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Microbial community-scale metabolic modelling predicts personalized short-chain fatty acid production profiles in the human gut.
Quinn-Bohmann, Nick; Wilmanski, Tomasz; Sarmiento, Katherine Ramos; Levy, Lisa; Lampe, Johanna W; Gurry, Thomas; Rappaport, Noa; Ostrem, Erin M; Venturelli, Ophelia S; Diener, Christian; Gibbons, Sean M.
Afiliación
  • Quinn-Bohmann N; Institute for Systems Biology, Seattle, WA, USA.
  • Wilmanski T; Molecular Engineering Graduate Program, University of Washington, Seattle, WA, USA.
  • Sarmiento KR; Institute for Systems Biology, Seattle, WA, USA.
  • Levy L; Institute for Systems Biology, Seattle, WA, USA.
  • Lampe JW; Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Gurry T; Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Rappaport N; Pharmaceutical Biochemistry Group, School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
  • Ostrem EM; Myota GmbH, Berlin, Germany.
  • Venturelli OS; Center for Phenomic Health, Buck Institute for Research on Aging, Novato, CA, USA.
  • Diener C; Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA.
  • Gibbons SM; Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, USA.
Nat Microbiol ; 9(7): 1700-1712, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38914826
ABSTRACT
Microbially derived short-chain fatty acids (SCFAs) in the human gut are tightly coupled to host metabolism, immune regulation and integrity of the intestinal epithelium. However, the production of SCFAs can vary widely between individuals consuming the same diet, with lower levels often associated with disease. A systems-scale mechanistic understanding of this heterogeneity is lacking. Here we use a microbial community-scale metabolic modelling (MCMM) approach to predict individual-specific SCFA production profiles to assess the impact of different dietary, prebiotic and probiotic inputs. We evaluate the quantitative accuracy of our MCMMs using in vitro and ex vivo data, plus published human cohort data. We find that MCMM SCFA predictions are significantly associated with blood-derived clinical chemistries, including cardiometabolic and immunological health markers, across a large human cohort. Finally, we demonstrate how MCMMs can be leveraged to design personalized dietary, prebiotic and probiotic interventions aimed at optimizing SCFA production in the gut. Our model represents an approach to direct gut microbiome engineering for precision health and nutrition.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácidos Grasos Volátiles / Microbioma Gastrointestinal Límite: Adult / Humans Idioma: En Revista: Nat Microbiol / Nat. microbiol / Nature microbiology Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácidos Grasos Volátiles / Microbioma Gastrointestinal Límite: Adult / Humans Idioma: En Revista: Nat Microbiol / Nat. microbiol / Nature microbiology Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos