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      Development of resistance to chlorantraniliprole represses sex pheromone responses in male Plutella xylostella (L.)

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          Abstract

          The diamondback moth (DBM), Plutella xylostella (L.), is a serious pest that feeds on cruciferous crops. Prolonged exposure to insecticides has led to increased resistance and biological fitness alterations, such as reduced sensitivity to pheromones. However, the mechanisms underlying the influence of insecticides on sex pheromone recognition in male moths have not been elucidated. In this study, we found that male adults from the NIL strain (a chlorantraniliprole-resistant strain) showed decreased responses to sex pheromones at both the behavioral and electrophysiological levels compared to the SS strain (a susceptible strain) and the relative expression of the two pheromone-binding protein (PBP) genes ( PxPBP1 and PxPBP2) was downregulated in NIL compared to SS. Furthermore, downregulation of PxPBP1 and PxPBP2 by RNAi inhibited the responses of male moths to the sex pheromone at both the electrophysiological and behavioral levels. Fluorescence binding assays, homology modeling and molecular docking indicated that chlorantraniliprole could robustly bind both PxPBP1 and PxPBP2. The results indicated that the development of resistance to chlorantraniliprole reduced the response of DBM males to sex pheromones through the binding and downregulation of PxPBP1 and PxPBP2. This work provides new evidence for understanding the trade-offs between insecticide resistance and chemical communication as well as the fitness cost of insecticide resistance, in insects.

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          Most cited references51

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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              Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans.

              Experimental introduction of RNA into cells can be used in certain biological systems to interfere with the function of an endogenous gene. Such effects have been proposed to result from a simple antisense mechanism that depends on hybridization between the injected RNA and endogenous messenger RNA transcripts. RNA interference has been used in the nematode Caenorhabditis elegans to manipulate gene expression. Here we investigate the requirements for structure and delivery of the interfering RNA. To our surprise, we found that double-stranded RNA was substantially more effective at producing interference than was either strand individually. After injection into adult animals, purified single strands had at most a modest effect, whereas double-stranded mixtures caused potent and specific interference. The effects of this interference were evident in both the injected animals and their progeny. Only a few molecules of injected double-stranded RNA were required per affected cell, arguing against stochiometric interference with endogenous mRNA and suggesting that there could be a catalytic or amplification component in the interference process.
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                Author and article information

                Journal
                entomologia
                Entomologia Generalis
                Journal of General and Applied Entomology - Zeitschrift für Allgemeine und Angewandte Entomologie
                entomologia
                Schweizerbart Science Publishers (Stuttgart, Germany http://www.schweizerbart.com/ mail@ 123456schweizerbart.de )
                0171-8177
                04 October 2021
                7 December 2021
                : 41
                : 6
                : 615-625
                Affiliations
                Department of Entomology, China Agricultural University, Beijing, 100193, P. R. China
                Author notes
                Article
                100301 1359
                10.1127/entomologia/2021/1359
                c35699ea-c472-43eb-b68a-1774ca8b8a93
                Copyright © 2021 E. Schweizerbart’sche Verlagsbuchhandlung, 70176 Stuttgart, Germany
                History
                : 01 May 2021
                : 18 June 2021
                : 11 August 2021
                : 16 August 2021
                Page count
                Figures: 5, Tables: 1, Pages: 11
                Custom metadata
                1
                research_paper

                Entomology,Parasitology,Ecology,Molecular biology,Pests, Diseases & Weeds
                EAG,Insecticide resistance,Pheromone binding proteins,Mating behavior,Wind tunnel

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