Longitudinal Multi-omics Reveals Subset-Specific Mechanisms Underlying Irritable Bowel Syndrome.
Animals
Bile Acids and Salts
/ metabolism
Biopsy
Butyrates
/ metabolism
Chromatography, Liquid
Cross-Sectional Studies
Epigenomics
Feces
/ microbiology
Female
Gastrointestinal Microbiome
/ genetics
Gene Expression Regulation
/ genetics
Host Microbial Interactions
/ genetics
Humans
Hypoxanthine
/ metabolism
Irritable Bowel Syndrome
/ genetics
Longitudinal Studies
Male
Metabolome
/ physiology
Mice
Observational Studies as Topic
Prospective Studies
Purines
/ metabolism
Software
Tandem Mass Spectrometry
Transcriptome
/ genetics
bile acids
diet
functional bowel disorders
nucleosides
physiology
secretion
short chain fatti acids
symptom severity
Journal
Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066
Informations de publication
Date de publication:
17 09 2020
17 09 2020
Historique:
received:
05
11
2019
revised:
25
05
2020
accepted:
31
07
2020
pubmed:
12
9
2020
medline:
20
5
2021
entrez:
11
9
2020
Statut:
ppublish
Résumé
The gut microbiome has been implicated in multiple human chronic gastrointestinal (GI) disorders. Determining its mechanistic role in disease has been difficult due to apparent disconnects between animal and human studies and lack of an integrated multi-omics view of disease-specific physiological changes. We integrated longitudinal multi-omics data from the gut microbiome, metabolome, host epigenome, and transcriptome in the context of irritable bowel syndrome (IBS) host physiology. We identified IBS subtype-specific and symptom-related variation in microbial composition and function. A subset of identified changes in microbial metabolites correspond to host physiological mechanisms that are relevant to IBS. By integrating multiple data layers, we identified purine metabolism as a novel host-microbial metabolic pathway in IBS with translational potential. Our study highlights the importance of longitudinal sampling and integrating complementary multi-omics data to identify functional mechanisms that can serve as therapeutic targets in a comprehensive treatment strategy for chronic GI diseases. VIDEO ABSTRACT.
Identifiants
pubmed: 32916129
pii: S0092-8674(20)30998-3
doi: 10.1016/j.cell.2020.08.007
pmc: PMC8109273
mid: NIHMS1695469
pii:
doi:
Substances chimiques
Bile Acids and Salts
0
Butyrates
0
Purines
0
Hypoxanthine
2TN51YD919
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1460-1473.e17Subventions
Organisme : NIDDK NIH HHS
ID : P30 DK084567
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK114007
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM128716
Pays : United States
Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Interests P.C.K. is on the Advisory Board of Novome Biotechnologies and is an ad hoc consultant for Pendulum Therapeutics, IP group, and Otsuka Pharmaceuticals. P.C.K. holds patent US20170042860A1 for use of tryptamine producing bacteria (“Methods and materials for using Ruminococcus gnavus or Clostridium sporogenes to treat gastrointestinal disorders”), and P.C.K. and Mayo Clinic have a financial interest related to this research. These interests have been reviewed and managed in accordance with Mayo Clinic Conflict-of-Interest policies. D.B.K. serves as CEO of CoreBiome, a company involved in the commercialization of microbiome analysis and a wholly owned subsidiary of OraSure Technologies. These interests have been reviewed and managed by the University of Minnesota in accordance with its Conflict-of-Interest policies.
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