Abstract

RNA interference (RNAi) is a naturally occurring process inhibiting gene expression, and recent advances in our understanding of the mechanism have allowed its development as a tool against insect pests. A major challenge for deployment in the field is the development of convenient and efficient methods for production of double stranded RNA (dsRNA). We assessed the potential for deploying bacterially produced dsRNA as a bio-pesticide against an invasive forest pest, the emerald ash borer (EAB). EAB feeds on the cambial tissue of ash trees (Fraxinus spp.), causing rapid death. EAB has killed millions of trees in North America since its discovery in 2002, prompting the need for innovative management strategies. In our study, bacterial expression and synthesis of dsRNA were performed with E. coli strain HT115 using the L4440 expression vector. EAB-specific dsRNAs (shi and hsp) over-expressed in E. coli were toxic to neonate EAB after oral administration, successfully triggering gene silencing and subsequent mortality; however, a non-specific dsRNA control was not included. Our results suggest that ingestion of transformed E. coli expressing dsRNAs can induce an RNAi response in EAB. To our knowledge, this is the first example of an effective RNAi response induced by feeding dsRNA-expressing bacteria in a forest pest.

Highlights

  • RNA interference (RNAi) regulates gene expression at the post-transcriptional level by degrading specific messenger RNAs, blocking translational efficiency [1]

  • In this study we evaluated the insecticidal potential of double stranded RNA (dsRNA)-expressing bacteria delivered orally to neonate emerald ash borer (EAB) larvae. dsRNA expressed in bacteria could provide dual benefits in terms of inexpensive production and efficient delivery

  • We showed that EAB fed with dsRNA-expressing bacteria results in downregulation of selected genes, demonstrating the potential for application of bacterially-expressed dsRNA for controlling

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Summary

Introduction

RNA interference (RNAi) regulates gene expression at the post-transcriptional level by degrading specific messenger RNAs (mRNA), blocking translational efficiency [1]. RNAi using exogenous dsRNA is emerging as a novel means of pest suppression [2]. DsRNA is recognized by the RNase III enzyme dicer and processed into small interfering RNAs (siRNAs). These siRNAs bind to the Argonaute protein and form an RNA-induced silencing complex (RISC), and the RISC complex binds to the complementary mRNA molecule, blocking gene expression [3]. While RNAi is emerging as an attractive option for insect pest control, convenient and efficient methods to produce and deliver dsRNA to target insects is challenging

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