scholarly journals Electrophoretic Analysis of Nonspecific Esterases and Acetylcholinesterases from the Housefly, Musca domestica L. (Diptera : Muscidae), with Reference to Organophosphorus Insecticide Resistance

1983 ◽  
Vol 18 (4) ◽  
pp. 447-455 ◽  
Author(s):  
Masashi UGAKI ◽  
Takashi ABE ◽  
Jun-ichi FUKAMI ◽  
Toshio SHONO
1992 ◽  
Vol 71 (3) ◽  
pp. 121-134 ◽  
Author(s):  
John S. Prevec ◽  
Nicholas Darko Okoampah ◽  
R. A. Morton

Biomics ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 492-503
Author(s):  
E.A. Silivanova ◽  
P.A. Shumilova ◽  
M.A. Levchenko

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.


Author(s):  
Hafiz Azhar Ali Khan ◽  
Waseem Akram ◽  
Sajid Ali

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.


1966 ◽  
Vol 14 (7) ◽  
pp. 560-566 ◽  
Author(s):  
BRUCE FRIEDMAN ◽  
DONALD S. STRACHAN ◽  
MAYNARD M. DEWEY

With α-naphthyl butyrate and α-naphthyl acetate as substrates nonspecific esterase activity was demonstrated in both the crypt epithelium and epithelium covering the villus of the small intestine of the rat. This distribution of enzymatic activity does not correspond to the distribution of the so-called "absorptive epithelium." Starch gel electrophoretic analysis of intestinal homogenates showed a spectrum of enzymatically active fractions which hydrolyzed both substrates. The number of enzymic fractions and their electrophoretic mobilities were the same with both substrates, but the butyrate ester was hydrolyzed 2.5 times more rapidly than the acetate ester. These observations are discussed in relation to the rapid differentiation which occurs as cells migrate from the intestinal crypts onto the surface of the villus.


1986 ◽  
Vol 76 (2) ◽  
pp. 297-302 ◽  
Author(s):  
I. Denholm ◽  
R. M. Sawicki ◽  
A. W. Farnham ◽  
Jean C. White

AbstractAn inexpensive and versatile method for maintaining age-structured Musca domestica L. populations for studies on the evolution of insecticide resistance is described. Adult flies are kept in spacious aluminium cages in which age-structuring is maintained by the thrice-weekly addition of pupae bred from eggs collected from within the cages. The population size is regulated in a density-independent manner by constraining the input of pupae to that necessary to maintain the required equilibrium density of adults within a cage. Adult numbers are monitored by photographing from outside the cage flies settled on a grid etched on the rear wall, and by converting this grid count to an estimate of population size using a calculated regression line. Observed changes in fly numbers in a cage accorded well with those predicted by a computer model using empirical data on larval productivity, and the emergence and survivorship schedules of adult flies. Since a variety of insecticide control regimes can be applied within the cage, this system enables an adequate yet tractable simulation of selection for resistance by insecticides under field conditions.


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