多组学分析揭示了金属相互作用中Botryllus schlosseri微生物衍生代谢产物的重要作用。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-15 DOI:10.1128/msystems.00793-25
Dulce G Guillén Matus, Caroline M Donaghy, Nidhi Vijayan, Zachary T Lane, Matthew Howell, George G Glavin, Alfredo M Angeles-Boza, Spencer V Nyholm, Marcy J Balunas
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引用次数: 0

摘要

海洋微生物群落控制着海洋中的许多生物和化学过程,包括元素循环、生态系统健康和疾病。海洋生物被微生物包围,细菌共生体、真核宿主及其病原体或猎物之间发生复杂的分子相互作用。海洋中的微量金属可能对海洋生物有益,也可能有害,这取决于它们的浓度和生物利用度。已知多种海洋被囊动物在其地幔中生物积累微量金属,研究表明被囊动物微生物群在这一过程中起着重要作用。作为一种海洋群居被囊动物,猪囊藻已成为细胞和发育研究的模式生物,但其生态相互作用仍未得到很好的了解。采用综合多学科方法,我们建立了一个全面的基线,并探索了schlosseb微生物组,代谢组和金属组成员之间的相关性,以阐明微量金属在宿主-微生物-病原体相互作用中的生态效应。我们发现金属(包括锰、镍、铈、锌和钴)与各种代谢物和细菌分类群之间存在显著相关性。这些发现有助于深入了解schlosseri与微生物及其环境的生物和化学相互作用,有助于弥合宿主-微生物组-环境相互作用的知识空白,并为微量金属在这些生物系统中的生态效应的进一步研究奠定基础。鉴于海洋无脊椎动物及其微生物群落在海洋生态系统中的重要性,我们试图描述海洋殖民地被囊动物Botryllus schlosseri(一种用于细胞和发育研究的模式生物)大部分未知的微生物关联、金属封存和代谢物产生。利用综合多学科方法,我们确定了金属、代谢物和细菌分类群之间的显著相关性。与海水相比,schlos螺旋体组织中金属含量高,微生物组β多样性与海水差异显著。我们还引入了泛代谢组的概念,根据复杂样品中代谢物的存在与否对其进行分类,并在核心代谢组和灵活代谢组中发现了微生物代谢物。这些发现有助于深入了解schlosseri与微生物及其环境的生物和化学相互作用,弥补了宿主-微生物组-环境相互作用的知识空白,并为微量金属在这些生物系统中的生态效应的进一步研究奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-omics analysis reveals important role for microbial-derived metabolites from Botryllus schlosseri in metal interactions.

Marine microbial communities govern many of the biological and chemical processes in the ocean, including element cycles, ecosystem health, and disease. Marine organisms are surrounded by microbes, with complex molecular interactions occurring between bacterial symbionts, eukaryotic hosts, and their pathogens or prey. Trace metals in the ocean can be either beneficial or detrimental to marine life depending on their concentrations and bioavailability. Multiple marine tunicate species are known to bioaccumulate trace metals in their mantel, and research suggests that tunicate microbiota plays an important role in this process. Botryllus schlosseri, a marine colonial tunicate, has become a model organism for cellular and developmental studies, yet its ecological interactions are still not well understood. Using an integrated multidisciplinary approach, we established a comprehensive baseline and explored correlations between members of the B. schlosseri microbiome, metabolome, and metallome to elucidate the ecological effects of trace metals in host-microbe-pathogen interactions. We identified significant correlations between metals, including manganese, nickel, cerium, zinc, and cobalt, with various metabolites and bacterial taxa. These findings offer insights into B. schlosseri's biological and chemical interactions with microorganisms and their environment, contributing to bridging the knowledge gap of host-microbiome-environment interactions and establishing a foundation for continuing research on the ecological effects of trace metals in these biological systems.IMPORTANCEGiven the importance of marine invertebrates and their microbial communities in marine ecosystems, we sought to characterize the largely unknown microbial associates, metal sequestration, and metabolite production of the marine colonial tunicate, Botryllus schlosseri, a model organism for cellular and developmental studies. Using an integrated multidisciplinary approach, we identified significant correlations between metals, metabolites, and bacterial taxa. B. schlosseri tissue was highly enriched in metals compared to seawater, and B. schlosseri microbiome beta-diversity was significantly different from seawater. We also introduced the concept of the pan-metabolome to classify metabolites based on their presence or absence across complex samples and found microbial metabolites in both the core and flexible metabolome. These findings offer insights into B. schlosseri's biological and chemical interactions with microorganisms and their environment, bridging the knowledge gap of host-microbiome-environment interactions and establishing a foundation for continuing research on the ecological effects of trace metals in these biological systems.

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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.
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