Development of Inflammatory Bowel Disease Is Linked to a Longitudinal Restructuring of the Gut Metagenome in Mice

Author:

Sharpton Thomas12,Lyalina Svetlana3,Luong Julie3,Pham Joey3,Deal Emily M.3,Armour Courtney1,Gaulke Christopher1,Sanjabi Shomyseh34,Pollard Katherine S.35

Affiliation:

1. Department of Microbiology, Oregon State University, Corvallis, Oregon

2. Department of Statistics, Oregon State University, Corvallis, Oregon

3. Gladstone Institutes, San Francisco, California, USA

4. Department of Microbiology & Immunology, University of California, San Francisco, San Francisco, California, USA

5. Department of Epidemiology & Biostatistics, Institute for Human Genetics, and Institute for Computational Health Sciences, University of California, San Francisco, San Francisco, California, USA

Abstract

IBD patients harbor distinct microbial communities with functional capabilities different from those seen with healthy people. But is this cause or effect? Answering this question requires data on changes in gut microbial communities leading to disease onset. By performing weekly metagenomic sequencing and mixed-effects modeling on an established mouse model of IBD, we identified several functional pathways encoded by the gut microbiome that covary with host immune status. These pathways are novel early biomarkers that may either enable microbes to live inside an inflamed gut or contribute to immune activation in IBD mice. Future work will validate the potential roles of these microbial pathways in host-microbe interactions and human disease. This study was novel in its longitudinal design and focus on microbial pathways, which provided new mechanistic insights into the role of gut microbes in IBD development.

Funder

NIH/NIAID

Publisher

American Society for Microbiology

Subject

Computer Science Applications,Genetics,Molecular Biology,Modeling and Simulation,Ecology, Evolution, Behavior and Systematics,Biochemistry,Physiology,Microbiology

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