Project Number: 6615-22000-025-20
Start Date: Dec 09, 2013
End Date: Aug 31, 2015
Methodology for transposon-mediated germ-line transformation of Diaphorina citri will be developed and transgenic strains of the plant disease vector will be created for either population replacement or suppression. Transposon vectors to be tested will include the piggyBac and Minos transposable elements marked with polyubiquitin-regulated fluorescent proteins. Protocols will initially include embryonic microinjection of vector and helper plasmids, that will be extended to maternal abdominal injection, electroporation and biolistics delivery. Efficient transformation protocols will then be used to create vector-incompetent transgenic ACP having a synthetic “Medea-like” element that will replace vector-competent strains in the field. Transgenic strains will also be created having a conditional tetracycline-suppressible embryonic lethality system that will result in inviable progeny after field release.