Knockdown of RNA interference pathway genes impacts the fitness of western corn rootworm

Sci Rep. 2018 May 18;8(1):7858. doi: 10.1038/s41598-018-26129-6.

Abstract

Western corn rootworm (Diabrotica virgifera virgifera) is a serious agricultural pest known for its high adaptability to various management strategies, giving rise to a continual need for new control options. Transgenic maize expressing insecticidal RNAs represents a novel mode of action for rootworm management that is dependent on the RNA interference (RNAi) pathways of the insect for efficacy. Preliminary evidence suggests that western corn rootworm could develop broad resistance to all insecticidal RNAs through changes in RNAi pathway genes; however, the likelihood of field-evolved resistance occurring through this mechanism remains unclear. In the current study, eight key genes involved in facilitating interference in the microRNA and small interfering RNA pathways were targeted for knockdown in order to evaluate impact on fitness of western corn rootworm. These genes include drosha, dicer-1, dicer-2, pasha, loquacious, r2d2, argonaute 1, and argonaute 2. Depletion of targeted transcripts in rootworm larvae led to changes in microRNA expression, decreased ability to pupate, reduced adult beetle emergence, and diminished reproductive capacity. The observed effects do not support evolution of resistance through changes in expression of these eight genes due to reduced insect fitness.

MeSH terms

  • Animals
  • Coleoptera / growth & development
  • Coleoptera / physiology
  • Gene Expression Regulation
  • Insect Proteins / antagonists & inhibitors
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Larva / growth & development
  • Larva / metabolism
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Plant Roots / genetics
  • Plant Roots / metabolism
  • Plant Roots / parasitology
  • Plants, Genetically Modified / genetics
  • Plants, Genetically Modified / metabolism
  • Plants, Genetically Modified / parasitology
  • RNA Interference*
  • RNA, Double-Stranded / genetics*
  • RNA, Double-Stranded / metabolism
  • RNA, Small Interfering / antagonists & inhibitors
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Ribonuclease III / antagonists & inhibitors
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism
  • Zea mays / genetics*
  • Zea mays / metabolism
  • Zea mays / parasitology

Substances

  • Insect Proteins
  • MicroRNAs
  • RNA, Double-Stranded
  • RNA, Small Interfering
  • Ribonuclease III