A glycine residue essential for high ivermectin sensitivity in Cys-loop ion channel receptors

Int J Parasitol. 2010 Nov;40(13):1477-81. doi: 10.1016/j.ijpara.2010.07.010. Epub 2010 Aug 14.

Abstract

Ivermectin exerts its anthelmintic effect by activating nematode Cys-loop glutamate-gated receptors. Here we show that a glycine residue at a specific transmembrane domain location is essential for high ivermectin sensitivity in both glycine- and glutamate-gated Cys-loop receptors. We also show that ivermectin sensitivity can be conferred on an ivermectin-insensitive receptor by introducing a glycine at this position. Furthermore, comparison of amino acid sequences of ivermectin-sensitive and -resistant receptors reveals that the presence of a glycine reliably predicts ivermectin sensitivity. By providing a means of identifying ivermectin-sensitive receptors, this finding should help in characterising ivermectin-resistance mechanisms and identifying new anthelmintic targets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution / genetics
  • Animals
  • Anthelmintics / metabolism*
  • Anthelmintics / pharmacology
  • Cysteine Loop Ligand-Gated Ion Channel Receptors / genetics*
  • Cysteine Loop Ligand-Gated Ion Channel Receptors / metabolism*
  • Drug Resistance
  • Glycine / genetics*
  • Ivermectin / metabolism*
  • Ivermectin / pharmacology
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nematoda / drug effects*
  • Protein Structure, Quaternary
  • Sequence Alignment

Substances

  • Anthelmintics
  • Cysteine Loop Ligand-Gated Ion Channel Receptors
  • Ivermectin
  • Glycine