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      Defining and Evaluating Microbial Contributions to Metabolite Variation in Microbiome-Metabolome Association Studies

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          Abstract

          Identifying the key microbial taxa responsible for metabolic differences between microbiomes is an important step toward understanding and manipulating microbiome metabolism. To achieve this goal, researchers commonly conduct microbiome-metabolome association studies, comprehensively measuring both the composition of species and the concentration of metabolites across a set of microbial community samples and then testing for correlations between microbes and metabolites. Here, we evaluated the utility of this general approach by first developing a rigorous mathematical definition of the contribution of each microbial taxon to metabolite variation and then examining these contributions in simulated data sets of microbial community metabolism. We found that standard correlation-based analysis of our simulated microbiome-metabolome data sets can identify true contributions with very low predictive value and that its performance depends strongly on specific properties of both metabolites and microbes, as well as on those of the surrounding environment. Combined, our findings can guide future interpretation and validation of microbiome-metabolome studies.

          ABSTRACT

          Correlation-based analysis of paired microbiome-metabolome data sets is becoming a widespread research approach, aiming to comprehensively identify microbial drivers of metabolic variation. To date, however, the limitations of this approach and other microbiome-metabolome analysis methods have not been comprehensively evaluated. To address this challenge, we have introduced a mathematical framework to quantify the contribution of each taxon to metabolite variation based on uptake and secretion fluxes. We additionally used a multispecies metabolic model to simulate simplified gut communities, generating idealized microbiome-metabolome data sets. We then compared observed taxon-metabolite correlations in these data sets to calculated ground truth taxonomic contribution values. We found that in simulations of both a representative simple 10-species community and complex human gut microbiota, correlation-based analysis poorly identified key contributors, with an extremely low predictive value despite the idealized setting. We further demonstrate that the predictive value of correlation analysis is strongly influenced by both metabolite and taxon properties, as well as by exogenous environmental variation. We finally discuss the practical implications of our findings for interpreting microbiome-metabolome studies.

          IMPORTANCE Identifying the key microbial taxa responsible for metabolic differences between microbiomes is an important step toward understanding and manipulating microbiome metabolism. To achieve this goal, researchers commonly conduct microbiome-metabolome association studies, comprehensively measuring both the composition of species and the concentration of metabolites across a set of microbial community samples and then testing for correlations between microbes and metabolites. Here, we evaluated the utility of this general approach by first developing a rigorous mathematical definition of the contribution of each microbial taxon to metabolite variation and then examining these contributions in simulated data sets of microbial community metabolism. We found that standard correlation-based analysis of our simulated microbiome-metabolome data sets can identify true contributions with very low predictive value and that its performance depends strongly on specific properties of both metabolites and microbes, as well as on those of the surrounding environment. Combined, our findings can guide future interpretation and validation of microbiome-metabolome studies.

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          The Community Climate System Model Version 3 (CCSM3)

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            Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox v2.0.

            Over the past decade, a growing community of researchers has emerged around the use of constraint-based reconstruction and analysis (COBRA) methods to simulate, analyze and predict a variety of metabolic phenotypes using genome-scale models. The COBRA Toolbox, a MATLAB package for implementing COBRA methods, was presented earlier. Here we present a substantial update of this in silico toolbox. Version 2.0 of the COBRA Toolbox expands the scope of computations by including in silico analysis methods developed since its original release. New functions include (i) network gap filling, (ii) (13)C analysis, (iii) metabolic engineering, (iv) omics-guided analysis and (v) visualization. As with the first version, the COBRA Toolbox reads and writes systems biology markup language-formatted models. In version 2.0, we improved performance, usability and the level of documentation. A suite of test scripts can now be used to learn the core functionality of the toolbox and validate results. This toolbox lowers the barrier of entry to use powerful COBRA methods.
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              Generation of genome-scale metabolic reconstructions for 773 members of the human gut microbiota

              A large set of microbial metabolic models (AGORA) could be applied to better understand the functions of the human gut microbiome.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mSystems
                mSystems
                msys
                msys
                mSystems
                mSystems
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2379-5077
                Nov-Dec 2019
                17 December 2019
                : 4
                : 6
                : e00579-19
                Affiliations
                [a ]Department of Genome Sciences, University of Washington, Seattle, Washington, USA
                [b ]Department of Computer Science and Engineering, University of Washington, Seattle, Washington, USA
                [c ]Blavatnik School of Computer Science, Tel Aviv University, Tel Aviv, Israel
                [d ]Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
                [e ]Santa Fe Institute, Santa Fe, New Mexico, USA
                Mayo Clinic
                Author notes
                Address correspondence to Elhanan Borenstein, elbo@ 123456uw.edu .
                [*]

                Present address: Cecilia Noecker, Department of Microbiology and Immunology, University of California San Francisco, San Francisco, California, USA; Hsuan-Chao Chiu, MediaTek Inc., Hsinchu City, Taiwan.

                Citation Noecker C, Chiu H-C, McNally CP, Borenstein E. 2019. Defining and evaluating microbial contributions to metabolite variation in microbiome-metabolome association studies. mSystems 4:e00579-19. https://doi.org/10.1128/mSystems.00579-19.

                Author information
                https://orcid.org/0000-0003-1417-2383
                Article
                mSystems00579-19
                10.1128/mSystems.00579-19
                6918031
                31848305
                aae4be60-5ae5-4cbc-8909-85e482c1e2e5
                Copyright © 2019 Noecker et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 8 September 2019
                : 20 November 2019
                Page count
                supplementary-material: 10, Figures: 7, Tables: 0, Equations: 20, References: 94, Pages: 28, Words: 20732
                Funding
                Funded by: NIH;
                Award ID: New Innovator Award DP2 AT007802-01
                Award ID: 1R01GM124312-01
                Award Recipient :
                Funded by: National Science Foundation (NSF), https://doi.org/10.13039/100000001;
                Award ID: IGERT DGE-1258485
                Award Recipient :
                Funded by: HHS | NIH | National Human Genome Research Institute (NHGRI), https://doi.org/10.13039/100000051;
                Award ID: T32 HG000035
                Award Recipient :
                Categories
                Research Article
                Novel Systems Biology Techniques
                Custom metadata
                November/December 2019

                correlation,evaluation,metabolic modeling,metabolomics,microbiome

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