PLoS ONE (Jan 2017)

Nucleases as a barrier to gene silencing in the cotton boll weevil, Anthonomus grandis.

  • Rayssa Almeida Garcia,
  • Leonardo Lima Pepino Macedo,
  • Danila Cabral do Nascimento,
  • François-Xavier Gillet,
  • Clidia Eduarda Moreira-Pinto,
  • Muhammad Faheem,
  • Angelina Maria Moreschi Basso,
  • Maria Cristina Mattar Silva,
  • Maria Fatima Grossi-de-Sa

DOI
https://doi.org/10.1371/journal.pone.0189600
Journal volume & issue
Vol. 12, no. 12
p. e0189600

Abstract

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RNA interference (RNAi) approaches have been applied as a biotechnological tool for controlling plant insect pests via selective gene down regulation. However, the inefficiency of RNAi mechanism in insects is associated with several barriers, including dsRNA delivery and uptake by the cell, dsRNA interaction with the cellular membrane receptor and dsRNA exposure to insect gut nucleases during feeding. The cotton boll weevil (Anthonomus grandis) is a coleopteran in which RNAi-mediated gene silencing does not function efficiently through dsRNA feeding, and the factors involved in the mechanism remain unknown. Herein, we identified three nucleases in the cotton boll weevil transcriptome denoted AgraNuc1, AgraNuc2, and AgraNuc3, and the influences of these nucleases on the gene silencing of A. grandis chitin synthase II (AgraChSII) were evaluated through oral dsRNA feeding trials. A phylogenetic analysis showed that all three nucleases share high similarity with the DNA/RNA non-specific endonuclease family of other insects. These nucleases were found to be mainly expressed in the posterior midgut region of the insect. Two days after nuclease RNAi-mediated gene silencing, dsRNA degradation by the gut juice was substantially reduced. Notably, after nucleases gene silencing, the orally delivered dsRNA against the AgraChSII gene resulted in improved gene silencing efficiency when compared to the control (non-silenced nucleases). The data presented here demonstrates that A. grandis midgut nucleases are effectively one of the main barriers to dsRNA delivery and emphasize the need to develop novel RNAi delivery strategies focusing on protecting the dsRNA from gut nucleases and enhancing its oral delivery and uptake to crop insect pests.