Associations Between Gut Microbiota Diversity and a Host Fitness Proxy in a Naturalistic Experiment Using Threespine Stickleback Fish

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Andreas Härer, Ken A. Thompson, Dolph Schluter, Diana J. Rennison
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引用次数: 0

Abstract

The vertebrate gut microbiota is a critical determinant of organismal function, yet whether and how gut microbial communities affect host fitness under natural conditions remains largely unclear. We characterised associations between a fitness proxy—individual growth rate—and bacterial gut microbiota diversity and composition in threespine stickleback fish introduced to large semi-natural ponds. We detected a 63% higher richness of bacterial taxa (α-diversity) in the guts of high-fitness fish compared to low-fitness fish, which might be driven by stronger bacterial dispersal among high-fitness fish according to the fit of a neutral community model. Further, microbial communities of high-fitness fish were more similar to one another (i.e., exhibited lower β-diversity) than those of low-fitness fish. The lower β-diversity found to be associated with higher host fitness is consistent with the Anna Karenina principle—that there are fewer ways to have a functional microbiota than a dysfunctional microbiota. Our study links differences in α- and β-diversity to a fitness-related trait in a vertebrate species reared under naturalistic conditions and our findings provide a basis for functional tests of the fitness consequences of host-microbiota interactions.

Abstract Image

利用三刺棒背鱼进行的自然实验中肠道微生物群多样性与宿主体质替代物之间的关系
脊椎动物肠道微生物群是决定生物体功能的关键因素,但在自然条件下,肠道微生物群落是否以及如何影响宿主的体能,目前仍不清楚。我们研究了被引入大型半自然池塘的三刺鱼的个体生长率与细菌肠道微生物群多样性和组成之间的关系。与低适生性鱼类相比,我们发现高适生性鱼类肠道中细菌类群的丰富度(α-多样性)高出63%,根据中性群落模型的拟合,这可能是由于高适生性鱼类之间的细菌扩散能力更强。此外,高体能鱼类的微生物群落比低体能鱼类的微生物群落更相似(即表现出较低的β-多样性)。发现较低的β-多样性与较高的宿主适合度相关,这与安娜-卡列尼娜原则是一致的,即拥有一个功能性微生物群的方法比拥有一个功能失调的微生物群的方法要少。我们的研究将在自然条件下饲养的脊椎动物物种的 α 和 β 多样性差异与适应性相关特征联系起来,我们的发现为宿主-微生物群相互作用的适应性后果的功能测试提供了基础。
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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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