Link to bioRxiv paper:

http://biorxiv.org/cgi/content/short/2020.08.02.233056v1?rss=1

Authors: Adolfi, A., Gantz, V. M., Jasinskiene, N., Lee, H.-F., Hwang, K., Bulger, E. A., Ramaiah, A., Bennett, J. B., Terradas, G., Emerson, J. J., Marshall, J. M., Bier, E., James, A. A.

Abstract:

The development of Cas9/gRNA-mediated gene-drive systems has bolstered the advancement of genetic technologies for controlling vector-borne pathogen transmission. These include population suppression approaches, genetic analogs of insecticidal techniques that reduce the number of vector insects, and population modification (replacement/alteration) approaches, which interfere with competence to transmit pathogens. We developed the first recoded gene-drive rescue system for population modification in the malaria vector, Anopheles stephensi, that relieves the load in females caused by integration of the drive into the kynurenine hydroxylase gene by rescuing its function. Non-functional resistant alleles are eliminated via a dominantly-acting maternal effect combined with slower-acting standard negative selection, and a functional resistant allele does not prevent drive invasion. Small cage trials show that single releases of gene-drive males robustly result in efficient population modification with >95% of mosquitoes carrying the drive within 5-11 generations over a range of initial release ratios.

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