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用于测定毒液和毒素口服杀虫活性的双翅目毒性试验。

Dipteran toxicity assays for determining the oral insecticidal activity of venoms and toxins.

作者信息

Guo Shaodong, Herzig Volker, King Glenn F

机构信息

Institute for Molecular Bioscience, The University of Queensland, St. Lucia QLD 4072, Australia.

Institute for Molecular Bioscience, The University of Queensland, St. Lucia QLD 4072, Australia.

出版信息

Toxicon. 2018 Aug;150:297-303. doi: 10.1016/j.toxicon.2018.06.077. Epub 2018 Jun 18.

DOI:10.1016/j.toxicon.2018.06.077
PMID:29920256
Abstract

The growing world population is placing an increasing demand on food production. In addition, abuse and misuse of chemical insecticides has led to the evolution of resistance in insect pests as well as environmental damage. Together, these developments have created a demand for new insecticidal compounds to facilitate global food production. Arachnid venom peptides provide an environmentally-friendly alternative as potential bioinsecticides given their advantages of being fully biodegradable, highly potent, and phyletically selective. However, the use of arachnid venom peptides as bioinsecticides has been questioned due to their presumed lack of oral toxicity. Thus, the aim of this work was to develop screens for oral insecticidal activity. Based on the high susceptibility of dipterans to venom peptides, fruit flies (Drosophila melanogaster) and sheep blowflies (Lucilia cuprina) were selected for screening 56 arachnid venoms. 71.4% of these venoms caused 50% or higher mortality in Drosophila, whereas 30.4% were lethal to blowflies at oral doses of 1 or 30 μg/fly, respectively. We used these assays to compare the oral and injection activity of four well-known spider venom peptides (Hv1a, Hv1c, Dc1a and Ta1a). Hv1c and Ta1a only showed weak or no oral activity in both species, while Hv1a and Dc1a showed higher oral activity in blowflies than Drosophila. Overall, we have established screens for oral toxicity in two dipteran insects. Our results indicate that oral insecticidal activity is more widespread in arachnid venoms than expected, and that some arachnid venoms and venom peptides exhibit phyletic differences in oral toxicity.

摘要

不断增长的世界人口对粮食生产的需求日益增加。此外,化学杀虫剂的滥用和误用导致害虫产生抗药性以及环境破坏。这些发展共同催生了对新型杀虫化合物的需求,以促进全球粮食生产。蛛形纲动物毒液肽作为潜在的生物杀虫剂,具有完全可生物降解、高效且具有系统发育选择性的优点,提供了一种环境友好的替代品。然而,由于推测蛛形纲动物毒液肽缺乏口服毒性,其作为生物杀虫剂的应用受到了质疑。因此,这项工作的目的是开发口服杀虫活性的筛选方法。基于双翅目昆虫对毒液肽的高度敏感性,选择果蝇(黑腹果蝇)和羊绿蝇(铜绿蝇)来筛选56种蛛形纲动物毒液。这些毒液中有71.4%在果蝇中导致50%或更高的死亡率,而分别以1或30μg/只的口服剂量对绿蝇有致死作用的毒液占30.4%。我们使用这些试验来比较四种著名的蜘蛛毒液肽(Hv1a、Hv1c、Dc1a和Ta1a)的口服和注射活性。Hv1c和Ta1a在这两个物种中仅表现出微弱的口服活性或无口服活性,而Hv1a和Dc1a在绿蝇中的口服活性高于果蝇。总体而言,我们已经建立了两种双翅目昆虫口服毒性的筛选方法。我们的结果表明,蛛形纲动物毒液中的口服杀虫活性比预期的更为普遍,并且一些蛛形纲动物毒液和毒液肽在口服毒性方面表现出系统发育差异。

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