Abstract

BackgroundInsecticides are critical components of malaria control programmes. In a variety of insect species, temperature plays a fundamental role in determining the outcome of insecticide exposure. However, surprisingly little is known about how temperature affects the efficacy of chemical interventions against malaria vectors.MethodsAnopheles stephensi, with no recent history of insecticide exposure, were exposed to the organophosphate malathion or the pyrethroid permethrin at 12, 18, 22, or 26°C, using the WHO tube resistance-monitoring assay. To evaluate the effect of pre-exposure temperature on susceptibility, adult mosquitoes were kept at 18 or 26°C until just before exposure, and then moved to the opposite temperature. Twenty-four hours after exposure, mosquitoes exposed at <26°C were moved to 26°C and recovery was observed. Susceptibility was assessed in terms of survival 24 hours after exposure; data were analysed as generalized linear models using a binomial error distribution and logit link function.ResultsLowering the exposure temperature from the laboratory standard 26°C can strongly reduce the susceptibility of female An. stephensi to the WHO resistance-discriminating concentration of malathion (χ2df=3 = 29.0, p < 0.001). While the susceptibility of these mosquitoes to the resistance-discriminating concentration of permethrin was not as strongly temperature-dependent, recovery was observed in mosquitoes moved from 12, 18 or 22°C to 26°C 24 hours after exposure. For permethrin especially, the thermal history of the mosquito was important in determining the ultimate outcome of insecticide exposure for survival (permethrin: pre-exposure temperature: F1,29 = 14.2, p < 0.001; exposure temp: F1,29 = 1.1, p = 0.3; concentration: F1,29 = 85.2, p < 0.001; exposure temp x conc: F1,29 = 5.8, p = 0.02). The effect of acclimation temperature on malathion susceptibility depended on the exposure temperature (exposure temp: F1,79 = 98.4, p < 0.001; pre-exposure temp: F1,79 = 0.03, p = 0.9; pre-exp temp x exp temp F1,79 = 6.0, p = 0.02).ConclusionsA single population of An. stephensi could be classified by WHO criteria as susceptible or resistant to a given chemical, depending on the temperature at which the mosquitoes were exposed. Investigating the performance of vector control tools under different temperature conditions will augment the ability to better understand the epidemiological significance of insecticide resistance and select the most effective products for a given environment.

Highlights

  • Insecticides are critical components of malaria control programmes

  • The current study investigates how temperature affects knockdown and mortality of An. stephensi females following exposure to two classes of insecticide approved for use in public health: organophosphates and pyrethroids [22]

  • The results indicate that the single population of An. stephensi could be classified by World Health Organization (WHO) criteria as susceptible or resistant to a given chemical, depending on the temperature at which the mosquitoes were housed

Read more

Summary

Introduction

Insecticides are critical components of malaria control programmes. In a variety of insect species, temperature plays a fundamental role in determining the outcome of insecticide exposure. Surprisingly little is known about how temperature affects the efficacy of chemical interventions against malaria vectors. Chemical insecticides form the backbone of malaria vector control programmes. The effectiveness of chemical insecticides is being threatened by the widescale emergence of insecticide resistance [2,3,4]. The standard methodologies for monitoring and evaluating resistance use bioassay protocols developed by the WHO Pesticide Evaluation Scheme (WHOPES) to test the mortality of young (three- to five-day old) female mosquitoes following single, limited-time exposure to the relevant insecticide [5,6]. Determining the impact of current and future insecticides under realistic environmental conditions could be important for making informed decisions about which compound is likely to be effective under local epidemiological conditions [8]

Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.