Point mutations associated with organophosphate and carbamate resistance in Chinese strains of Culex pipiens quinquefasciatus (Diptera: Culicidae)

PLoS One. 2014 May 1;9(5):e95260. doi: 10.1371/journal.pone.0095260. eCollection 2014.

Abstract

Acetylcholinesterase resistance has been well documented in many insects, including several mosquito species. We tested the resistance of five wild, Chinese strains of the mosquito Culex pipiens quinquefasciatus to two kinds of pesticides, dichlorvos and propoxur. An acetylcholinesterase gene (ace1) was cloned and sequenced from a pooled sample of mosquitoes from these five strains and the amino acids of five positions were found to vary (V185M, G247S, A328S, A391T, and T682A). Analysis of the correlation between mutation frequencies and resistance levels (LC50) suggests that two point mutations, G247S (r2 = 0.732, P = 0.065) and A328S (r2 = 0.891, P = 0.016), are associated with resistance to propoxur but not to dichlorvos. Although the V185M mutation was not associated with either dichlorvos or propoxur resistance, its RS genotype frequency was correlated with propoxur resistance (r2 = 0.815, P = 0.036). And the HWE test showed the A328S mutation is linked with V185M, also with G247S mutation. This suggested that these three mutations may contribute synergistically to propoxur resistance. The T682A mutation was negatively correlated with propoxur (r2 = 0.788, P = 0.045) resistance. Knowledge of these mutations may help design strategies for managing pesticide resistance in wild mosquito populations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / chemistry
  • Acetylcholinesterase / genetics
  • Alleles
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carbamates / pharmacology*
  • Catalytic Domain
  • Cholinesterase Inhibitors / pharmacology
  • Culex / drug effects*
  • Culex / genetics*
  • Dichlorvos / pharmacology
  • Female
  • Gene Frequency
  • Genetic Linkage
  • Insecticide Resistance / genetics*
  • Linkage Disequilibrium
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation
  • Organophosphates / pharmacology*
  • Point Mutation*
  • Polymorphism, Genetic
  • Propoxur / pharmacology
  • Protein Conformation

Substances

  • Carbamates
  • Cholinesterase Inhibitors
  • Organophosphates
  • Dichlorvos
  • Propoxur
  • Acetylcholinesterase

Grants and funding

This work was funded by the foundation from the Infective Diseases Prevention and Cure Project of National Ministry of Public Health of China (No.2008ZX10004 and No.2012ZX10004219). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.