Characterization of two Bursicon genes and their association with wing development in the brown citrus aphid, Aphis citricidus

Insect Sci. 2024 Dec;31(6):1684-1696. doi: 10.1111/1744-7917.13337. Epub 2024 Feb 9.

Abstract

The tanning hormone, Bursicon, is a neuropeptide secreted by the insect nervous system that functions as a heterodimer composed of Burs-α and Burs-β subunits. It plays a critical role in the processes of cuticle tanning and wing expansion in insects. In this study, we successfully identified the AcBurs-α and AcBurs-β genes in Aphis citricidus. The open reading frames of AcBurs-α and AcBurs-β were 480 and 417 bp in length, respectively. Both AcBurs-α and AcBurs-β exhibited 11 conserved cysteine residues. AcBurs-α and AcBurs-β were expressed during all developmental stages of A. citricidus and showed high expression levels in the winged aphids. To investigate the potential role of AcBurs-α and AcBurs-β in wing development, we employed RNA interference (RNAi) techniques. With the efficient silencing of AcBurs-α (44.90%) and AcBurs-β (52.31%), malformed wings were induced in aphids. The proportions of malformed wings were 22.50%, 25.84%, and 38.34% in dsAcBurs-α-, dsAcBur-β-, and dsAcBurs-α + dsAcBur-β-treated groups, respectively. Moreover, feeding protein kinase A inhibitors (H-89) also increased the proportion of malformed wings to 30.00%. Feeding both double-stranded RNA and inhibitors (H-89) significantly downregulated the wing development-related genes nubbin, vestigial, notch and spalt major. Silence of vestigial through RNAi also led to malformed wings. Meanwhile, the exogenous application of 3 hormones that influence wing development did not affect the expression level of AcBursicon genes. These findings indicate that AcBursicon genes plays a crucial role in wing development in A. citricidus; therefore, it represents a potential molecular target for the control of this pest through RNAi-based approaches.

Keywords: Aphis citricidus; Bursicon; PKA; RNA interference; transcriptome; wing development.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aphids* / genetics
  • Aphids* / growth & development
  • Insect Proteins* / genetics
  • Insect Proteins* / metabolism
  • Invertebrate Hormones / genetics
  • Invertebrate Hormones / metabolism
  • Phylogeny
  • RNA Interference
  • Wings, Animal* / growth & development

Substances

  • bursicon
  • Insect Proteins
  • Invertebrate Hormones