{"title":"Learning the mechanism of collective microbial function via random community-media pairing.","authors":"Luoqi Wang, Seppe Kuehn, Mikhail Tikhonov","doi":"10.1088/1478-3975/aeb3c4","DOIUrl":null,"url":null,"abstract":"<p><p>In microbial systems, many biochemical functions arise from pathways encoded and executed at the community level. The collective nature of these functions complicates bottom-up efforts to determine each species' contribution. Previous work has shown that regression over randomly sampled datasets of collective functions succeeds at predicting those functions. Building on this top-down idea, this paper asks whether regression can also reveal mechanistic insight into a cross-feeding relationship. For this, we propose extending the random sampling method to vary the growth environment, cultivating each community in the spent medium of another randomly constructed community. Using a model-based analysis, we illustrate that the mechanistic roles of species are structurally non-identifiable under the standard random sampling protocol, but become identifiable after the proposed modification, such that even a simple LASSO regression can recover them. More generally, our work suggests that the utility of machine-learning-based approaches can be greatly enhanced by a synergistic experimental design.</p>","PeriodicalId":20207,"journal":{"name":"Physical biology","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2026-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1088/1478-3975/aeb3c4","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
In microbial systems, many biochemical functions arise from pathways encoded and executed at the community level. The collective nature of these functions complicates bottom-up efforts to determine each species' contribution. Previous work has shown that regression over randomly sampled datasets of collective functions succeeds at predicting those functions. Building on this top-down idea, this paper asks whether regression can also reveal mechanistic insight into a cross-feeding relationship. For this, we propose extending the random sampling method to vary the growth environment, cultivating each community in the spent medium of another randomly constructed community. Using a model-based analysis, we illustrate that the mechanistic roles of species are structurally non-identifiable under the standard random sampling protocol, but become identifiable after the proposed modification, such that even a simple LASSO regression can recover them. More generally, our work suggests that the utility of machine-learning-based approaches can be greatly enhanced by a synergistic experimental design.
期刊介绍:
Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity.
Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as:
molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions
subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure
intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division
systems biology, e.g. signaling, gene regulation and metabolic networks
cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms
cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis
cell-cell interactions, cell aggregates, organoids, tissues and organs
developmental dynamics, including pattern formation and morphogenesis
physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation
neuronal systems, including information processing by networks, memory and learning
population dynamics, ecology, and evolution
collective action and emergence of collective phenomena.