Interplay between antipredator behavior, parasitism, and gut microbiome in wild stickleback populations.

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Javier Edo Varg, Jaelle C Brealey, David Benhaïm, Rafael Losada-Germain, Janette W Boughman
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Abstract

The impact of microbial composition on stress-related behavior in aquatic organisms is poorly understood. This study explored the link between antipredator behavior, parasitism, and the gut microbiome in wild stickleback from two lakes: clear, spring-fed Galtaból and turbid, glacial-fed Þristikla. Behavioral analysis revealed differences between populations, with each exhibiting unique baseline behaviors. Microbiome analysis showed that a small proportion of its variation was explained by population, likely reflecting differences in lake environments. Only the marine genus Pseudoalteromonas abundance differed between populations. Our findings suggest that behavior and microbiome correlations may primarily reflect environmental adaptations and parasite status rather than direct gut-brain interactions. However, some tentative evidence suggests a potential innate connection between some antipredator behavior and microbiome composition. The study highlights the complexity of the gut-brain axis in wild populations and suggests future research directions, including experimental manipulations to uncover causal relationships between microbiome composition and behavior.

野生棘鱼种群抗捕食行为、寄生和肠道微生物群之间的相互作用。
微生物组成对水生生物应激相关行为的影响尚不清楚。这项研究探索了来自两个湖泊的野生刺鱼的反捕食行为、寄生和肠道微生物群之间的联系:清澈的、泉水喂养的Galtaból和浑浊的、冰川喂养的Þristikla。行为分析揭示了种群之间的差异,每个种群都表现出独特的基线行为。微生物组分析表明,它的一小部分变化可以用种群来解释,这可能反映了湖泊环境的差异。在不同种群间,只有海洋假互交单胞菌属的丰度存在差异。我们的研究结果表明,行为和微生物组的相关性可能主要反映了环境适应和寄生虫状态,而不是直接的肠-脑相互作用。然而,一些初步证据表明,一些反捕食者行为与微生物组组成之间存在潜在的先天联系。该研究强调了野生种群肠脑轴的复杂性,并提出了未来的研究方向,包括通过实验操作来揭示微生物组组成和行为之间的因果关系。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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