Tao Leiling, Hoang Kevin M, Hunter Mark D, de Roode Jacobus C
Department of Biology, Emory University, 1510 Clifton Road, Atlanta, GA, 30322, USA.
Department of Ecology and Evolutionary Biology, University of Michigan, 830 N University Avenue, Ann Arbor, MI, 48109, USA.
J Anim Ecol. 2016 Sep;85(5):1246-54. doi: 10.1111/1365-2656.12558. Epub 2016 Jul 21.
The emerging field of ecological immunology demonstrates that allocation by hosts to immune defence against parasites is constrained by the costs of those defences. However, the costs of non-immunological defences, which are important alternatives to canonical immune systems, are less well characterized. Estimating such costs is essential for our understanding of the ecology and evolution of alternative host defence strategies. Many animals have evolved medication behaviours, whereby they use antiparasitic compounds from their environment to protect themselves or their kin from parasitism. Documenting the costs of medication behaviours is complicated by natural variation in the medicinal components of diets and their covariance with other dietary components, such as macronutrients. In the current study, we explore the costs of the usage of antiparasitic compounds in monarch butterflies (Danaus plexippus), using natural variation in concentrations of antiparasitic compounds among plants. Upon infection by their specialist protozoan parasite Ophryocystis elektroscirrha, monarch butterflies can selectively oviposit on milkweed with high foliar concentrations of cardenolides, secondary chemicals that reduce parasite growth. Here, we show that these antiparasitic cardenolides can also impose significant costs on both uninfected and infected butterflies. Among eight milkweed species that vary substantially in their foliar cardenolide concentration and composition, we observed the opposing effects of cardenolides on monarch fitness traits. While high foliar cardenolide concentrations increased the tolerance of monarch butterflies to infection, they reduced the survival rate of caterpillars to adulthood. Additionally, although non-polar cardenolide compounds decreased the spore load of infected butterflies, they also reduced the life span of uninfected butterflies, resulting in a hump-shaped curve between cardenolide non-polarity and the life span of infected butterflies. Overall, our results suggest that the use of antiparasitic compounds carries substantial costs, which could constrain host investment in medication behaviours.
新兴的生态免疫学领域表明,宿主用于抵御寄生虫的免疫防御资源分配受到这些防御成本的限制。然而,作为传统免疫系统重要替代的非免疫防御成本,其特征尚不明确。估算此类成本对于我们理解替代宿主防御策略的生态学和进化至关重要。许多动物进化出了用药行为,即它们利用环境中的抗寄生虫化合物来保护自己或亲属免受寄生虫侵害。饮食中药物成分的自然变异及其与其他饮食成分(如大量营养素)的协方差,使得记录用药行为的成本变得复杂。在当前的研究中,我们利用植物中抗寄生虫化合物浓度的自然变异,探索帝王蝶(黑脉金斑蝶)使用抗寄生虫化合物的成本。受到其专性原生动物寄生虫微孢子虫感染后,帝王蝶能够选择性地在叶片中强心甾含量高的马利筋上产卵,强心甾是一种能抑制寄生虫生长的次生化学物质。在这里,我们表明这些抗寄生虫强心甾也会给未感染和已感染的蝴蝶带来显著成本。在八种叶片强心甾浓度和成分差异很大的马利筋物种中,我们观察到了强心甾对帝王蝶适合度性状的相反影响。虽然叶片强心甾浓度高会提高帝王蝶对感染的耐受性,但会降低毛虫到成年期的存活率。此外,尽管非极性强心甾化合物降低了已感染蝴蝶的孢子负荷,但也缩短了未感染蝴蝶的寿命,导致强心甾非极性与已感染蝴蝶寿命之间呈驼峰状曲线。总体而言,我们的结果表明,使用抗寄生虫化合物会带来巨大成本,这可能会限制宿主在用药行为上的投入。