxiv.org/content/early/2019/05/24/645440.short 4100 - http://biorxiv.org/content/early/2019/05/24/645440.full AB - Aedes aegypti, the principal mosquito vector for many arboviruses that causes yellow fever, dengue, Zika, and chikungunya, increasingly infects millions of people every year. With an escalating burden of infections and the relative failure of traditional control methods, the development of innovative control measures has become of paramount importance. The use of gene drives has recently sparked significant enthusiasm for the genetic control of mosquito populations, however no such system has been developed in Ae. aegypti. To fill this void and demonstrate efficacy in Ae. aegypti, here we develop several CRISPR-based split-gene drives for use in this vector. With cleavage rates up to 100% and transmission rates as high as 94%, mathematical models predict that these systems could spread anti-pathogen effector genes into wild Ae. aegypti populations in a safe, confinable and reversible manner appropriate for field trials and effective for controlling disease. These findings could expedite the development of effector-linked gene drives that could safely control wild populations of Ae. aegypti to combat local pathogen transmission.Significance Statement Ae. aegypti is a globally distributed arbovirus vector spreading deadly pathogens to millions of people annually. Current control methods are inadequate and therefore new technologies need to be innovated and implemented. With the aim of providing new tools for controlling this pest, here we engineered and tested several split gene drives in this species. These drives functioned at very high efficiency and may provide a tool to fill the void in controlling this vector. Taken together, our results provide compelling path forward for the feasibility of future effector-linked split-drive technologies that can contribute to the safe, sustained control and potentially the elimination of pathogens transmitted by this species.