野生北方哺乳动物的种群动态和微生物组:雪鞋兔周期和饮食、季节和捕食风险的影响。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mason R. Stothart, Sophia Lavergne, Laura McCaw, Hardeep Singh, Wilfred de Vega, Katherine Amato, Jocelyn Poissant, Rudy Boonstra
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引用次数: 0

摘要

北美北方森林是一个巨大的生态系统,其主要食草动物是雪靴兔(Lepus americanus)。野兔在饮食、天气、食物供应和捕食风险方面都面临着相当极端的环境。肠道微生物群被认为可以促进动物对环境变化的适应性反应,但对体内平衡的严重环境挑战也会破坏宿主-微生物群的关系。为了更好地理解肠道微生物组对动物适应的贡献,我们研究了野生野兔在两种极端环境变化下的粪便细菌微生物组,这两种极端环境变化是它们自然史中不可或缺的:(1)夏季和冬季之间的季节性转变,以及(2)以食物资源可用性和捕食压力的变化为特征的~10年“盛衰”种群周期的变化。与夏季相比,冬季野兔的细菌丰富度较低,20个科(包括草藻科和Christensenellaceae)的细菌数量减少,但Ruminococcaceae(含有植物纤维降解细菌的科)和其他9个细菌群的细菌数量增加。在种群周期的不同阶段也出现了明显的细菌微生物组差异。与种群周期的上升和下降阶段相比,高峰时期细菌微生物组丰富度较低,组成差异明显。宿主生理和饮食质量(粪便纤维含量)的直接测量最有力地支持食物资源可用性是细菌群落基于阶段差异的机制,但粪便纤维含量不能完全解释细菌微生物组在不同阶段的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Population Dynamics and the Microbiome in a Wild Boreal Mammal: The Snowshoe Hare Cycle and Impacts of Diet, Season and Predation Risk

Population Dynamics and the Microbiome in a Wild Boreal Mammal: The Snowshoe Hare Cycle and Impacts of Diet, Season and Predation Risk

The North American boreal forest is a massive ecosystem, and its keystone herbivore is the snowshoe hare (Lepus americanus). Hares are exposed to considerable environmental extremes in diet and weather, food availability, and predation risk. Gut microbiomes have been suggested to facilitate adaptive animal responses to environmental change, but severe environmental challenges to homeostasis can also disrupt host-microbiome relationships. To better understand gut microbiome contributions to animal acclimation, we studied the faecal bacterial microbiome of wild hares across two types of extreme environmental change that are integral to their natural history: (1) seasonal transitions between summer and winter, and (2) changes over the ~10 year ‘boom-bust’ population cycles that are characterised by shifting food resource availability and predation pressure. When compared to summer, hares in winter had lower bacterial richness and were depleted in 20 families (including Oxalobacteraceae and Christensenellaceae) but enriched for Ruminococcaceae (a family which contains plant fibre degrading bacteria) alongside nine other bacterial groups. Marked bacterial microbiome differences also occurred across phases of the population cycle. Bacterial microbiomes were lower in richness and compositionally distinct in the peak compared to the increase or decline phases of the population cycle. Direct measures of host physiology and diet quality (faecal fibre contents) most strongly supported food resource availability as a mechanism underlying phase-based differences in bacterial communities, but faecal fibre contents could not fully account for bacterial microbiome variation across phases.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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