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Pyrethroid synergists suppress esterase-mediated resistance in Indian strains of the cotton bollworm, Helicoverpa armigera (Hubner)

机译:拟除虫菊酯增效剂抑制印度棉铃虫Helicoverpa armigera(Hubner)品系中酯酶介导的抗性

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The role of esterase in pyrethroid resistance was studied in the final larval instar of different strains of the cotton bollworm, Helicoverpa armigera. The resistant strains viz., Nagpur strain and the Delhi strain were found to have elevated midgut esterase activity in comparison to the susceptible strain. Nagpur strain and Delhi strain have 2.24 and 1.73-fold higher esterase activity, respectively, than that of the susceptible strain. The Native PAGE displayed important differences in the midgut esterase isozyme pattern between the susceptible and the pyrethroid-resistant strains. Out of the 10 esterase isozyme observed, susceptible strain lacked three bands, E2, E6 and E10 that were found in the resistant strains. The potency of the synergists piperonyl butoxide (PBO) and dihydrodillapiole (DDA) as esterase inhibitor were also studied both in vitro and in vivo. The in vitro results clearly show that both PBO and DDA inhibited esterase activity in the two resistant strains, while there was almost no esterase inhibition in the homogenate of the susceptible strain. The in vivo inhibition studies (topical application of PBO and DDA followed by biochemical analysis) illustrated that PBO- and DDA-esterase binding is rather slow and non permanent process. Esterase inhibition did not occur immediately after the synergist treatment but at 4 and 8 h post treatment in case of PBO and DDA, respectively. Native PAGE revealed that the in vivo esterase inhibition caused by both PBO and DDA was due to the binding of the synergist with the E6 isozyme which was not present in the susceptible strain
机译:在棉铃虫Helicoverpa armigera不同菌株的最终幼虫期中研究了酯酶在拟除虫菊酯抗性中的作用。与易感菌株相比,发现抗性菌株,即Nagpur菌株和Delhi菌株具有提高的中肠酯酶活性。 Nagpur菌株和Delhi菌株的酯酶活性分别比易感菌株高2.24和1.73倍。天然PAGE在易感和拟除虫菊酯抗性菌株之间的中肠酯酶同工酶模式上显示出重要差异。在观察到的10种酯酶同工酶中,易感菌株缺少在抗性菌株中发现的三个条带E2,E6和E10。还在体内和体外研究了增效剂胡椒基丁醚(PBO)和二氢吡喃哌啶(DDA)作为酯酶抑制剂的效力。体外结果清楚地表明,PBO和DDA都抑制了这两种抗性菌株的酯酶活性,而在易感菌株的匀浆中几乎没有酯酶的抑制作用。体内抑制研究(局部应用PBO和DDA,然后进行生化分析)表明,PBO和DDA-酯酶的结合相当缓慢且非永久性。增效剂治疗后并未立即发生酯酶抑制作用,但分别在PBO和DDA的情况下在治疗后4和8 h发生。天然PAGE揭示PBO和DDA引起的体内酯酶抑制作用是由于增效剂与易感菌株中不存在的E6同工酶结合所致

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