Literature DB >> 9737593

Resistance management strategies in malaria vector mosquito control. Baseline data for a large-scale field trial against Anopheles albimanus in Mexico.

R P Penilla1, A D Rodríguez, J Hemingway, J L Torres, J I Arredondo-Jiménez, M H Rodríguez.   

Abstract

A high level of DDT resistance and low levels of resistance to organophosphorus, carbamate and pyrethroid insecticides were detected by discriminating dose assays in field populations of Anopheles albimanus in Chiapas, southern Mexico, prior to a large-scale resistance management project described by Hemingway et al. (1997). Biochemical assays showed that the DDT resistance was caused by elevated levels of glutathione S-transferase (GST) activity leading to increased rates of metabolism of DDT to DDE. The numbers of individuals with elevated GST and DDT resistance were well correlated, suggesting that this is the only major DDT resistance mechanism in this population. The carbamate resistance in this population is conferred by an altered acetylcholinesterase (AChE)-based resistance mechanism. The level of resistance observed in the bioassays correlates with the frequency of individuals homozygous for the altered AChE allele. This suggests that the level of resistance conferred by this mechanism in its heterozygous state is below the level of detection by the WHO carbamate discriminating dosage bioassay. The low levels of organophosphate (OP) and pyrethroid resistance could be conferred by either the elevated esterase or monooxygenase enzymes. The esterases were elevated only with the substrate pNPA, and are unlikely to be causing broad spectrum OP resistance. The altered AChE mechanism may also be contributing to the OP but not the pyrethroid resistance. Significant differences in resistance gene frequencies were obtained from the F1 mosquitoes resulting from adults obtained by different collection methods. This may be caused by different insecticide selection pressures on the insects immediately prior to collection, or may be an indication that the indoor- and outdoor-resting A. albimanus collections are not from a randomly mating single population. The underlying genetic variability of the populations is currently being investigated by molecular methods.

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Year:  1998        PMID: 9737593     DOI: 10.1046/j.1365-2915.1998.00123.x

Source DB:  PubMed          Journal:  Med Vet Entomol        ISSN: 0269-283X            Impact factor:   2.739


  47 in total

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4.  Mechanisms of pyrethroid resistance in Aedes (Stegomyia) aegypti from Colombia.

Authors:  Angélica Aponte; R Patricia Penilla; Américo D Rodríguez; Clara B Ocampo
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5.  High level of pyrethroid resistance in an Anopheles funestus population of the Chokwe District in Mozambique.

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Journal:  PLoS One       Date:  2010-06-08       Impact factor: 3.240

6.  Pyrethroid resistance in an Anopheles funestus population from Uganda.

Authors:  John C Morgan; Helen Irving; Loyce M Okedi; Andrew Steven; Charles S Wondji
Journal:  PLoS One       Date:  2010-07-29       Impact factor: 3.240

7.  Recent rapid rise of a permethrin knock down resistance allele in Aedes aegypti in México.

Authors:  Gustavo Ponce García; Adriana E Flores; Ildefonso Fernández-Salas; Karla Saavedra-Rodríguez; Guadalupe Reyes-Solis; Saul Lozano-Fuentes; J Guillermo Bond; Mauricio Casas-Martínez; Janine M Ramsey; Julián García-Rejón; Marco Domínguez-Galera; Hilary Ranson; Janet Hemingway; Lars Eisen; William C Black IV
Journal:  PLoS Negl Trop Dis       Date:  2009-10-13

8.  Absence of knockdown resistance suggests metabolic resistance in the main malaria vectors of the Mekong region.

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9.  Reduced efficacy of insecticide-treated nets and indoor residual spraying for malaria control in pyrethroid resistance area, Benin.

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10.  Pyrethroid resistance in the major malaria vector Anopheles arabiensis from Gwave, a malaria-endemic area in Zimbabwe.

Authors:  Givemore Munhenga; Hieronymo T Masendu; Basil D Brooke; Richard H Hunt; Lizette K Koekemoer
Journal:  Malar J       Date:  2008-11-28       Impact factor: 2.979

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