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首页> 外文期刊>Pesticide Biochemistry and Physiology >Identification of resistance-responsive proteins in larvae of Bactrocera dorsalis (Hendel), for pyrethroid toxicity by a proteomic approach
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Identification of resistance-responsive proteins in larvae of Bactrocera dorsalis (Hendel), for pyrethroid toxicity by a proteomic approach

机译:通过蛋白质组学方法鉴定背果小实蝇(Hendel)幼虫中的抗药性蛋白对拟除虫菊酯的毒性

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Insect resistance to the pyrethroid toxins has been examined previously using a number of traditional biochemical and molecular techniques. In this study, a proteomic approach involving two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) and tandem mass spectrometry (MS/MS) were applied to examine changes in resistant stains larvae of Bactracera dorsalis Hendel induced by pyrethroid treatment over a 3 h, 6 h and 12 h time period, and a number of proteins changes were observed to change in the level of regulation. Out of total 15 proteins, 9 proteins were observed only after pyrethroid treatment; 6 proteins showed different expression. After MALDI-TOF analyses and peptide mapping method, the data was compared with those of the known proteins available in public databases. Sequence analyses revealed that resistance response correlates with up-regulation (glycerol-3-phosphate dehydrogenase) and down-regulation (ATPADP antiporter) of energy-related proteins. It indicated that increased metabolism and energy-indeed as a resistance response to pyrethroid toxins. The regulation of cytoskeleton proteins were possibly a B. dorsalis tissue repair response or in cell division. Up-regulation of protein synthesis would results in substantial bioenergetic enhancement, suggesting a trade-off insect resistance to pyrethroid. Down regulation of neural protein indicated that neural system was physically injured after pyrethroid stress. Some remaining proteins were not identifiable, suggesting these may be novel proteins. Oriental fruit fly proteomes of pesticide induced provide an integrative basis for consolidating our knowledge of insect resistance. The results pave the way for future investigation of the alteration of the insect resistance to chemical pesticides.
机译:以前已经使用许多传统的生化和分子技术检查了昆虫对拟除虫菊酯毒素的抗性。在这项研究中,蛋白质组学方法涉及二维聚丙烯酰胺凝胶电泳(2D-PAGE),基质辅助激光解吸/电离飞行时间(MALDI-TOF)和串联质谱(MS / MS)拟除虫菊酯处理在3 h,6 h和12 h时间段内诱导的反实蝇(Bactracera dorsalis Hendel)幼虫的抗污渍变化,并且观察到许多蛋白质变化会影响调节水平。在总共15种蛋白质中,仅在拟除虫菊酯处理后才观察到9种蛋白质。 6种蛋白质表现出不同的表达。经过MALDI-TOF分析和肽图分析方法后,将数据与公共数据库中可用的已知蛋白质进行了比较。序列分析表明,抗性反应与能量相关蛋白的上调(甘油3-磷酸脱氢酶)和下调(ATPADP反转运蛋白)相关。这表明新陈代谢的增加和能量的确是对拟除虫菊酯毒素的抗性反应。细胞骨架蛋白的调节可能是背侧双歧杆菌的组织修复反应或细胞分裂。蛋白质合成的上调将导致生物能的显着增强,表明昆虫对拟除虫菊酯具有抗性。神经蛋白的下调表明拟除虫菊酯胁迫后神经系统受到了物理损伤。一些剩余的蛋白质无法鉴定,表明它们可能是新颖的蛋白质。农药诱导的东方果蝇蛋白质组学为巩固我们的抗虫性知识提供了综合基础。该结果为进一步研究昆虫对化学农药的抗性变化铺平了道路。

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