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

细胞色素P450 药理学 生物 化学 生物化学
作者
Hong Zhou,Fenglin Wan,Xiangning Lai,Fangfang Yan,Miao Zhang,Yi Ni,Yutong Guo,Pan Zhang,Fuyou Guo,Matthana Klakong,Gen Peng,Wenhan Guo,Xinru Zeng,Zongjin Zhang,Xingbing Pan,Yu Liu,Liang Yang,Shili Li,Wei Ding
出处
期刊:Pest Management Science [Wiley]
卷期号:80 (10): 5035-5049 被引量:1
标识
DOI:10.1002/ps.8228
摘要

Abstract BACKGROUND Plants 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. RESULTS Scoparone 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 . CONCLUSIONS These 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.
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