CCHamide2-receptor regulates feeding behavior in the pea aphid, Acyrthosiphon pisum

Peptides. 2021 Sep:143:170596. doi: 10.1016/j.peptides.2021.170596. Epub 2021 Jun 9.

Abstract

Neuropeptide CCHamide-2 is a recently discovered peptide presents in many arthropods and it is the ligand of the CCHamide-2 receptor (CCHa2-R), which is playing a regulatory role in diverse physiological processes, such as feeding, insulin production, lipid metabolism, growth and reproduction, however, the function of this gene in aphids is still unknown. Here, we characterized and determined the presumed role of CCHa2-R signaling in the wingless pea aphid, Acyrthosiphon pisum. Quantitative real-time reverse transcription-PCR (qRT-PCR) revealed the expression levels of CCHa2-R transcripts in different development stages and different tissues, which indicates that the CCHa2-R expression was high in the first instar as compared to the upcoming nymphal instars and adult and was predominantly high in the brain. The CCHa2-R transcript levels were significantly up-regulated in starved aphids as compared to fed aphids. Moreover, RNAi knockdown by the injection of dsRNA-CCHa2-R significantly reduced the expression and also reduced their food intake in adult aphids, as revealed by electrical penetration graphs (EPGs) results. CCHa2-R-silencing was also shown to reduce reproduction but not survival in A. pisum. These observations suggest a role for the CCHa2-R pathway in the response of wingless parthenogenetic aphids to their nutritional status, and this role involves the regulation of the expression of CCHa2-R. Overall, the results of these experiments indicate that CCHa2-R plays a dominant role in the regulation of feeding in A. pisum.

Keywords: Acyrthosiphon pisum; CCHa2-R; CCHamide-2 receptor; Electrical penetration graphs; Feeding behavior; Neuropeptide; RNAi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aphids / metabolism*
  • Aphids / physiology
  • Feeding Behavior*
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Insect Proteins / metabolism
  • Insect Proteins / physiology
  • Neuropeptides / metabolism
  • RNA Interference
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, G-Protein-Coupled / physiology
  • Signal Transduction

Substances

  • Insect Proteins
  • Neuropeptides
  • Receptors, G-Protein-Coupled