Aberrant splicing of a nicotinic acetylcholine receptor alpha 6 subunit is associated with spinosad tolerance in the thrips predator Orius laevigatus

Pestic Biochem Physiol. 2024 Mar:200:105837. doi: 10.1016/j.pestbp.2024.105837. Epub 2024 Feb 23.

Abstract

Susceptibility to insecticides is one of the limiting factors preventing wider adoption of natural enemies to control insect pest populations. Identification and selective breeding of insecticide tolerant strains of commercially used biological control agents (BCAs) is one of the approaches to overcome this constraint. Although a number of beneficial insects have been selected for increased tolerance to insecticides the molecular mechanisms underpinning these shifts in tolerance are not well characterised. Here we investigated the molecular mechanisms of enhanced tolerance of a lab selected strain of Orius laevigatus (Fieber) to the commonly used biopesticide spinosad. Transcriptomic analysis showed that spinosad tolerance is not a result of overexpressed detoxification genes. Molecular analysis of the target site for spinosyns, the nicotinic acetylcholine receptor (nAChR), revealed increased expression of truncated transcripts of the nAChR α6 subunit in the spinosad selected strain, a mechanism of resistance which was described previously in insect pest species. Collectively, our results demonstrate the mechanisms by which some beneficial biological control agents can evolve insecticide tolerance and will inform the development and deployment of insecticide-tolerant natural enemies in integrated pest management strategies.

Keywords: Beneficial insect; Biocontrol; Mechanism; Resistance; Spinosad.

MeSH terms

  • Animals
  • Biological Control Agents / pharmacology
  • Drug Combinations
  • Insecta / genetics
  • Insecticide Resistance / genetics
  • Insecticides* / toxicity
  • Macrolides / pharmacology
  • Receptors, Nicotinic* / genetics
  • Receptors, Nicotinic* / metabolism
  • Thysanoptera* / metabolism

Substances

  • Insecticides
  • spinosad
  • Biological Control Agents
  • Receptors, Nicotinic
  • Macrolides
  • Drug Combinations