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- W4246508470 abstract "Abstract Background : Mosquito control based on chemical insecticides is considered as an important element in the current global strategies for the control of mosquito-borne diseases. Unfortunately, the development of insecticide resistance of important vector mosquito species jeopardizes the effectiveness of insecticide-based mosquito control. As opposed to target site resistance, other mechanisms are far from being fully understood. Results : Susceptible strain of Cx. pipiens pallen showed elevated resistance levels to after 25 generations insecticide-selected, through bioinformatics analysis allowed detecting 2,502 proteins, of which 1513 were differentially expression in insecticide-selected strains as compared to the susceptible strain. Finally, midgut differential expression protein profiles and 62 proteins were selected for verification of differential expression using parallel reaction monitoring strategy. Conclusions Significant molecular resources were developed for Cx. pipiens pallen potential candidates involved in metabolic resistance as well as those participating in lower penetration or sequestration of insecticide. Global protein profiles of change to three insecticide strains combined with midgut profiles revealed multiple insecticide resistance mechanisms operate simultaneously in resistant insects of Cx. pipiens pallens . Future research that is targeted towards RNA interference on the identified metabolic targets such as cuticular, cytochrome P450s and glutathione S-transferase proteins could lay the foundation for a better understanding of the genetic basis of insecticide resistance in Cx. pipiens pallen ." @default.
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- W4246508470 date "2020-08-01" @default.
- W4246508470 modified "2023-10-16" @default.
- W4246508470 title "Comparative proteomics reveals complex insecticides-associated resistance mechanism of Culex pipiens pallens Coquillett" @default.
- W4246508470 doi "https://doi.org/10.21203/rs.3.rs-45444/v1" @default.
- W4246508470 hasPublicationYear "2020" @default.
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