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发现选择性乙酰胆碱酯酶抑制剂以控制(蜱螨目:叶螨科)。

Discovery selective acetylcholinesterase inhibitors to control Tetranychus urticae (Acari: Tetranychidae).

机构信息

Key Laboratory of Northern Urban Agriculture of Ministry of Agriculture and Rural Affairs, College of Bioscience and Resource Environment, Beijing University of Agriculture, Beijing 102206, China.

Center for Growth, Metabolism and Aging, Key Laboratory of Bio-Resources and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu 610064, China.

出版信息

J Insect Sci. 2023 Jul 1;23(4). doi: 10.1093/jisesa/iead073.

Abstract

The two-spotted spider mite, Tetranychus urticae Koch, has a broad host plant range and presents an extreme capacity for developing pesticide resistance, becoming a major economic pest in agriculture. Anticholinesterase insecticides still account for a big part of global insecticide sales. However, there is a growing concern about the serious resistance problems of anticholinesterase insecticides and their nontarget toxicity. In this study, structure-based virtual screening was performed to discover selective AChE inhibitors from the ChemBridge database, and 39 potential species-specific AChE inhibitor were obtained targeting T. urticae AChE, but not human AChE. Among them, compound No. 8 inhibited AChE from T. urticae, but not from human, and had an inhibitory activity comparable to that of eserine. Compound No. 8 had dose-dependent toxicity to T. urticae in glass slide-dipping assay and had significant mite control effects in a pot experiment, but required a high concentration to achieve similar control effects to spirodiclofen. The toxicity evaluation suggested that compound No. 8 had no acute toxicity on pollinator honey bees and natural predator N. californicus and did not affect strawberry growth in our assay. Compound No. 8 is a potential lead compound for developing novel acaricides with reduced nontarget toxicity.

摘要

二斑叶螨,Tetranychus urticae Koch,拥有广泛的宿主植物范围,并具有极强的抗药性发展能力,成为农业中的主要经济害虫。乙酰胆碱酯酶抑制剂杀虫剂仍占全球杀虫剂销售额的很大一部分。然而,人们越来越关注乙酰胆碱酯酶抑制剂的严重抗药性问题及其非靶标毒性。在这项研究中,我们进行了基于结构的虚拟筛选,以从 ChemBridge 数据库中发现对 Tetranychus urticae AChE 具有选择性的 AChE 抑制剂,共获得 39 种针对 Tetranychus urticae AChE 的潜在种特异性 AChE 抑制剂,但对人 AChE 没有抑制作用。其中,化合物 8 抑制了来自二斑叶螨的 AChE,但对人 AChE 没有抑制作用,其抑制活性可与 eserine 相媲美。化合物 8 在玻璃载玻片浸渍试验中对二斑叶螨具有剂量依赖性毒性,并在盆栽试验中对螨虫具有显著的防治效果,但需要高浓度才能达到与螺螨酯相似的防治效果。毒性评价表明,化合物 8 对传粉蜂和自然捕食者 N. californicus 没有急性毒性,在我们的试验中也不会影响草莓的生长。化合物 8 是开发具有降低非靶标毒性的新型杀螨剂的潜在先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c78/10424716/064e1ca46394/iead073_fig1.jpg

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