Dynamic linear models guide design and analysis of microbiota studies within artificial human guts

Justin D. Silverman, Heather K. Durand, Rachael J. Bloom, Sayan Mukherjee, Lawrence A. David

Research output: Contribution to journalArticlepeer-review

51 Scopus citations

Abstract

Background: Artificial gut models provide unique opportunities to study human-associated microbiota. Outstanding questions for these models' fundamental biology include the timescales on which microbiota vary and the factors that drive such change. Answering these questions though requires overcoming analytical obstacles like estimating the effects of technical variation on observed microbiota dynamics, as well as the lack of appropriate benchmark datasets. Results: To address these obstacles, we created a modeling framework based on multinomial logistic-normal dynamic linear models (MALLARDs) and performed dense longitudinal sampling of four replicate artificial human guts over the course of 1 month. The resulting analyses revealed how the ratio of biological variation to technical variation from sample processing depends on sampling frequency. In particular, we find that at hourly sampling frequencies, 76% of observed variation could be ascribed to technical sources, which could also skew the observed covariation between taxa. We also found that the artificial guts demonstrated replicable trajectories even after a recovery from a transient feed disruption. Additionally, we observed irregular sub-daily oscillatory dynamics associated with the bacterial family Enterobacteriaceae within all four replicate vessels. Conclusions: Our analyses suggest that, beyond variation due to sequence counting, technical variation from sample processing can obscure temporal variation from biological sources in artificial gut studies. Our analyses also supported hypotheses that human gut microbiota fluctuates on sub-daily timescales in the absence of a host and that microbiota can follow replicable trajectories in the presence of environmental driving forces. Finally, multiple aspects of our approach are generalizable and could ultimately be used to facilitate the design and analysis of longitudinal microbiota studies in vivo.

Original languageEnglish
Article number202
JournalMicrobiome
Volume6
Issue number1
DOIs
StatePublished - 12 Nov 2018
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2018 The Author(s).

Funding

JDS and LAD acknowledge support from the Duke University Medical Scientist Training Program (GM007171), the Global Probiotics Council, a Searle Scholars Award, the Hartwell Foundation, an Alfred P. Sloan Research Fellowship, the Translational Research Institute through Cooperative Agreement NNX16AO69A, the Damon Runyon Cancer Research Foundation, the Hartwell Foundation, and NIH 1R01DK116187-01. SM would like to acknowledge the support of grants NSF IIS-1546331, NSF DMS-1418261, NSF IIS-1320357, NSF DMS-1045153, and NSF DMS1613261. We thank Rachel Silverman, Alex D. Washburne, Lionel Watkins, Firas Midani, Max Villa, Zachary Holmes, Brianna Petrone, B. Jesse Shapiro, Jonathan Friedman, and Susan Holmes for their manuscript comments and insights. This work used a high-performance computing facility partially supported by grant 2016-IDG-1013 (“HARDAC+: Reproducible HPC for Next-generation Genomics”) from the North Carolina Biotechnology Center.

FundersFunder number
Global Probiotics Council
National Science FoundationIIS-1546331, DMS-1418261, DMS-1045153, DMS1613261, IIS-1320357
National Institutes of Health
National Institute of Diabetes and Digestive and Kidney DiseasesR01DK116187
Alfred P. Sloan Foundation
Damon Runyon Cancer Research Foundation
North Carolina Biotechnology Center
Duke UniversityGM007171
Hartwell Foundation
Translational Research Institute, University of Arkansas for Medical SciencesNNX16AO69A

    Keywords

    • Artificial gut
    • Bayesian statistics
    • Bioreactor
    • Compositional data
    • Metagenomics
    • Microbiome
    • Time series analysis

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