Jake Williams, Nathalie Pettorelli, Aaron C. Hartmann, Robert A. Quinn, Laetitia Plaisance, Michael O’Mahoney, Chris P. Meyer, Katharina E. Fabricius, Nancy Knowlton, Emma Ransome
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引用次数: 0
Abstract
Microbes play vital roles across coral reefs both in the environment and inside and upon macrobes (holobionts), where they support critical functions such as nutrition and immune system modulation. These roles highlight the potential ecosystem-level importance of microbes, yet most knowledge of microbial functions on reefs is derived from a small set of holobionts such as corals and sponges. Declining seawater pH — an important global coral reef stressor — can cause ecosystem-level change on coral reefs, providing an opportunity to study the role of microbes at this scale. We use an in situ experimental approach to test the hypothesis that under such ocean acidification (OA), known shifts among macrobe trophic and functional groups may drive a general ecosystem-level response extending across macrobes and microbes, leading to reduced distinctness between the benthic holobiont community microbiome and the environmental microbiome. We test this hypothesis using genetic and chemical data from benthic coral reef community holobionts sampled across a pH gradient from CO2 seeps in Papua New Guinea. We find support for our hypothesis; under OA, the microbiome and metabolome of the benthic holobiont community become less compositionally distinct from the sediment microbiome and metabolome, suggesting that benthic macrobe communities are colonised by environmental microbes to a higher degree under OA conditions. We also find a simplification and homogenisation of the benthic photosynthetic community, and an increased abundance of fleshy macroalgae, consistent with previously observed reef microbialisation. We demonstrate a novel structural shift in coral reefs involving macrobes and microbes: that the microbiome of the benthic holobiont community becomes less distinct from the sediment microbiome under OA. Our findings suggest that microbialisation and the disruption of macrobe trophic networks are interwoven general responses to environmental stress, pointing towards a universal, undesirable, and measurable form of ecosystem changed.
微生物在整个珊瑚礁的环境、大型生物(整体生物)内部和其上都发挥着至关重要的作用,支持着营养和免疫系统调节等关键功能。这些作用凸显了微生物在生态系统层面的潜在重要性,然而有关珊瑚礁上微生物功能的大部分知识都来自珊瑚和海绵等一小部分整体生物。海水 pH 值的下降是全球珊瑚礁面临的一个重要压力,它能引起珊瑚礁生态系统层面的变化,从而为研究微生物在这一尺度上的作用提供了机会。我们采用原位实验的方法来验证这样一个假设:在这种海洋酸化(OA)的情况下,已知的大型生物营养群和功能群之间的变化可能会驱动一种扩展到大型生物和微生物的总体生态系统级响应,从而导致底栖整体生物群落微生物组和环境微生物组之间的差异减小。我们利用从巴布亚新几内亚二氧化碳渗流的 pH 值梯度上采样的底栖珊瑚礁群落全生物体的遗传和化学数据来验证这一假设。我们发现我们的假设得到了支持;在 OA 条件下,底栖整体生物群落的微生物组和代谢组与沉积物微生物组和代谢组的组成差异越来越小,这表明在 OA 条件下,底栖大型生物群落被环境微生物定殖的程度更高。我们还发现底栖光合群落的简化和同质化,以及肉质大型藻类数量的增加,这与之前观察到的珊瑚礁微生物化是一致的。我们证明了珊瑚礁中涉及大型生物和微生物的一种新的结构转变:在 OA 条件下,底栖整体生物群落的微生物组与沉积物微生物组的区别越来越小。我们的研究结果表明,微生物化和大型生物营养网络的破坏是相互交织的对环境压力的一般反应,指向一种普遍的、不可取的和可测量的生态系统变化形式。
期刊介绍:
Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.