Abstract

Malaria is holoendemic in Ghana. The effectiveness of insecticide based vector control methods is hampered there by the development of insecticide resistance. Resistance to multiple classes of insecticide has previously been detected in a population of the major malaria vector Anopheles gambiae in the Obuasi region of Ghana. The establishment of a laboratory colony (GAH) using wild An. gambiae Sf orm material from Obuasi has enabled characterization of multiple insecticide resistance in the GAH colony as well as an appraisal of the effect of staggered larval time-to-hatch on the assortment of resistance phenotypes. Materials and methods Larval-time-to-hatch, characterized as either early (within four days of oviposition) or late hatch (four days or more post oviposition), was assessed in the GAH colony by selecting time-to-hatch sub-colonies. Crosses between the early and late hatch sub-colonies as well as intercrosses and subsequent back-crosses to the parental sub-colonies were conducted in an effort to establish the genetic basis for larval time-to-hatch. Insecticide resistance in the baseline colony as well as in the selected sub-colonies was characterized using standard WHO bioassays, synergist exposure assays and allele specific PCR assays designed to genotype loci carrying known insecticide resistance associated mutations. Result The GAH colony shows resistance to all classes of insecticide currently available for use in public health. Mechanisms of resistance to pyrethroids in GAH include monooxygenase and esterase mediated detoxification coupled with the L1014F kdr mutation. Resistance to DDT associated particularly closely with the assortment of L1014F kdr. Resistance to dieldrin associated closely with the rdl mutation while resistance to the carbamate bendiocarb associated closely with the ace-1 mutation. Cross-mating between the time-to-hatch phenotypes, supported by hybrid intercrosses and back-crossing of hybrids to the parental strains, gave ambiguous results suggesting that this genetic component may be multi-factorial. There was significant variation in the expression of insecticide resistance between the time-to-hatch phenotypes, suggesting that selection for time-to-hatch inadvertently affected the frequencies of those factors controlling insecticide resistance.

Highlights

  • Resistance to multiple classes of insecticide has previously been detected in a population of the major malaria vector Anopheles gambiae in the Obuasi region of Ghana

  • Crosses between the early and late hatch sub-colonies as well as intercrosses and subsequent back-crosses to the parental sub-colonies were conducted in an effort to establish the genetic basis for larval time-to-hatch

  • Mechanisms of resistance to pyrethroids in GAH include monooxygenase and esterase mediated detoxification coupled with the L1014F kdr mutation

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Summary

Background

The effectiveness of insecticide based vector control methods is hampered there by the development of insecticide resistance. Resistance to multiple classes of insecticide has previously been detected in a population of the major malaria vector Anopheles gambiae in the Obuasi region of Ghana. The establishment of a laboratory colony (GAH) using wild An. gambiae S form material from Obuasi has enabled characterization of multiple insecticide resistance in the GAH colony as well as an appraisal of the effect of staggered larval time-to-hatch on the assortment of resistance phenotypes

Materials and methods
Result
Conclusion
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