Control of insecticide resistance in a field population of houseflies,Musca domestica, by releasing susceptible flies

Abstract Background: Although there is a vast literature concerning insecticide resistance (IR) in Plasmodium vectors from African and Asian continents, similar studies with Neotropical anophelines are scares. Herein we evaluated the IR profile of Anopheles albitarsis s.s. of a laboratory colony and a natural population collected around a rice plantation field. The laboratory colony is original from a collection performed in this same region more than two decades ago. Methods: We collected An. albitarsis females while resting after blood feeding, around rice field plantations in Massaranduba, SC, Brazil. These females laid their eggs in the laboratory, and the larvae were raised in parallel with our lab colony. To be sure about the field samples’ taxonomic status, we amplified and sequenced the mitochondrial COI gene of a sampling of field captured mosquitoes. We performed a simplified knockdown test with larvae exposed to permethrin and deltamethrin and submitted adult females to a WHO like tube test with the pyrethroids permethrin, deltamethrin, and etofenprox, in addition to the organophosphate malathion. A segment of the voltage-gated sodium channel gene (NaV) was amplified and cloned. Based on the observed sequences, we developed a TaqMan genotyping assay for the variation L1014F and calculated the genotypic and allelic frequencies concerning this SNP in the field population.Results: The COI analyses confirmed the taxonomic status of An. albitarsis s.s in laboratory and field samples. The field population was resistant to pyrethroids but not to malathion. We observed the substitutions L1019R, F1020S, and the classical kdr L1014F in the NaV gene. This classical kdr allele was present under low frequencies in the overall field population (2%), although more frequent in pyrethroid-resistant insects.Conclusions: The An. albitarsis s.s. population from Massaranduba was resistant to pyrethroids, likely due to selection pressure exerted by agrochemical pesticides. We registered the classical kdr mutation in a Brazilian Anopheles species for the first time. Further investigations are necessary to disclose additional resistance mechanisms.

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Activities of detoxifying enzymes in adults of houseflies Musca domestica L. selected with chlorfenapyr

Biomics ◽

10.31301/2221-6197.bmcs.2020-43 ◽

2020 ◽

Vol 12 (4) ◽

pp. 492-503

Author(s):

E.A. Silivanova ◽

P.A. Shumilova ◽

M.A. Levchenko

Keyword(s):

Alkaline Phosphatase ◽

Insecticide Resistance ◽

Musca Domestica ◽

Glutathione S Transferase ◽

Detoxifying Enzymes ◽

Resistance Development ◽

Phosphatase Activities ◽

Biochemical Mechanisms ◽

Males And Females

In insects, biochemical mechanisms of insecticide resistance base on increasing of activities of main detoxyfying enzymes – monooxygenases, nonspesific esterases, and glutathion-S-transferases. Currently, the progress of resistance development and the degree of contributing enzymes to resistance in insects have been studied for certain insecticides. The goal of this study was to assess activities of monooxygenase, carboxylesterase, glutathione-S-transferase, and alkaline phosphatase in females and males housefly Musca domestica in the second, fourth, sixth, eighth and tenth generations of the chlorfenapyr-selected strain. Evaluation of chlorfenapyr susceptibility showed that adults M. domestica in tenth generations was tolerating to chlorfenapyr as the resistance ration value was 3.6. In certain generations of chlorfenapyr-selected strain M. domestica, monooxygenase activities in males and females were 1.4-2.1 times more, and alkaline phosphatase activities in females were 2.3-2.7 times more than that in control insects. Glutathione-S-transferase activities had no significant differences in adults M. domestica of control and chlorfenapyr-selected strains. For chlorfenapyr-selected strain M. domestica, activities of monooxygenase, carboxylesterase, and alkaline phosphatase differed in males and females of same generations that suggests that mode and pattern of resistance development might be sex-specific in this specie.

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Activities of Select Enzymes Involved in Insecticide Resistance in Spinosad-Resistant and -Susceptible Strains of Musca domestica (Diptera: Muscidae)

Journal of Medical Entomology ◽

10.1093/jme/tjz168 ◽

2019 ◽

Author(s):

Hafiz Azhar Ali Khan ◽

Waseem Akram ◽

Sajid Ali

Keyword(s):

Insecticide Resistance ◽

Musca Domestica ◽

Enzyme Activities ◽

Susceptible Strain ◽

Detoxifying Enzymes ◽

Mechanism Of Resistance ◽

Mixed Function Oxidases ◽

Glutathione S Transferases

Abstract A Musca domestica L. strain collected from Pakistan has recently been shown to be resistant to spinosad; however, there is scarce information about the mechanism of resistance. For this reason, we explored whether a metabolic-based mechanism was responsible by analyzing the activities of the metabolic detoxifying enzymes, carboxylesterases, glutathione S-transferases, and mixed-function oxidases, in both a spinosad-selected (Spin-SEL) strain of M. domestica and a susceptible counterpart (Lab-susceptible). The results revealed that both strains were statistically at par in terms of enzyme activities. The activity of carboxylesterases in the Lab-susceptible strain was 78.17 ± 3.06 in comparison to 79.16 ± 3.31 nmol min−1 mg−1 in the Spin-SEL strain. The activity of mixed-function oxidases was 51.58 ± 4.20 in the Lab-susceptible strain, whereas 54.33 ± 4.08 pmol min−1 mg−1 was recorded in the Spin-SEL strain. The activity of glutathione S-transferases was 86.50 ± 4.59 (Lab-susceptible) and 90.33 ± 2.81 nmol min−1 mg−1 (Spin-SEL). These results revealed that the studied enzymes might not be responsible for spinosad resistance in the studied strain of M. domestica. Therefore, studies should be extended to find out other possible mechanisms of spinosad resistance.

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