Bio-Protection Research Centre, Lincoln University, PO Box 85084, Lincoln, 7647, New Zealand.
Mol Ecol. 2014 Aug;23(15):3925-33. doi: 10.1111/mec.12633. Epub 2014 Jan 22.
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 food-web construction is novel, and its potential to include an important number of different species is yet to be fully explored.
构建包含寄生蜂的食物网组合涉及大量宿主的野外采集,然后需要进行劳动密集型的昆虫饲养,以评估寄生率,并对寄生蜂物种进行形态或分子鉴定。本文介绍了一种新的分子方法,用于实际和准确地构建基于蚜虫的食物网。我们假设,在第三和第四营养级 guild 的蚜虫成虫后,留在蚜虫木乃伊内部的寄生蜂和重寄生蜂 DNA 可以使用通用聚合酶链反应 (PCR) 引物同时检测,这些引物用于非特异性 DNA 扩增,并结合单链构象多态性 (SSCP) 分析。这种方案理论上允许在没有关于存在物种的先验知识的情况下进行食物网构建。此外,使用空木乃伊可以避免饲养,并最大限度地减少野外和实验室的劳动力和时间。为了验证我们的假设,我们对实验室生产的被寄生的蚜虫(木乃伊)进行了 DNA 分析,这些蚜虫来自桃蚜和小菜蛾(两种重要的蚜虫害虫),暴露于寄生蜂小菜蛾多胚跳小蜂和重寄生蜂普通菜蚜茧蜂之后。在寄生蜂出现后长达 3 周的时间内,空蚜虫木乃伊中的 DNA 是可扩增的。然而,在单个木乃伊样本中同时鉴定出几种物种的情况很少见,这阻碍了对营养联系的准确推断。DNA 质量和相对数量,以及优先扩增,是当前结果的潜在解释。需要技术改进以确保充分的可靠性和复杂营养联系的检测。PCR-SSCP 用于食物网构建是新颖的,其包含大量不同物种的潜力尚未得到充分探索。