Evolutionary Ecology Laboratory, Institute of Ecology and Evolution, University of Bern, Baltzerstrasse 6, Bern, Switzerland.
CNRS; Université de Lyon, F-69000, Lyon; Université Lyon 1; Department of Biometry and Evolutionary Biology, LBBE UMR 5558, Bâtiment Gregor Mendel, 43 boulevard du 11 novembre 1918, F-69622, Villeurbanne, France.
BMC Evol Biol. 2018 Jun 19;18(1):99. doi: 10.1186/s12862-018-1205-2.
In host-parasite systems, relative dispersal rates condition genetic novelty within populations and thus their adaptive potential. Knowledge of host and parasite dispersal rates can therefore help us to understand current interaction patterns in wild populations and why these patterns shift over time and space. For generalist parasites however, estimates of dispersal rates depend on both host range and the considered spatial scale. Here, we assess the relative contribution of these factors by studying the population genetic structure of a common avian ectoparasite, the hen flea Ceratophyllus gallinae, exploiting two hosts that are sympatric in our study population, the great tit Parus major and the collared flycatcher Ficedula albicollis. Previous experimental studies have indicated that the hen flea is both locally maladapted to great tit populations and composed of subpopulations specialized on the two host species, suggesting limited parasite dispersal in space and among hosts, and a potential interaction between these two structuring factors.
C. gallinae fleas were sampled from old nests of the two passerine species in three replicate wood patches and were genotyped at microsatellite markers to assess population genetic structure at different scales (among individuals within a nest, among nests and between host species within a patch and among patches). As expected, significant structure was found at all spatial scales and between host species, supporting the hypothesis of limited dispersal in this parasite. Clustering analyses and estimates of relatedness further suggested that inbreeding regularly occurs within nests. Patterns of isolation by distance within wood patches indicated that flea dispersal likely occurs in a stepwise manner among neighboring nests. From these data, we estimated that gene flow in the hen flea is approximately half that previously described for its great tit hosts.
Our results fall in line with predictions based on observed patterns of adaptation in this host-parasite system, suggesting that parasite dispersal is limited and impacts its adaptive potential with respect to its hosts. More generally, this study sheds light on the complex interaction between parasite gene flow, local adaptation and host specialization within a single host-parasite system.
在宿主-寄生虫系统中,相对扩散率决定了种群内的遗传新颖性,从而决定了它们的适应潜力。因此,了解宿主和寄生虫的扩散率可以帮助我们理解野生种群中当前的相互作用模式,以及这些模式为何随时间和空间而变化。然而,对于广宿主寄生虫来说,扩散率的估计取决于宿主范围和所考虑的空间尺度。在这里,我们通过研究一种常见的鸟类外寄生虫——鸡蚤(Ceratophyllus gallinae)的种群遗传结构,来评估这些因素的相对贡献,该寄生虫在我们的研究种群中与两种共生的宿主——大山雀(Parus major)和白喉唐纳雀(Ficedula albicollis)有关。先前的实验研究表明,鸡蚤在本地对大山雀种群适应不良,并且由专门针对两种宿主物种的亚种群组成,这表明寄生虫在空间和宿主之间的扩散受到限制,并且存在这两个结构因素之间的潜在相互作用。
从两种雀形目鸟类的旧巢中采集鸡蚤样本,并在三个重复的树林斑块中使用微卫星标记进行基因分型,以评估不同尺度(巢内个体之间、巢之间、斑块内宿主种间以及斑块间)的种群遗传结构。正如预期的那样,在所有空间尺度和宿主种间都发现了显著的结构,支持了寄生虫扩散受限的假设。聚类分析和相关性估计进一步表明,在巢内经常发生近亲繁殖。树林斑块内的隔离与距离模式表明,鸡蚤的扩散可能是在相邻巢之间逐步进行的。根据这些数据,我们估计鸡蚤的基因流大约是其大山雀宿主先前描述的一半。
我们的结果符合基于该宿主-寄生虫系统中观察到的适应模式的预测,表明寄生虫的扩散受到限制,并对其相对于宿主的适应潜力产生影响。更一般地说,这项研究揭示了单一宿主-寄生虫系统中寄生虫基因流、本地适应和宿主专化之间复杂的相互作用。