4.8 Article

Reduced proinsecticide activation by cytochrome P450 confers coumaphos resistance in the major bee parasite Varroa destructor

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2020380118

Keywords

pesticide; honey bee; selectivity; resistance management; CYPome

Funding

  1. Greek national funds through the Public Investments Program of the General Secretariat for Research and Technology, under the Emblematicction The Bee Road [2018SE01300000]
  2. European Union (European Social Fund) through the Operational Programme Human Resources Development, Education and Lifelong Learning [MIS-5000432]
  3. Research Foundation Flanders [1274917N, G053815N]
  4. European Research Council under the European Union's Horizon 2020 research and innovation program [772026]
  5. European Research Council (ERC) [772026] Funding Source: European Research Council (ERC)

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Varroa destructor mites from the island Andros exhibit high levels of resistance to coumaphos, with reduced activation of the proinsecticide by a cytochrome P450 enzyme being the main resistance mechanism. Transcriptome analysis revealed overexpression of CYP4DP24 and underexpression of CYP3012A6 and CYP4EP4 in resistant mites. RNA interference of CYP4EP4 in susceptible mites prevented coumaphos activation and decreased toxicity, suggesting a potential solution for overcoming resistance in Varroa destructor populations.
Varroa destructor is one of the main problems in modern beekeeping. Highly selective acaricides with low toxicity to bees are used internationally to control this mite. One of the key acaricides is the organophosphorus (OP) proinsecticide coumaphos, that becomes toxic after enzymatic activation inside Varroa. We show here that mites from the island Andros (AN-CR) exhibit high levels of coumaphos resistance. Resistance is not mediated by decreased coumaphos uptake, target-site resistance, or increased detoxification. Reduced proinsecticide activation by a cytochrome P450 enzyme was the main resistance mechanism, a powerful and rarely encountered evolutionary solution to insecticide selection pressure. After treatment with sublethal doses of [C-14] coumaphos, susceptible mite extracts had substantial amounts of coroxon, the activated metabolite of coumaphos, while resistant mites had only trace amounts. This indicates a suppression of the P450 (CYP)-mediated activation step in the AN-CR mites. Bioassays with coroxon to bypass the activation step showed that resistance was dramatically reduced. There are 26 CYPs present in the V. destructor genome. Transcriptome analysis revealed overexpression in resistant mites of CYP4DP24 and underexpression of CYP3012A6 and CYP4EP4. RNA interference of CYP4EP4 in the susceptible population, to mimic underexpression seen in the resistant mites, prevented coumaphos activation and decreased coumaphos toxicity.

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