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Un-nesting DNA Russian dolls - the potential for constructing food webs using residual DNA in empty aphid mummies

机译:脱巢的DNA俄罗斯玩偶-在空的蚜虫木乃伊中利用残留的DNA构建食物网的潜力

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Constructing food-web assemblages comprising parasitoid wasps involves large field collections of hosts followed by labour-intensive rearing of the insects to evaluate the rates of parasitism along with morphological or molecular identification of the parasitoid species. This article presents research towards a new molecular method for the practical and accurate construction of aphid-based food webs. We hypothesize that parasitoid and hyperparasitoid DNA left inside aphid mummies after emergence of these third and fourth trophic-level guilds can be simultaneously detected using universal polymerase chain reaction (PCR) primers for nonspecific DNA amplification in combination with single-stranded conformation polymorphism (SSCP) analysis. Such a protocol theoretically allows food-web construction to be performed with no a priori knowledge of the species present. Moreover, the use of empty mummies circumvents rearing and minimizes labour and time in the field and laboratory. To test our hypothesis, we conducted DNA analyses on laboratory-produced parasitized aphids (mummies) from Myzus persicae and Brevicoryne brassicae (two important aphid pest species) after exposure to the parasitoid Diaeretiella rapae and the hyperparasitoid Asaphes vulgaris. DNA is amplifiable in empty aphid mummies for as long as 3 weeks after parasitoid emergence. However, the simultaneous identification of several species in a single mummy sample was rare, which hinders the accurate inference of trophic links. DNA quality and relative quantity, together with preferential amplification, are potential explanations of current results. Technical refinements are needed to ensure full reliability and detection of complex trophic links. The use of PCR-SSCP for foodweb construction is novel, and its potential to include an important number of different species is yet to be fully explored.
机译:构建包括寄生蜂的食物网组合涉及宿主的大田地收集,随后是劳动强度大的昆虫饲养,以评估寄生虫的发生率以及寄生虫的形态或分子鉴定。本文介绍了一种新的分子方法的研究,以实用,准确地构建基于蚜虫的食物网。我们假设,使用通用聚合酶链反应(PCR)引物结合单链构象多态性(SSCP)可以同时检测非特异DNA扩增同时检测到蚜虫木乃伊中残留在蚜虫木乃伊中的寄生虫和超寄生虫DNA。分析。这样的协议理论上允许在没有先验知识的情况下进行食物网的构建。此外,使用空的木乃伊可以避免饲养,并最大程度地减少了现场和实验室的劳动和时间。为了检验我们的假设,我们在暴露于寄生性菜蛾Diaeretiella rapae和超寄生性菜豆Asaphes vulgaris之后,对了实验室生产的桃蚜和两个小蚜虫Brevicoryne Brasicae的寄生蚜虫(木乃伊)进行了DNA分析。在寄生蚜虫出现后长达3周的时间里,DNA在空的蚜虫木乃伊中均可扩增。然而,在单个木乃伊样品中同时鉴定几种物种的情况很少见,这妨碍了对营养连接的准确推断。 DNA的质量和相对数量,以及优先的扩增,是目前结果的潜在解释。需要进行技术改进以确保完全的可靠性和复杂的营养链接的检测。 PCR-SSCP在食物网构建中的应用是新颖的,其潜力包括许多不同物种尚未得到充分探索。

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