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Engineered resistance to Zika virus in transgenic Aedes aegypti expressing a polycistronic cluster of synthetic small RNAs

Proc Natl Acad Sci U S A. 2019; 
Buchman A, Gamez S, Li M, Antoshechkin I, Li HH, Wang HW, Chen CH, Klein MJ, Duchemin JB, Paradkar PN, Akbari OS,
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Gene Synthesis To generate vector OA959C (the anti-ZIKV transgene), several components were cloned into the piggyBac plasmid pBac[3xP3-DsRed] [6] using Gibson assembly/EA cloning [7]. First, a Drosophila codon optimized tdTomato marker was amplified with primers 959C.10A and 959C.10B from a gene synthesized vector (GenScript, Piscataway, NJ) and cloned into a XhoI/FseI digested pBac[3xP3-DsRed] backbone using EA cloning. Get A Quote

摘要

Recent Zika virus (ZIKV) outbreaks have highlighted the necessity for development of novel vector control strategies to combat arboviral transmission, including genetic versions of the sterile insect technique, artificial infection with Wolbachia to reduce population size and/or vectoring competency, and gene drive-based methods. Here, we describe the development of mosquitoes synthetically engineered to impede vector competence to ZIKV. We demonstrate that a polycistronic cluster of engineered synthetic small RNAs targeting ZIKV is expressed and fully processed in Aedes aegypti, ensuring the formation of mature synthetic small RNAs in the midgut where ZIKV resides in the early stages of infection. Critically, ... More

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