Journal
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
Volume 187, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pestbp.2022.105186
Keywords
Musca domestica; Propoxur; CYP6G4; Insecticide resistance; Metabolism; GAL4/UAS
Categories
Funding
- National Natural Science Foundation of China [31672371, 30671383]
- Natural Science Foundation of Beijing [5142014]
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This study investigates the involvement of overexpressed cytochrome P450 enzyme CYP6G4 in the metabolism and resistance of the insecticide propoxur in house flies. The researchers found that CYP6G4 could transform propoxur and identified six metabolites. Furthermore, they demonstrated that overexpression of CYP6G4 in fruit flies increased their tolerance to propoxur, indicating its role in resistance.
The house fly (Musca domestica L.) (Diptera: Muscidae) is a global vector that can transmit >250 human and animal diseases. The control of house flies has heavily relied on the application of various chemical insecticides. The carbamate insecticide propoxur has been widely used for the control of house flies, and resistance to propoxur has been documented in many house fly populations worldwide. Previous studies have identified several propoxur resistance-conferring mutations in the target protein acetylcholinesterase; however, the molecular basis for metabolic resistance to propoxur remains unknown. In this study, we investigated the involvement of CYP6G4, a cytochrome P450 overexpressed in many insecticide resistant populations of Musca domestica, in propoxur metabolism and resistance by using combined approaches of recombinant protein-based insecticide metabolism and the Drosophila GAL4/UAS transgenic system. The recombinant CYP6G4 and its redox partners (NADPH-dependent cytochrome P450 reductase and cytochrome b5) were functionally expressed in Escherichia coli. Metabolism experiments showed that CYP6G4 was able to transform propoxur with a turnover rate of around 0.79 min(-1). Six metabolites were putatively identified, suggesting that CYP6G4 could metabolize propoxur via hydroxylation, O-depropylation and N-demethylation. Moreover, bioassay results showed that ectopic overexpression of CYP6G4 in fruit flies significantly increased their tolerance to propoxur. Our in vivo and in vitro data convincingly demonstrate that CYP6G4 contributes to propoxur metabolism and resistance.
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