Sensillar expression and responses of olfactory receptors reveal different peripheral coding in two Helicoverpa species using the same pheromone components

Sci Rep. 2016 Jan 8:6:18742. doi: 10.1038/srep18742.

Abstract

Male moths efficiently recognize conspecific sex pheromones thanks to their highly accurate and specific olfactory system. The Heliothis/Helicoverpa species are regarded as good models for studying the perception of sex pheromones. In this study, we performed a series of experiments to investigate the peripheral mechanisms of pheromone coding in two-closely related species, Helicoverpa armigera and H. assulta. The morphology and distribution patterns of sensilla trichoidea are similar between the two species when observed at the scanning electron microscope, but their performances are different. In H. armigera, three functional types of sensilla trichoidea (A, B and C) were found to respond to different pheromone components, while in H. assulta only two types of such sensilla (A and C) could be detected. The response profiles of all types of sensilla trichoidea in the two species well matched the specificities of the pheromone receptors (PRs) expressed in the same sensilla, as measured in voltage-clamp experiments. The expressions of PRs in neighboring olfactory sensory neurons (OSNs) within the same trichoid sensillum were further confirmed by in situ hybridization. Our results show how the same pheromone components can code for different messages at the periphery of two Helicoverpa species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Female
  • Gene Expression Regulation
  • In Situ Hybridization, Fluorescence
  • Male
  • Microscopy, Electron, Scanning
  • Moths / physiology*
  • Moths / ultrastructure
  • Olfactory Perception / physiology*
  • Olfactory Receptor Neurons / physiology*
  • Olfactory Receptor Neurons / ultrastructure
  • Patch-Clamp Techniques
  • Receptors, Pheromone / genetics
  • Receptors, Pheromone / metabolism*
  • Sensilla / physiology*
  • Sensilla / ultrastructure
  • Sex Attractants / genetics
  • Sex Attractants / metabolism*
  • Signal Transduction
  • Species Specificity

Substances

  • Receptors, Pheromone
  • Sex Attractants