Centre for Immunity, Infection, and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh, UK.
Evolution. 2011 Nov;65(11):3298-310. doi: 10.1111/j.1558-5646.2011.01382.x. Epub 2011 Jul 21.
Within- and between-host disease processes occur on the same timescales, therefore changes in the within-host dynamics of parasites, resources, and immunity can interact with changes in the epidemiological dynamics to affect evolutionary outcomes. Consequently, studies of the evolution of disease life histories, that is, infection-age-specific patterns of transmission and virulence, have been constrained by the need for a mechanistic understanding of within-host disease dynamics. In a companion paper (Day et al. 2011), we develop a novel approach that quantifies the relevant within-host aspects of disease through genetic covariance functions. Here, we demonstrate how to apply this theory to data. Using two previously published datasets from rodent malaria infections, we show how to translate experimental measures into disease life-history traits, and how to quantify the covariance in these traits. Our results show how patterns of covariance can interact with epidemiological dynamics to affect evolutionary predictions for disease life history. We also find that the selective constraints on disease life-history evolution can vary qualitatively, and that "simple" virulence-transmission trade-offs that are often the subject of experimental investigation can be obscured by trade-offs within one trait alone. Finally, we highlight the type and quality of data required for future applications.
在宿主内和宿主间的疾病过程发生在同一时间尺度上,因此寄生虫、资源和免疫的宿主内动态变化可以与流行病学动态变化相互作用,从而影响进化结果。因此,对疾病生活史进化的研究,即感染年龄特异性的传播和毒力模式,受到了对宿主内疾病动态学的机制理解的限制。在一篇配套的论文中(Day 等人,2011 年),我们开发了一种新的方法,通过遗传协方差函数来量化疾病的相关宿主内方面。在这里,我们展示如何将这一理论应用于数据。利用来自啮齿动物疟疾感染的两个先前发表的数据集,我们展示了如何将实验测量转化为疾病生活史特征,以及如何量化这些特征之间的协方差。我们的结果表明,协方差模式如何与流行病学动态相互作用,从而影响疾病生活史的进化预测。我们还发现,疾病生活史进化的选择约束可以在质量上有所不同,并且通常是实验研究主题的“简单”毒力-传播权衡可能会被单一特征内的权衡所掩盖。最后,我们强调了未来应用所需的数据类型和质量。