SubCom analysis: dissecting microbial community functions into taxon-specific contributions and interaction contexts.

IF 14.9 1区 生物学 Q1 MICROBIOLOGY
Hidehiro Ishizawa, Miku Kito, Sunao Noguchi, Kodai Kimura, Masahiro Takeo
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引用次数: 0

Abstract

Background: Microbial communities play fundamental roles in industrial processes and ecosystem stability. However, understanding how individual members and their interactions give rise to community-level function remains challenging because such functions emerge from complex interactions among diverse members.

Results: In this study, we developed SubCom analysis, a subcommunity-based experimental-computational workflow for inferring candidate taxon-specific contributions and interaction contexts underlying microbial community function. Using an aniline-degrading microbial community, we generated paired composition-function data from 558 randomly assembled, low-complexity subcommunities constructed using a dilution-and-dispense strategy. We then trained decision-tree-based models to predict community function from composition, achieving high predictive performance (r = 0.77-0.89). Interpretation of the learned decision rules identified taxa with consistent functional association: specific Pseudomonas and Acinetobacter taxa were associated with increased community-level aniline utilization, whereas an Achromobacter taxon exhibited a negative association despite its presumed role in downstream metabolism. The models further suggested potential functional interactions, including attenuation of the positive contributions of Pseudomonas and Acinetobacter in the presence of a Corynebacterium taxon, highlighting functional relationships that are not readily inferred from genome-based approaches alone. An augmentation assay using representative isolates supported the predicted direction of several effects and enabled targeted improvement of community function.

Conclusions: These results demonstrate the potential of SubCom analysis as a practical framework for inferring taxon-specific contributions and interaction contexts in complex, nonsynthetic microbial communities. Video Abstract.

SubCom分析:将微生物群落功能分解为分类群特定贡献和相互作用背景。
背景:微生物群落在工业过程和生态系统稳定中起着重要作用。然而,理解个体成员及其相互作用如何产生社区级功能仍然具有挑战性,因为这些功能来自不同成员之间复杂的相互作用。结果:在这项研究中,我们开发了SubCom分析,这是一种基于亚社区的实验计算工作流,用于推断候选分类群特异性贡献和微生物群落功能背后的相互作用背景。利用苯胺降解微生物群落,我们使用稀释-分配策略从558个随机组装的低复杂性亚群落中生成配对的组成函数数据。然后,我们训练基于决策树的模型来预测群落组成的功能,获得了很高的预测性能(r = 0.77-0.89)。通过对所学决策规则的解释,确定了具有一致功能关联的分类群:特定的假单胞菌和不动杆菌分类群与群落水平苯胺利用率增加相关,而无色杆菌分类群表现出负相关,尽管其被认为在下游代谢中起作用。这些模型进一步表明了潜在的功能相互作用,包括在棒状杆菌分类群存在时假单胞菌和不动杆菌的积极贡献的减弱,突出了仅通过基于基因组的方法不易推断出的功能关系。使用代表性分离株进行的扩增试验支持了几种效应的预测方向,并能够有针对性地改善群落功能。结论:这些结果显示了SubCom分析作为推断复杂的非合成微生物群落中分类群特异性贡献和相互作用背景的实用框架的潜力。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
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.
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