Long-lasting control of Anopheles arabiensis by a single spray application of micro-encapsulated pirimiphos-methyl (Actellic® 300 CS)
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Richard M Oxborough1, Jovin Kitau, Rebecca Jones
1Department of Disease Control, London School of Hygiene and Tropical Medicine (LSHTM), London, UK. oxandbull@hotmail.com.
Background:
Pyrethroid-resistant mosquitoes are an increasing threat to malaria vector control. The Global Plan for Insecticide Resistance Management (GPIRM) recommends rotation of non-pyrethroid insecticides for indoor residual spraying (IRS). The options from other classes are limited. The carbamate bendiocarb and the organophosphate pirimiphos-methyl (p-methyl) emulsifiable concentrate (EC) have a short residual duration of action, resulting in increased costs due to multiple spray cycles, and user fatigue. Encapsulation (CS) technology was used to extend the residual performance of p-methyl.
Methods:
Two novel p-methyl CS formulations were evaluated alongside the existing EC in laboratory bioassays and experimental hut trials in Tanzania between 2008-2010. Bioassays were carried out monthly on sprayed substrates of mud, concrete, plywood, and palm thatch to assess residual activity. Experimental huts were used to assess efficacy against wild free-flying Anopheles arabiensis, in terms of insecticide-induced mortality and blood-feeding inhibition.
Results:
In laboratory bioassays of An. arabiensis and Culex quinquefasciatus both CS formulations produced high rates of mortality for significantly longer than the EC formulation on all substrates. On mud, the best performing CS killed >80% of An. arabiensis for five months and >50% for eight months, compared with one and two months, respectively, for the EC. In monthly bioassays of experimental hut walls the EC was ineffective shortly after spraying, while the best CS formulation killed more than 80% of An. arabiensis for five months on mud, and seven months on concrete. In experimental huts both CS and EC formulations killed high proportions of free-flying wild An. arabiensis for up to 12 months after spraying. There was no significant difference between treatments. All treatments provided considerable personal protection, with blood-feeding inhibition ranging from 9-49% over time.
Conclusions:
The long residual performance of p-methyl CS was consistent in bioassays and experimental huts. The CS outperformed the EC in laboratory and hut bioassays but the EC longevity in huts was unexpected. Long-lasting p-methyl CS formulations should be more effective than both p-methyl EC and bendiocarb considering a single spray could be sufficient for annual malaria control. IRS with p-methyl 300 CS is a timely addition to the limited portfolio of long-lasting residual insecticides.
Insights
Encapsulated pirimiphos-methyl (p-methyl) insecticide formulations show extended residual activity against malaria mosquitoes. This new technology offers a longer-lasting solution for indoor residual spraying (IRS), improving malaria vector control.
Area of Science:
- Entomology
- Public Health
- Vector Control
Background:
- Pyrethroid-resistant mosquitoes pose a significant challenge to malaria vector control efforts.
- Limited non-pyrethroid insecticide options exist for indoor residual spraying (IRS), necessitating new solutions.
- Existing carbamate and organophosphate insecticides have short residual durations, increasing costs and user burden.
Purpose of the Study:
- To evaluate the extended residual performance of novel encapsulated (CS) formulations of pirimiphos-methyl (p-methyl).
- To compare the efficacy of p-methyl CS formulations against the standard emulsifiable concentrate (EC) formulation.
- To assess the effectiveness of these formulations against wild, free-flying Anopheles arabiensis mosquitoes.
Main Methods:
- Laboratory bioassays were conducted monthly on various substrates (mud, concrete, plywood, palm thatch) to assess residual activity.
- Experimental hut trials were performed in Tanzania to evaluate efficacy against wild Anopheles arabiensis.
- Key metrics included insecticide-induced mortality and blood-feeding inhibition.
Main Results:
- Both p-methyl CS formulations demonstrated significantly longer residual activity than the EC formulation in laboratory bioassays.
- The best-performing CS formulation maintained high mortality rates (>80%) for up to eight months on mud substrates.
- In experimental huts, CS formulations provided effective control for extended periods, with some treatments showing efficacy up to 12 months.
Conclusions:
- The long residual performance of p-methyl CS formulations was consistent across laboratory and field evaluations.
- p-methyl CS formulations offer a more effective and potentially cost-efficient alternative to p-methyl EC and bendiocarb for IRS.
- p-methyl 300 CS represents a valuable addition to the limited arsenal of long-lasting residual insecticides for malaria control.
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