4.7 Article

Toxicological and molecular profiling of insecticide resistance in a Brazilian strain of fall armyworm resistant to Bt Cry1 proteins

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PEST MANAGEMENT SCIENCE
卷 77, 期 8, 页码 3713-3726

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JOHN WILEY & SONS LTD
DOI: 10.1002/ps.6061

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fall armyworm; cross-resistance; detoxification enzymes; resistance management

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The study found that the Bt-resistant Brazilian strain Sf_Des has medium resistance to deltamethrin and chlorpyrifos, high cross-resistance to Cry1 toxins but high susceptibility to Vip3A. In comparison to the susceptible strain Sf_Bra, Sf_Des exhibited up to 19-fold increased cytochrome P450 activity and upregulation of multiple P450 transcripts. Gene Ontology analysis categorized most differentially expressed genes into oxidation-reduction and metabolic processes.
Background Spodoptera frugiperda, fall armyworm (FAW) is the major pest of maize in Brazil and has readily acquired field resistance to a broad range of synthetic insecticides and toBacillus thuringiensis(Bt) insecticidal proteins expressed in important crops. This study aims to understand patterns of cross-resistance in FAW by investigating the toxicological profile of a Bt-resistant Brazilian strain (Sf_Des) in comparison to a Bt-susceptible strain (Sf_Bra). Results Laboratory bioassays with 15 active substances of nine mode of action classes revealed that Sf_Des has a medium level of resistance to deltamethrin and chlorpyrifos. Very high cross-resistance was observed among Cry1 toxins, but high susceptibility against Vip3A. Strain Sf_Des exhibited - depending on the substrate - up to 19-fold increased cytochrome P450 activity in comparison to Sf_Bra. RNA-Seq data support a major role of P450 enzymes in the detoxification of insecticides because we detected 85 P450 transcripts upregulated in Sf_Des. Quantitative reverse transcription polymerase chain reaction (RT-qPCR) analysis confirmed thatCYP9A-like andCYP6B39are significantly upregulated (>200-fold) in Sf_Des in comparison to Sf_Bra strain. No target-site mutation linked to pyrethroid resistance was detected, but mutations in the AChE linked to organophosphate resistance were observed in Sf_Des. A Gene Ontology (GO) analysis of differentially expressed genes (DEG) categorized most of them into the biological process category, involved in oxidation-reduction and metabolic processes. Conclusion Our results indicate that multiple/cross-resistance mechanisms may have developed in the Sf_Des strain to conventional insecticides and Bt insecticidal proteins. The systematic toxicological analysis presented will help to guide recommendations for an efficient resistance management.

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