Sex peptide receptor is not required for refractoriness to remating or induction of egg laying in Aedes aegypti

Genetics. 2024 May 7;227(1):iyae034. doi: 10.1093/genetics/iyae034.

Abstract

Across diverse insect taxa, the behavior and physiology of females dramatically changes after mating-processes largely triggered by the transfer of seminal proteins from their mates. In the vinegar fly Drosophila melanogaster, the seminal protein sex peptide (SP) decreases the likelihood of female flies remating and causes additional behavioral and physiological changes that promote fertility including increasing egg production. Although SP is only found in the Drosophila genus, its receptor, sex peptide receptor (SPR), is the widely conserved myoinhibitory peptide (MIP) receptor. To test the functional role of SPR in mediating postmating responses in a non-Drosophila dipteran, we generated 2 independent Spr-knockout alleles in the yellow fever mosquito, Aedes aegypti. Although SPR is needed for postmating responses in Drosophila and the cotton bollworm Helicoverpa armigera, Spr mutant Ae. aegypti show completely normal postmating decreases in remating propensity and increases in egg laying. In addition, injection of synthetic SP or accessory gland homogenate from D. melanogaster into virgin female mosquitoes did not elicit these postmating responses. Our results demonstrate that Spr is not required for these canonical postmating responses in Ae. aegypti, indicating that other, as yet unknown, signaling pathways are likely responsible for these behavioral switches in this disease vector.

Keywords: Aedes aegypti; mating receptivity; oviposition; reproduction; sex peptide.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aedes* / genetics
  • Aedes* / physiology
  • Animals
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / physiology
  • Female
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Male
  • Oviposition*
  • Receptors, Invertebrate Peptide / genetics
  • Receptors, Invertebrate Peptide / metabolism
  • Receptors, Peptide / genetics
  • Receptors, Peptide / metabolism
  • Sexual Behavior, Animal

Substances

  • Drosophila Proteins
  • Receptors, Invertebrate Peptide
  • sex peptide receptor, Drosophila
  • Insect Proteins
  • Receptors, Peptide