Tony Nolan of Imperial College London, U.K., and colleagues designed a gene drive that targeted genes involved in egg production to successfully reduce the number of offspring that female Anopheles gambiae mosquitoes produced. The drive included a CRISPR-Cas9–based system to copy the fertility-reducing elements onto homologous chromosomes, so that the gene drive was inherited by nearly all offspring, rather than just half—resulting in its spread through the entire captive population within just four generations. But the insects soon began to evolve mutations that restored fertility and blocked the continued spread of the gene drive.
“Reducing the numbers of mosquito vectors has been the most effective tool to date for the control of malaria, so self-sustaining gene drives designed with this purpose have great potential,” Nolan says in a press release. “However gene drives are not a silver bullet and just like antibiotics can select for resistance in bacteria, gene drives can be susceptible to resistance at their target site.”
See “Using Gene Drives to Limit the Spread of Malaria” (written by Nolan and colleague)
Documenting mutations that convey resistance to a gene drive, as this study does, could inform the future development of more-robust technologies, the researchers say. “Our findings allow us to improve predictions on gene drive behaviour and to make concrete recommendations on how to improve future gene drive designs by decreasing the likelihood that they generate resistance,” they write in their paper.