Synergistic action and mechanism of scoparone, a key bioactive component of Artemisia capillaris, and spirodiclofen against spider mites

Author:

Zhou Hong1,Wan Fenglin1,Lai Xiangning1,Yan Fangfang2,Zhang Miao1,Ni Yi1,Guo Yutong1,Zhang Pan3,Guo Fuyou1,Klakong Matthana1,Peng Gen1,Guo Wenhan1,Zeng Xinru1,Zhang Zongjin2,Pan Xingbing2,Liu Yu2,Yang Liang1,Li Shili1,Ding Wei1ORCID

Affiliation:

1. Institute of Pesticide Science, College of Plant Protection, Southwest University Chongqing China

2. Panzhihua City Company, Sichuan Tobacco Company, China National Tobacco Corporation Panzhihua China

3. Key Laboratory of Molecular Genetics, Guizhou Institute of Tobacco Science, China National Tobacco Corporation Guiyang China

Abstract

AbstractBACKGROUNDPlants have numerous defensive secondary metabolites to withstand insect attacks. Scoparone, which is extracted from the medicinal plant Artemisia capillaris, has potent acaricidal effects on Tetranychus cinnabarinus. Spirodiclofen, derived from a tetronic acid derivative, is a potent commercial acaricide that is extensively used globally. However, whether scoparone has synergistic effects when used in conjunction with spirodiclofen and the underlying synergistic mechanism remains unclear.RESULTSScoparone exhibited a potent synergistic effect when it was combined with spirodiclofen at a 1:9 ratio. Subsequently, cytochrome P450 monooxygenase (P450) activity, RNA‐Seq and qPCR assays indicated that the enzyme activity of P450 and the expression of one P450 gene from T. cinnabarinus, TcCYP388A1, were significantly inhibited by scoparone and spirodiclofen + scoparone; conversely, P450 was activated in spirodiclofen‐exposed mites. Importantly, RNAi‐mediated silencing of the TcCYP388A1 gene markedly increased the susceptibility of spider mites to spirodiclofen, scoparone and spirodiclofen + scoparone, and in vitro, the recombinant TcCYP388A1 protein could metabolize spirodiclofen. Molecular docking and functional analyses further indicated that R117, which is highly conserved in Arachnoidea species, may be a vital specific binding site for scoparone in the mite TcCYP388A1 protein. This binding site was subsequently confirmed using mutagenesis data, which revealed that this binding site was the sole site selected by scoparone in spider mites over mammalian or fly CYP388A1.CONCLUSIONSThese results indicate that the synergistic effects of scoparone and spirodiclofen on mites occurs through the inhibition of P450 activity, thus reducing spirodiclofen metabolism. The synergistic effect of this potent natural product on the detoxification enzyme‐targeted activity of commercial acaricides may offer a sustainable strategy for pest mite resistance management. © 2024 Society of Chemical Industry.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Chongqing Postdoctoral Science Foundation

Publisher

Wiley

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