Biochemical studies of insecticide resistance in Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus (Diptera: Culicidae) in Thailand.

Abstract

Biochemical analysis was performed on field caught Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus (Diptera: Culicidae) mosquitoes to determine activities of enzymes including mixed function oxidases (MFO), nonspecific esterases (alpha- and beta-), glutathione-S-transferases (GST), and insensitive acetylcholinesterase (AChE). Biochemical tests were performed on F1 generation of Ae. aegypti field caught mosquitoes, while in Ae. albopictus F2 progenies were used. Twenty-six samples of Ae. aegypti mosquito were collected from areas across different parts of Thailand including Bangkok (central), and the provinces of Chiang Rai (north), Nakhon Sawan (north-central), Nakhon Ratchasrima (northeast), Chonburi (east), Chanthaburi (east), and Songkhla (south). Eight wild caught samples of Ae. albopictus were from Songkhla, Nakhon Sawan, Nakhon Ratchasrima and Kanchanaburi (west) provinces. The susceptibility to pyrethroids (deltamethrin, permethrin), organophosphate (fenitrothion) and carbamate (propoxur) insecticides were revealed in these samples. The biochemical test results were compared with those of the susceptible Bora (French Polynesia) strain. There was significant enhancement of MFO in pyrethroid resistant Ae. aegypti samples, except those from Songkhla and Hauykwang district in Bangkok. Biochemical assay results suggested that nonspecific esterases conferred fenitrothion resistance in Ae. aegypti in Nakhon Sawan, while insensitive AChE and/or nonspecific esterases could play role in fenitrothion resistance in Nakhon Ratchasrima. There was no consistent association of GST with pyrethroid resistance in Ae. aegypti. Low enzyme activities found in Ae. aegypti in Songkhla and in Ae. albopictus corresponded to their insecticide susceptibility status. The increased enzyme activity in field samples reflecting local history of insecticide employment was discussed.