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保护蜜蜂:通过计算机模拟、体外和体内研究鉴定一种新型杀螨剂。

Protecting honey bees: identification of a new varroacide by in silico, in vitro, and in vivo studies.

作者信息

Dulin Fabienne, Zatylny-Gaudin Céline, Ballandonne Céline, Guillet Bertrand, Bonafos Romain, Bureau Ronan, Halm Marie Pierre

机构信息

University of Caen Basse-Normandie, Caen, France,

出版信息

Parasitol Res. 2014 Dec;113(12):4601-10. doi: 10.1007/s00436-014-4150-z. Epub 2014 Oct 31.

Abstract

Varroa destructor is the main concern related to the gradual decline of honeybees. Nowadays, among the various acaricides used in the control of V. destructor, most presents increasing resistance. An interesting alternative could be the identification of existent molecules as new acaricides with no effect on honeybee health. We have previously constructed the first 3D model of AChE for honeybee. By analyzing data concerning amino acid mutations implicated in the resistance associated to pesticides, it appears that pirimicarb should be a good candidate for varroacide. To check this hypothesis, we characterized the AChE gene of V. destructor. In the same way, we proposed a 3D model for the AChE of V. destructor. Starting from the definition of these two 3D models of AChE in honeybee and varroa, a comparison between the gorges of the active site highlighted some major differences and particularly different shapes. Following this result, docking studies have shown that pirimicarb adopts two distinct positions with the strongest intermolecular interactions with VdAChE. This result was confirmed with in vitro and in vivo data for which a clear inhibition of VdAChE by pirimicarb at 10 μM (contrary to HbAChE) and a 100% mortality of varroa (dose corresponding to the LD50 (contact) for honeybee divided by a factor 100) were observed. These results demonstrate that primicarb could be a new varroacide candidate and reinforce the high relationships between in silico, in vitro, and in vivo data for the design of new selective pesticides.

摘要

狄氏瓦螨是与蜜蜂数量逐渐减少相关的主要问题。如今,在用于防治狄氏瓦螨的各种杀螨剂中,大多数都出现了越来越强的抗性。一个有趣的替代方法可能是鉴定现有的分子作为对蜜蜂健康无影响的新型杀螨剂。我们之前构建了蜜蜂乙酰胆碱酯酶(AChE)的首个三维模型。通过分析与农药抗性相关的氨基酸突变数据,看来抗蚜威应该是杀螨剂的一个良好候选物。为了验证这一假设,我们对狄氏瓦螨的AChE基因进行了表征。同样,我们提出了狄氏瓦螨AChE的三维模型。从蜜蜂和狄氏瓦螨这两种AChE三维模型的定义出发,活性位点峡谷之间的比较突出了一些主要差异,尤其是不同的形状。基于这一结果,对接研究表明抗蚜威在与狄氏瓦螨乙酰胆碱酯酶(VdAChE)的相互作用中采取了两个不同的位置,具有最强的分子间相互作用。这一结果得到了体外和体内数据的证实,在这些数据中观察到10 μM的抗蚜威对VdAChE有明显抑制作用(与蜜蜂乙酰胆碱酯酶(HbAChE)相反),并且狄氏瓦螨有100%的死亡率(剂量相当于蜜蜂经接触途径的半数致死剂量(LD50)除以100)。这些结果表明抗蚜威可能是一种新型杀螨剂候选物,并加强了计算机模拟、体外和体内数据在新型选择性农药设计中的高度相关性。

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