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Growth effects of N-acylethanolamines on gut bacteria reflect altered bacterial abundances in inflammatory bowel disease.
Fornelos, Nadine; Franzosa, Eric A; Bishai, Jason; Annand, John W; Oka, Akihiko; Lloyd-Price, Jason; Arthur, Timothy D; Garner, Ashley; Avila-Pacheco, Julian; Haiser, Henry J; Tolonen, Andrew C; Porter, Jeffrey A; Clish, Clary B; Sartor, R Balfour; Huttenhower, Curtis; Vlamakis, Hera; Xavier, Ramnik J.
Afiliação
  • Fornelos N; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Franzosa EA; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Bishai J; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Annand JW; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Oka A; Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research Inc., Cambridge, MA, USA.
  • Lloyd-Price J; Departments of Medicine, Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Arthur TD; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Garner A; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Avila-Pacheco J; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Haiser HJ; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Tolonen AC; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Porter JA; Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research Inc., Cambridge, MA, USA.
  • Clish CB; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Sartor RB; Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research Inc., Cambridge, MA, USA.
  • Huttenhower C; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Vlamakis H; Departments of Medicine, Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Xavier RJ; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nat Microbiol ; 5(3): 486-497, 2020 03.
Article em En | MEDLINE | ID: mdl-31959971
ABSTRACT
Inflammatory bowel diseases (IBD) are associated with alterations in gut microbial abundances and lumenal metabolite concentrations, but the effects of specific metabolites on the gut microbiota in health and disease remain largely unknown. Here, we analysed the influences of metabolites that are differentially abundant in IBD on the growth and physiology of gut bacteria that are also differentially abundant in IBD. We found that N-acylethanolamines (NAEs), a class of endogenously produced signalling lipids elevated in the stool of IBD patients and a T-cell transfer model of colitis, stimulated growth of species over-represented in IBD and inhibited that of species depleted in IBD in vitro. Using metagenomic sequencing, we recapitulated the effects of NAEs in complex microbial communities ex vivo, with Proteobacteria blooming and Bacteroidetes declining in the presence of NAEs. Metatranscriptomic analysis of the same communities identified components of the respiratory chain as important for the metabolism of NAEs, and this was verified using a mutant deficient for respiratory complex I. In this study, we identified NAEs as a class of metabolites that are elevated in IBD and have the potential to shift gut microbiota towards an IBD-like composition.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bactérias / Doenças Inflamatórias Intestinais / Etanolaminas / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bactérias / Doenças Inflamatórias Intestinais / Etanolaminas / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2020 Tipo de documento: Article