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In vitro metabolism of pyriproxyfen by the housefly larvae

机译:鸟叶幼虫的吡匹昔斯杂草的体外代谢

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Housefly collected from the 3rd Yumenoshima dumping-island (YS strain) in Tokyo Bay of Japan developed 4,900-fold resistance from only 3.8-fold in the 3rd instar larvae to a juvenile hormone analog, pyriproxyfen, after laboratory selection with this chemical. The selected strain was thus named YPPF strain. Linkage group analysis of pyriproxyfen resistance revealed that resistance to this chemical in YPPF strain was multifactorial, with the most important factor being located on the 2nd chromosome. Toxicity bioassays of pyriproxyfen with synergists showed that the resistance of houseflies was depressed to 29-fold from 400-fold in white pupae by a ytochrome P450 inhibitor, 2-propynyl 2,3,6-trichlorophenyl ehter (PTPE). It is obvious that cytochrome P450 monooxygenase plays an important role in housefly resistance to pyriproxyfen.
机译:在日本东京湾的第三次玉树倾卸岛(ys菌株)收集的家蝇在第3次龄幼虫中仅开发了4,900倍的抗性,以少年激素类似物,吡吡咯烷蛋白,用这种化学品选择。 因此,所选择的菌株命名为YPPF菌株。 吡吡吡芬抗性的连杆组分析显示,在YPPF菌株中对该化学品的抗性是多重的,具有最重要的因素位于第二染色体上。 用Synergists的吡吡咯烷盐的毒性生物测定表明,通过YtOchrome P450抑制剂,2-丙炔基2,3,6-三氯苯基ε(PTPE),储质血管的抗性从400倍的白色蛹抑制至29倍。 很明显,细胞色素P450单氧化酶在杂草抗性对吡匹昔昔的抗性中起重要作用。

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