| Literature DB >> 31071294 |
Eric M Brown1, Xiaobo Ke2, Daniel Hitchcock3, Sarah Jeanfavre3, Julian Avila-Pacheco3, Toru Nakata3, Timothy D Arthur3, Nadine Fornelos3, Cortney Heim4, Eric A Franzosa5, Nicki Watson6, Curtis Huttenhower5, Henry J Haiser4, Glen Dillow4, Daniel B Graham3, B Brett Finlay7, Aleksandar D Kostic8, Jeffrey A Porter4, Hera Vlamakis1, Clary B Clish3, Ramnik J Xavier9.
Abstract
Sphingolipids are structural membrane components and important eukaryotic signaling molecules. Sphingolipids regulate inflammation and immunity and were recently identified as the most differentially abundant metabolite in stool from inflammatory bowel disease (IBD) patients. Commensal bacteria from the Bacteroidetes phylum also produce sphingolipids, but the impact of these metabolites on host pathways is largely uncharacterized. To determine whether bacterial sphingolipids modulate intestinal health, we colonized germ-free mice with a sphingolipid-deficient Bacteroides thetaiotaomicron strain. A lack of Bacteroides-derived sphingolipids resulted in intestinal inflammation and altered host ceramide pools in mice. Using lipidomic analysis, we described a sphingolipid biosynthesis pathway and revealed a variety of Bacteroides-derived sphingolipids including ceramide phosphoinositol and deoxy-sphingolipids. Annotating Bacteroides sphingolipids in an IBD metabolomic dataset revealed lower abundances in IBD and negative correlations with inflammation and host sphingolipid production. These data highlight the role of bacterial sphingolipids in maintaining homeostasis and symbiosis in the gut.Entities:
Keywords: Bacteroides; inflammation; inflammatory bowel disease; innate immunity; metabolism; microbiome; sphingolipids
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Year: 2019 PMID: 31071294 PMCID: PMC6544385 DOI: 10.1016/j.chom.2019.04.002
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023