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青蒿素关键生物活性成分茵陈蒿素与螺螨酯协同作用及其对红蜘蛛的作用机制。

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

机构信息

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

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

出版信息

Pest Manag Sci. 2024 Oct;80(10):5035-5049. doi: 10.1002/ps.8228. Epub 2024 Jun 7.

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.

摘要

背景

植物拥有众多防御性次生代谢产物以抵御昆虫的侵害。从药用植物青蒿中提取的樟脑具有强烈的杀螨作用,可有效防治朱砂叶螨。螺螨酯来源于四氢呋喃酸衍生物,是一种广泛应用于全球的高效商业杀螨剂。然而,樟脑与螺螨酯联合使用时是否具有协同作用,以及潜在的协同作用机制尚不清楚。

结果

当樟脑与螺螨酯以 1:9 的比例联合使用时,表现出很强的协同作用。随后,细胞色素 P450 单加氧酶(P450)活性、RNA-Seq 和 qPCR 检测表明,P450 酶活性和朱砂叶螨中一个 P450 基因 TcCYP388A1 的表达均被樟脑和螺螨酯+樟脑显著抑制;相反,P450 在暴露于螺螨酯的螨中被激活。重要的是,通过 RNAi 介导的 TcCYP388A1 基因沉默显著增加了朱砂叶螨对螺螨酯、樟脑和螺螨酯+樟脑的敏感性,并且在体外,重组 TcCYP388A1 蛋白可以代谢螺螨酯。分子对接和功能分析进一步表明,在蛛形纲物种中高度保守的 R117 可能是该螨 TcCYP388A1 蛋白中樟脑的一个重要的特定结合位点。随后,通过突变数据证实了该结合位点的存在,结果表明,在朱砂叶螨中,该结合位点是樟脑在哺乳动物或果蝇 CYP388A1 中唯一选择的位点。

结论

这些结果表明,樟脑和螺螨酯对螨类的协同作用是通过抑制 P450 活性来实现的,从而降低了螺螨酯的代谢。这种高效天然产物对商业杀螨剂解毒酶靶向活性的协同作用可能为防治害虫螨提供一种可持续的策略。© 2024 化学工业协会。

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