Ecology and Evolutionary Biology, University of Colorado, Boulder, CO 80309, USA.
Ecol Lett. 2012 Mar;15(3):235-42. doi: 10.1111/j.1461-0248.2011.01730.x. Epub 2012 Jan 5.
Parasite infections often lead to dramatically different outcomes among host species. Although an emerging body of ecoimmunological research proposes that hosts experience a fundamental trade-off between pathogen defences and life-history activities, this line of inquiry has rarely been extended to the most essential outcomes of host-pathogen interactions: namely, infection and disease pathology. Using a comparative experimental approach involving 13 amphibian host species and a virulent parasite, we test the hypothesis that 'pace-of-life' predicts parasite infection and host pathology. Trematode exposure increased mortality and malformations in nine host species. After accounting for evolutionary history, species that developed quickly and metamorphosed smaller ('fast-species') were particularly prone to infection and pathology. This pattern likely resulted from both weaker host defences and greater adaptation by parasites to infect common hosts. Broader integration between life history theory and disease ecology can aid in identifying both reservoir hosts and species at risk of disease-driven declines.
寄生虫感染通常会导致宿主物种的结果产生显著差异。尽管越来越多的生态免疫学研究表明,宿主在病原体防御和生活史活动之间存在着根本的权衡,但这一研究方向很少扩展到宿主-病原体相互作用的最基本结果:即感染和疾病病理学。本研究采用涉及 13 种两栖宿主物种和一种毒性寄生虫的比较实验方法,检验了“生活节奏”预测寄生虫感染和宿主病理学的假说。吸虫暴露增加了 9 种宿主物种的死亡率和畸形率。在考虑了进化历史后,发育迅速且变态较小的“快速物种”(fast-species)特别容易受到感染和病理影响。这种模式可能是由于宿主防御能力较弱,以及寄生虫更适应感染常见宿主所致。将生活史理论和疾病生态学更广泛地结合起来,可以帮助识别储存宿主和面临疾病驱动下降风险的物种。