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A mutation in the intracellular loop III/IV of mosquito sodium channel synergizes the effect of mutations in helix IIS6 on pyrethroid resistance.

Publication ,  Journal Article
Wang, L; Nomura, Y; Du, Y; Liu, N; Zhorov, BS; Dong, K
Published in: Molecular pharmacology
January 2015

Activation and inactivation of voltage-gated sodium channels are critical for proper electrical signaling in excitable cells. Pyrethroid insecticides promote activation and inhibit inactivation of sodium channels, resulting in prolonged opening of sodium channels. They preferably bind to the open state of the sodium channel by interacting with two distinct receptor sites, pyrethroid receptor sites PyR1 and PyR2, formed by the interfaces of domains II/III and I/II, respectively. Specific mutations in PyR1 or PyR2 confer pyrethroid resistance in various arthropod pests and disease vectors. Recently, a unique mutation, N(1575)Y, in the cytoplasmic loop linking domains III and IV (LIII/IV) was found to coexist with a PyR2 mutation, L(1014)F in IIS6, in pyrethroid-resistant populations of Anopheles gambiae. To examine the role of this mutation in pyrethroid resistance, N(1575)Y alone or N(1575)Y + L(1014)F were introduced into an Aedes aegypti sodium channel, AaNav1-1, and the mutants were functionally examined in Xenopus oocytes. N(1575)Y did not alter AaNav1-1 sensitivity to pyrethroids. However, the N(1575)Y + L(1014)F double mutant was more resistant to pyrethroids than the L(1014)F mutant channel. Further mutational analysis showed that N(1575)Y could also synergize the effect of L(1014)S/W, but not L(1014)G or other pyrethroid-resistant mutations in IS6 or IIS6. Computer modeling predicts that N(1575)Y allosterically alters PyR2 via a small shift of IIS6. Our findings provide the molecular basis for the coexistence of N(1575)Y with L(1014)F in pyrethroid resistance, and suggest an allosteric interaction between IIS6 and LIII/IV in the sodium channel.

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Published In

Molecular pharmacology

DOI

EISSN

1521-0111

ISSN

0026-895X

Publication Date

January 2015

Volume

87

Issue

3

Start / End Page

421 / 429

Related Subject Headings

  • Xenopus laevis
  • Sodium Channels
  • Pyrethrins
  • Protein Structure, Secondary
  • Pharmacology & Pharmacy
  • Mutation
  • Membrane Potentials
  • Insecticides
  • Female
  • Drug Resistance
 

Citation

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Wang, L., Nomura, Y., Du, Y., Liu, N., Zhorov, B. S., & Dong, K. (2015). A mutation in the intracellular loop III/IV of mosquito sodium channel synergizes the effect of mutations in helix IIS6 on pyrethroid resistance. Molecular Pharmacology, 87(3), 421–429. https://doi.org/10.1124/mol.114.094730
Wang, Lingxin, Yoshiko Nomura, Yuzhe Du, Nannan Liu, Boris S. Zhorov, and Ke Dong. “A mutation in the intracellular loop III/IV of mosquito sodium channel synergizes the effect of mutations in helix IIS6 on pyrethroid resistance.Molecular Pharmacology 87, no. 3 (January 2015): 421–29. https://doi.org/10.1124/mol.114.094730.
Wang L, Nomura Y, Du Y, Liu N, Zhorov BS, Dong K. A mutation in the intracellular loop III/IV of mosquito sodium channel synergizes the effect of mutations in helix IIS6 on pyrethroid resistance. Molecular pharmacology. 2015 Jan;87(3):421–9.
Wang, Lingxin, et al. “A mutation in the intracellular loop III/IV of mosquito sodium channel synergizes the effect of mutations in helix IIS6 on pyrethroid resistance.Molecular Pharmacology, vol. 87, no. 3, Jan. 2015, pp. 421–29. Epmc, doi:10.1124/mol.114.094730.
Wang L, Nomura Y, Du Y, Liu N, Zhorov BS, Dong K. A mutation in the intracellular loop III/IV of mosquito sodium channel synergizes the effect of mutations in helix IIS6 on pyrethroid resistance. Molecular pharmacology. 2015 Jan;87(3):421–429.
Journal cover image

Published In

Molecular pharmacology

DOI

EISSN

1521-0111

ISSN

0026-895X

Publication Date

January 2015

Volume

87

Issue

3

Start / End Page

421 / 429

Related Subject Headings

  • Xenopus laevis
  • Sodium Channels
  • Pyrethrins
  • Protein Structure, Secondary
  • Pharmacology & Pharmacy
  • Mutation
  • Membrane Potentials
  • Insecticides
  • Female
  • Drug Resistance