Abstract
The bacterial endosymbiont Wolbachia has emerged as an effective biocontrol method to reduce arbovirus transmission. Transinfection of wMel Wolbachia from Drosophila melanogaster to Aedes aegypti results in the transfer of important Wolbachia-induced phenotypes including the reproductive modification, cytoplasmic incompatibility, and inhibition of viruses including dengue and chikungunya. However, the mechanisms underlying these critical traits as well other Wolbachia-host interactions are still not fully understood. Recently an in vitro genome wide RNAi screen was performed on wMel-infected Drosophila S2 cells and identified large cohorts of host genes that alter wMel density when targeted. If these findings can be replicated in vivo, this would provide a powerful tool for modulating wMel density both systemically and in a tissue-specific manner allowing for interrogation of wMel-host interactions. Here, we used the GAL4/UAS system to express RNAi molecules targeting host gene candidates previously identified to dysregulate wMel density in vitro. We found systemic knockdown of two candidate D. melanogaster genes does not lead to wMel density dysregulation. To explore the lack of consistency between our study and previous work, we also examined native tissue-specific density of wMel in D. melanogaster. We show density is varied between tissues and find that individual tissue densities are not reliable linear predictors of other tissue densities. Our results demonstrate the complexities of implementing in vitro findings in systemic applications.
