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Multiple insecticide resistance in the major malaria vector Anopheles funestus in southern Ghana: implications for malaria control

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dc.contributor.author Riveron, Jacob M.
dc.contributor.author Osae, Michael
dc.contributor.author Egyir-Yawson, Alexander
dc.contributor.author Irving, Helen
dc.contributor.author Ibrahim, Sulaiman S.
dc.contributor.author Wondji, Charles S.
dc.date.accessioned 2021-07-01T13:38:54Z
dc.date.available 2021-07-01T13:38:54Z
dc.date.issued 2016
dc.identifier.issn 23105496
dc.identifier.uri http://hdl.handle.net/123456789/5567
dc.description 9p:, ill. en_US
dc.description.abstract Background: Understanding the dynamics of insecticide resistance in African malaria vectors is crucial for successful implementation of resistance management strategies in the continent. his study reports a high and multiple insecticide resistance in Anopheles funestus from southern Ghana which could compromise the Malaria Operational Plan in this country, if not tackled. Adult Anopheles mosquitoes were collected in Obuasi and Adawukwa, in southern Ghana. Plasmodium infection rates, susceptibility to the main insecticides used in public health and the molecular basis of insecticide resistance were established. Results:An. funestus (sensu stricto) (s.s.) was the predominant mosquito species found resting inside the houses in Obuasi, while at Adawukwa it was found together withAn. coluzzii. Parasite rates were high inAn. funestus (s.s.) populations from both localities, withPlasmodium infection rates greater than 12.5 %. Both,An. funestus (s.s.) and An. coluzzii, from the two sites exhibited high resistance to the insecticide from various classes including the pyrethroids, carbamates and DDT, but remained fully susceptible to the organophosphates. A preliminary characterization of the underlying molecular mechanisms of resistance inAn. funestus (s.s.) populations from both sites revealed that CYP6P9a, CYP6P9b,CYP6M7and GSTe2 genes are upregulated, markedly higher in Obuasi (between 3.35 and 1.83 times) than in Adawukwa population. he frequency of L119F-GSTe2 and A296S-RDL resistance markers were also higher in Obuasi (42.5 and 68.95 % higher), compared withAn. funestus (s.s.) populations from Adawukwa. These findings suggest that the similar resistance pattern observed in both An. funestus (s.s.) populations are driven by different mechanisms. Conclusions: Resistance to multiple insecticides in public health use is present in malaria vectors from Ghana with major resistance genes already operating in the field. This should be taken into consideration in the design of resistance management strategies to avoid operational failure en_US
dc.language.iso en en_US
dc.publisher University of Cape Coast en_US
dc.subject Malaria en_US
dc.subject Insecticide resistance en_US
dc.subject Vector control en_US
dc.subject An. Funestus en_US
dc.subject An. Gambiae en_US
dc.subject An. Coluzzii en_US
dc.subject Ghana en_US
dc.title Multiple insecticide resistance in the major malaria vector Anopheles funestus in southern Ghana: implications for malaria control en_US
dc.type Article en_US


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