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首页> 外文期刊>Pest Management Science >Cross-resistance between cyenopyrafen and pyridaben in the twospotted spider mite Tetranychus urticae (Acari: Tetranychidae)
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Cross-resistance between cyenopyrafen and pyridaben in the twospotted spider mite Tetranychus urticae (Acari: Tetranychidae)

机译:在两个斑点的蜘蛛螨Tetranychus urticae(Acari:Tetranychidae)中的氰基吡喃芬和哒虫啉之间的交叉抗性。

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摘要

BACKGROUND: Cyenopyrafen is an inhibitor of complex II of the mitochondrial electron transport chain. It has a molecular structure that shares some common features with frequently used complex I inhibitors such as pyridaben. To evaluate whether this similarity in structure poses a cross-resistance riskthat might complicate resistance management, we selected for pyridaben and cyenopyrafen resistance in the laboratory and characterized resistance. RESULTS: The selection for cyenopyrafen conferred cross-resistance to pyridaben and vice versa. Resistance towards these both acaricides was incompletely dominant in adult females. However, in eggs maternal effects were observed in pyridaben resistance, but not in the cyenopyrafen-resistance (completely dominant). In the cyenopyrafen resistant strain, the LC_(50) of eggs remained lower than the commercially recommended concentration. The common detoxification mechanisms by cytochrome P450 was involved in resistance to these acaricides. Carboxyl esterases were also involved in cyenopyrafen resistance as a major factor. CONCLUSIONS: Although cross-resistance suggests that pyridaben resistance would confer cyenopyrafen cross-resistance, susceptibility in eggs functions to delay the development of cyenopyrafen resistance.
机译:背景:Cyenopyrafen是线粒体电子传输链复合物II的抑制剂。它的分子结构与常用的复杂I抑制剂(如哒嗪)具有某些共同特征。为了评估这种结构上的相似性是否会带来可能使耐药性管理变得复杂的交叉耐药性风险,我们在实验室中选择了哒哒苯醚和氰基吡喃类药物的耐药性,并表征了耐药性。结果:氰基吡喃的选择赋予了对哒巴啶交叉抗性,反之亦然。对这两种杀螨剂的抗性在成年雌性中不完全占优势。然而,在卵中观察到了对吡达本抗性的母体效应,但对苯并吡喃芬抗性却没有(完全占主导)。在对赛诺吡芬抗性的菌株中,卵的LC_(50)仍然低于商业推荐的浓度。细胞色素P450的常见排毒机制与对这些杀螨剂的抗性有关。羧酯酶也参与了对嘧嘧啶的抗性作为主要因素。结论:尽管交叉抗药性表明吡虫啉抗性会赋予cypynpyrafen交叉抗性,但是鸡蛋中的药敏作用会延迟cyenopyrafen抗性的发展。

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