与浮游植物相关的微生物组内的生物多样性调节宿主生理、宿主群落生态和营养循环。

IF 5.2 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-02-18 Epub Date: 2025-01-28 DOI:10.1128/msystems.01462-24
Jonathan R Dickey, Nikki M Mercer, Mirte C M Kuijpers, Ruben Props, Sara L Jackrel
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引用次数: 0

摘要

包括原核生物在内的整个生命之树的生物多样性正在下降。随着人们越来越认识到宿主相关微生物是真核宿主生理、行为和生态的潜在调节因子,了解宿主微生物组多样性下降对宿主适应性、生态学和生态系统功能的影响是很重要的。我们使用浮游植物及其相关的环境微生物组作为模型系统来测试微生物组多样性下降的独立和相互作用效应,这些影响通常是由人类活动引起的温度升高和营养物质可用性的改变。我们发现低微生物组多样性对宿主生理、浮游植物群落动态和养分循环的影响。微生物组多样性降低导致宿主细胞应激加剧,如δ13C和δ15N升高所示。微生物组多样性也显著影响宿主细胞形态指标,可能是这种对细胞应激的影响的结果。低微生物群落多样性对寄主群落生态的影响包括浮游植物群落多样性和生物量的升高。这些宿主相关微生物的多样性还对生态系统养分循环具有级联影响,其中微生物组多样性降低导致环境中总溶解N和P的耗竭。由微生物组多样性引起的这些影响的程度在营养枯竭的环境和高温下最大。我们的研究结果强调了宿主相关微生物多样性从宿主细胞生理到生态系统营养循环的广泛影响。在经历由人为活动引起的多重压力源的生态系统中,微生物组多样性下降的这些已证实的影响可能会被放大。重要性:随着越来越多的证据表明宿主相关微生物组在调节真核宿主的生理、适应性和生态方面发挥关键作用,人类活动正在导致生物多样性的下降,包括微生物世界。在这里,我们使用一个多因素操纵实验来测试宿主微生物组多样性下降的影响,无论是单独的还是与新兴的全球变化的影响相结合,包括气候变暖和营养物质生物利用度的变化,这些变化正在对宿主生物造成越来越多的非生物压力。利用携带外部微生物组的单细胞真核浮游植物作为模型系统,我们证明了宿主相关微生物组的多样性影响多层生物组织,包括宿主生理学、宿主种群和群落生态学以及生态系统营养循环。值得注意的是,这些微生物组多样性驱动的效应在非生物应激环境中被放大,这表明微生物组多样性的重要性可能在人类世期间随着时间的推移而增加。
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Biodiversity within phytoplankton-associated microbiomes regulates host physiology, host community ecology, and nutrient cycling.

Biological diversity is declining across the tree of life, including among prokaryotes. With the increasing awareness of host-associated microbes as potential regulators of eukaryotic host physiology, behavior, and ecology, it is important to understand the implications of declining diversity within host microbiomes on host fitness, ecology, and ecosystem function. We used phytoplankton and their associated environmental microbiomes as model systems to test the independent and interactive effects of declining microbiome diversity with and without other stressors often caused by human activity-elevated temperature and altered nutrient availability. We found effects of low microbiome diversity on host physiology, phytoplankton community dynamics, and nutrient cycling. Low microbiome diversity caused greater host cellular stress, as indicated by elevated δ13C and δ15N. Microbiome diversity also significantly affected host cell morphological metrics, likely as a consequence of this effect on cell stress. Despite causing greater host cellular stress, the effects of low microbiome diversity on host community ecology included elevated phytoplankton community diversity and biomass. The diversity of these host-associated microbes also had cascading implications on ecosystem nutrient cycling, where lower microbiome diversity caused a depletion of total dissolved N and P in the environment. The magnitude of these effects, caused by microbiome diversity, was greatest among nutrient-depleted environments and at elevated temperatures. Our results emphasize the widespread implications of declining host-associated microbial diversity from host cellular physiology to ecosystem nutrient cycling. These demonstrated effects of declining microbiome diversity are likely to be amplified in ecosystems experiencing multiple stressors caused by anthropogenic activities.

Importance: As evidence is emerging of the key roles that host-associated microbiomes often play in regulating the physiology, fitness, and ecology of their eukaryotic hosts, human activities are causing declines in biological diversity, including within the microbial world. Here, we use a multifactorial manipulative experiment to test the effects of declining diversity within host microbiomes both alone and in tandem with the effects of emerging global changes, including climate warming and shifts in nutrient bioavailability, which are inflicting increasing abiotic stress on host organisms. Using single-celled eukaryotic phytoplankton that harbor an external microbiome as a model system, we demonstrate that diversity within host-associated microbiomes impacts multiple tiers of biological organization, including host physiology, the host population and community ecology, and ecosystem nutrient cycling. Notably, these microbiome diversity-driven effects became magnified in abiotically stressful environments, suggesting that the importance of microbiome diversity may have increased over time during the Anthropocene.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
期刊最新文献
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