Mutations in voltage-gated sodium channels from pyrethroid resistant salmon lice (Lepeophtheirus salmonis)

Pest Manag Sci. 2019 Feb;75(2):527-536. doi: 10.1002/ps.5151. Epub 2018 Sep 27.

Abstract

Background: Parasitic salmon lice (Lepeophtheirus salmonis) cause high economic losses in Atlantic salmon farming. Pyrethroids, which block arthropod voltage-gated sodium channels (Nav 1), are used for salmon delousing. However, pyrethroid resistance is common in L. salmonis. The present study characterized Nav 1 homologues in L. salmonis in order to identify channel mutations associated to resistance, called kdr (knockdown) mutations.

Results: Genome scans identified three L. salmonis Nav 1 homologues, LsNav 1.1, LsNav 1.2 and LsNav 1.3. Arthropod kdr mutations map to specific Nav 1 regions within domains DI-III, namely segments S5 and S6 and the linker helix connecting S4 and S5. The above channel regions were amplified by RT-PCR and sequenced in deltamethrin-susceptible and deltamethrin-resistant L. salmonis. While LsNav 1.1 and LsNav 1.2 lacked nucleotide polymorphisms showing association to resistance, LsNav 1.3 showed a non-synonymous mutation in S5 of DII occurring in deltamethrin-resistant parasites. The mutation is homologous to a previously described kdr mutation (I936V, numbering according to Musca domestica Vssc1) and was present in two pyrethroid-resistant L. salmonis strains (allele frequencies of 0.800 and 0.357), but absent in two pyrethroid-susceptible strains.

Conclusions: The present study indicates that a kdr-mutation in LsNaV 1.3 may contribute to deltamethrin resistance in L. salmonis. © 2018 Society of Chemical Industry.

Keywords: deltamethrin; resistance; sea lice; sodium channel.

MeSH terms

  • Animals
  • Copepoda / drug effects
  • Copepoda / genetics*
  • Insecticide Resistance / genetics*
  • Insecticides / pharmacology*
  • Mutation*
  • Nitriles / pharmacology*
  • Pyrethrins / pharmacology*
  • Salmo salar / parasitology
  • Sequence Analysis, Protein / veterinary
  • Voltage-Gated Sodium Channels / genetics*
  • Voltage-Gated Sodium Channels / metabolism

Substances

  • Insecticides
  • Nitriles
  • Pyrethrins
  • Voltage-Gated Sodium Channels
  • decamethrin