The Brugia malayi neuropeptide receptor-4 is activated by FMRFamide-like peptides and signals via Gαi

Mol Biochem Parasitol. 2014 Jun;195(1):54-8. doi: 10.1016/j.molbiopara.2014.07.002. Epub 2014 Jul 16.

Abstract

Genetic studies undertaken in the model organism Caenorhabditis elegans have demonstrated the importance of neuropeptidergic signalling in nematode physiology. Disruption of this signalling may have deleterious phenotypic consequences, including altered locomotion, feeding behaviour, and reproduction. Neuropeptide G protein-coupled receptors (GPCRs) that transduce many of these signals therefore represent cogent drug targets. Recently published genomic sequencing data for a number of parasitic helminths of medical and veterinary importance has revealed the apparent conservation of a number of neuropeptides, and neuropeptide receptors between parasitic and free-living species, raising the intriguing possibility of developing broad-spectrum anthelmintic therapeutics. Here, we identify and clone a neuropeptide receptor, NPR-4, from the human filarial nematode Brugia malayi and demonstrate its activation in vitro, by FMRFamide-like peptides of the FLP-18 family, and intracellular signalling via Gαi mediated pathways. These data represent the first example of deorphanisation of a neuropeptide GPCR in any parasitic helminth species.

Keywords: Brugia malayi; FMRFamide-like peptides; G protein-coupled receptor; Lymphatic filariasis; Neuropeptide; Neuropeptide receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brugia malayi / chemistry
  • Brugia malayi / genetics
  • Brugia malayi / metabolism*
  • Caenorhabditis elegans
  • Filariasis / metabolism*
  • Filariasis / parasitology*
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism*
  • Helminth Proteins / genetics
  • Helminth Proteins / metabolism*
  • Humans
  • Molecular Sequence Data
  • Neuropeptides / chemistry
  • Neuropeptides / genetics
  • Neuropeptides / metabolism*
  • Receptors, Neuropeptide / genetics
  • Receptors, Neuropeptide / metabolism*
  • Sequence Alignment
  • Signal Transduction

Substances

  • Helminth Proteins
  • Neuropeptides
  • Receptors, Neuropeptide
  • GTP-Binding Protein alpha Subunits, Gi-Go