Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.
Department of Biology, University of Utah, Salt Lake City, UT, USA.
J Anim Ecol. 2018 Mar;87(2):323-330. doi: 10.1111/1365-2656.12692. Epub 2017 Jun 26.
Gut microbial communities provide many physiological functions to their hosts, especially in herbivorous animals. We still lack an understanding of how these microbial communities are structured across hosts in nature, especially within a given host species. Studies on laboratory mice have demonstrated that host genetics can influence microbial community structure, but that diet can overwhelm these genetic effects. We aimed to test these ideas in a natural system, the American pika (Ochotona princeps). First, pikas are high-elevation specialists with significant population structure across various mountain ranges in the USA, allowing us to investigate whether similarities in microbial communities match host genetic differences. Additionally, pikas are herbivorous, with some populations exhibiting remarkable dietary plasticity and consuming high levels of moss, which is exceptionally high in fibre and low in protein. This allows us to investigate adaptations to an herbivorous diet, as well as to the especially challenging diet of moss. Here, we inventoried the microbial communities of pika caecal pellets from various populations using 16S rRNA sequencing to investigate structuring of microbial communities across various populations with different natural diets. Microbial communities varied significantly across populations, and differences in microbial community structure were congruent with genetic differences in host population structure, a pattern known as "phylosymbiosis." Several microbial members (Ruminococcus, Prevotella, Oxalobacter and Coprococcus) were detected across all samples, and thus likely represent a "core microbiome." These genera are known to perform a number of services for herbivorous hosts such as fibre fermentation and the degradation of plant defensive compounds, and thus are likely important for herbivory in pikas. Moreover, pikas that feed on moss harboured microbial communities highly enriched in Melainabacteria. This uncultivable candidate phylum has been proposed to ferment fibre for herbivores, and thus may contribute to the ability of some pika populations to consume high amounts of moss. These findings demonstrate that both host genetics and diet can influence the microbial communities of the American pika. These animals may be novel sources of fibre-degrading microbes. Last, we discuss the implications of population-specific microbial communities for conservation efforts in this species.
肠道微生物群落为其宿主提供许多生理功能,尤其是在草食性动物中。我们仍然缺乏对这些微生物群落如何在自然界中跨宿主构建的理解,特别是在特定宿主物种内。对实验室小鼠的研究表明,宿主遗传可以影响微生物群落结构,但饮食可以压倒这些遗传影响。我们旨在在自然系统中测试这些想法,即美洲旱獭(Ochotona princeps)。首先,旱獭是高海拔的专家,在美国的各个山脉中存在着显著的种群结构,这使我们能够研究微生物群落的相似性是否与宿主遗传差异相匹配。此外,旱獭是草食性动物,有些种群具有显著的饮食可塑性,并且会食用高水平的苔藓,而苔藓的纤维含量特别高,蛋白质含量特别低。这使我们能够研究对草食性饮食的适应,以及对特别具有挑战性的苔藓饮食的适应。在这里,我们使用 16S rRNA 测序对来自不同种群的旱獭盲肠粪球的微生物群落进行了编目,以调查具有不同天然饮食的不同种群的微生物群落结构。微生物群落在种群之间差异显著,微生物群落结构的差异与宿主种群结构的遗传差异一致,这种模式被称为“共生进化”。在所有样本中都检测到了几个微生物成员(Ruminococcus、Prevotella、Oxalobacter 和 Coprococcus),因此它们可能代表一个“核心微生物组”。这些属已知为草食性宿主提供许多服务,例如纤维发酵和植物防御化合物的降解,因此它们可能对旱獭的草食性很重要。此外,以苔藓为食的旱獭体内的微生物群落高度富含 Melainabacteria。这种未培养的候选门被认为可以为草食动物发酵纤维,因此可能有助于一些旱獭种群消耗大量苔藓的能力。这些发现表明,宿主遗传和饮食都可以影响美洲旱獭的微生物群落。这些动物可能是纤维降解微生物的新来源。最后,我们讨论了种群特异性微生物群落对该物种保护工作的影响。