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Updated: May 10, 2025

Larval RNA Interference in the Red Flour Beetle, Tribolium castaneum
Published on: October 13, 2014
RNAi effect in target and non-target pests correlates with the length of continuous matches in dsRNA sequences
Zhaoyang Li1, Junna Liu1, Satyabrata Nanda2
1State Key Laboratory of Green Pesticide, Engineering Research Center of Biocontrol, Ministry of Education, South China Agricultural University, Guangzhou 510642, China.
Abstract:
RNA interference (RNAi) has emerged as a promising and environmentally friendly approach for controlling the pest Henosepilachna vigintioctopunctata (Hvig). Identifying lethal target genes in Hvig and evaluating the efficacy of oral dsRNA administration are crucial steps in this process. Additionally, assessing the potential risks of RNAi to non-target organisms (NTOs) is essential to ensure environmental safety. A soluble N-ethylmaleimide-sensitive factor attachment protein α (αSNAP) is an essential component of membrane fusion machinery, offering as a potential target gene for RNAi-based pest control. This study found that silencing of Hvαsnap with varying dsRNA concentrations (6.25, 12.5, 25, 50, 100, 200 ng/μL) induced 53.33 %-100 % lethality in Hvig, with an LC50 value of 10.15 ng/μL. Feeding the NTO, Propylaea japonica with dsHvαsnap or dsPjαsnap-1 containing 3-21-nt consecutive matches had no notable effects on survival, development, pupal weight, or gene expression. However, injecting these dsRNAs significantly increased P. japonica mortality. A chimeric dsGFP-αsnap-17-nt suppressed Hvαsnap expression and reduced Hvig larval survival but failed to induce RNAi in P. japonica. Overall, this study suggests that different species exhibit varying sensitivities to dsRNA, and increasing the number of consecutive matching bases may enhance RNAi effects in NTOs.
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