Molecular characterisation of a sodium channel gene and identification of a Phe1538 to Ile mutation in citrus red mite, Panonychus citri

Pest Manag Sci. 2015 Feb;71(2):266-77. doi: 10.1002/ps.3802. Epub 2014 May 15.

Abstract

Background: The citrus red mite, Panonychus citri (McGregor), is regarded as one of the most serious citrus pests in many countries and has developed high resistance to pyrethroids as a result of the intensive use of these acaricides.

Results: The para sodium channel gene of P. citri (named PcNav ), containing an entire coding region of 6729 bp, was cloned in this study. Three alternative splicing sites and 12 potential RNA editing sites were identified in PcNav . Thus, exons alt 1 and alt 3-v3 were found to be unique to PcNav . Comparison of field fenpropathrin-resistant (WZ) and susceptible (LS) strains identified the point mutation F1538I in IIIS6 of the sodium channel, which is known to confer strong resistance to pyrethroids in mites. Moreover, it was also found that the PcNav mRNA was present during all life stages, and the transcript seems to be more abundant in larvae than in other developmental stages.

Conclusion: These results suggest that the F1538I mutation plays an important role in fenpropathrin resistance in citrus red mites. This is the first study of the sodium channel in P. citri and provides abundant information for further research on the mechanism of pyrethroid resistance.

Keywords: Panonychus citri; alternative splicing; knockdown resistance; mutation; sodium channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acaricides / pharmacology*
  • Amino Acid Sequence
  • Animals
  • Arthropod Proteins / genetics*
  • Arthropod Proteins / metabolism
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • DNA, Complementary / metabolism
  • Drug Resistance
  • Gene Expression Regulation, Developmental / drug effects
  • Larva / drug effects
  • Molecular Sequence Data
  • Nymph / drug effects
  • Phylogeny
  • Point Mutation / drug effects
  • Pyrethrins / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sequence Alignment
  • Sodium Channels / genetics*
  • Sodium Channels / metabolism
  • Tetranychidae / drug effects*
  • Tetranychidae / genetics*
  • Tetranychidae / metabolism

Substances

  • Acaricides
  • Arthropod Proteins
  • DNA, Complementary
  • Pyrethrins
  • RNA, Messenger
  • Sodium Channels
  • fenpropathrin

Associated data

  • GENBANK/KF646792