4.7 Article

Risk Assessment of Fluxametamide Resistance and Fitness Costs in Fall Armyworm (Spodoptera frugiperda)

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TOXICS
卷 11, 期 4, 页码 -

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MDPI
DOI: 10.3390/toxics11040307

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isoxazoline; fall armyworm; realized heritability; cross-resistance; detoxification enzyme; demography; life table

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This study aimed to evaluate the resistance risk of fall armyworm (FAW) to the insecticide fluxametamide and the associated fitness costs. Continuous exposure to fluxametamide did not result in an obvious increase in resistance in the FAW population after 10 generations of selection. The heritability of fluxametamide resistance was estimated as 0.084. Fluxametamide selection affected the development and reproductive traits of FAW, indicating a lower risk of resistance evolution.
The fall armyworm (FAW), Spodoptera frugiperda, is one of the most devastating invasive polyphagous pests, which has attracted recent global attention by developing resistance to various insecticidal active ingredients with independent mode of action. Fluxametamide, a newly commercialized isoxazoline insecticide, is exceptionally selective towards several lepidopteran pests. The present study aimed to evaluate resistance risk in FAW to fluxametamide and the fitness costs associated with fluxametamide resistance. A field-collected and genetically mixed population of FAW was artificially selected through continuous exposure to fluxametamide. After successive selection of 10 generations, there was no obvious increase in the LC50 (RF: 2.63-fold). The realized heritability (h(2)) of fluxametamide resistance was estimated as h(2) = 0.084 using a quantitative genetic approach. Compared with the susceptible F0 strain, the Flux-SEL (F10) strain of FAW displayed no significant cross-resistance to broflanilide, chlorantraniliprole, fipronil, indoxacarb, lambda cyhalothrin, spinetoram, and tetraniliprole, except emamectin benzoate (RF: 2.08-fold). Increased activity of glutathione S-transferase (ratio 1.94) was observed in the Flux-SEL (F10) strain of FAW, while the cytochrome P450 and carboxylesterase activities were not altered. The fluxametamide-selection significantly affected the development and reproductive traits of FAW with a lower R-0, T and relative fitness (R-f = 0.353). The results alluded that the risk of fluxametamide resistance evolution in FAW is relatively lower; however, proactive implementation of resistance management approaches should be done to maintain the field efficacy of fluxametamide against FAW.

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