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A dietary carbohydrate - gut Parasutterella - human fatty acid biosynthesis metabolic axis in obesity and type 2 diabetes.
Henneke, Lea; Schlicht, Kristina; Andreani, Nadia A; Hollstein, Tim; Demetrowitsch, Tobias; Knappe, Carina; Hartmann, Katharina; Jensen-Kroll, Julia; Rohmann, Nathalie; Pohlschneider, Daniela; Geisler, Corinna; Schulte, Dominik M; Settgast, Ute; Türk, Kathrin; Zimmermann, Johannes; Kaleta, Christoph; Baines, John F; Shearer, Jane; Shah, Shrushti; Shen-Tu, Grace; Schwarz, Karin; Franke, Andre; Schreiber, Stefan; Laudes, Matthias.
Afiliación
  • Henneke L; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Schlicht K; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Andreani NA; Section of Evolutionary Medicine, Institute for Experimental Medicine University of Kiel, Kiel, Germany.
  • Hollstein T; Guest group for evolutionary medicine Max-Planck-Institute of Evolutionary Biology, Plön, Germany.
  • Demetrowitsch T; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Knappe C; Division of Food Technology, Department of Human Nutrition, University of Kiel, Kiel, Germany.
  • Hartmann K; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Jensen-Kroll J; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Rohmann N; Division of Food Technology, Department of Human Nutrition, University of Kiel, Kiel, Germany.
  • Pohlschneider D; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Geisler C; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Schulte DM; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Settgast U; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Türk K; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Zimmermann J; Institute of Diabetes and Clinical Metabolic Research, University of Kiel, Kiel, Germany.
  • Kaleta C; Research Group Medical System Biology, Institute of Experimental Medicine, University of Kiel, Kiel, Germany.
  • Baines JF; Research Group Medical System Biology, Institute of Experimental Medicine, University of Kiel, Kiel, Germany.
  • Shearer J; Section of Evolutionary Medicine, Institute for Experimental Medicine University of Kiel, Kiel, Germany.
  • Shah S; Guest group for evolutionary medicine Max-Planck-Institute of Evolutionary Biology, Plön, Germany.
  • Shen-Tu G; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, Faculty Kinesiology, University of Calgary, Calgary, Alberta, Canada.
  • Schwarz K; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, Faculty Kinesiology, University of Calgary, Calgary, Alberta, Canada.
  • Franke A; Alberta's Tomorrow Project, Cancer Control Alberta, Alberta Health Services, Edmonton, AB, Canada.
  • Schreiber S; Division of Food Technology, Department of Human Nutrition, University of Kiel, Kiel, Germany.
  • Laudes M; Institute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Gut Microbes ; 14(1): 2057778, 2022.
Article en En | MEDLINE | ID: mdl-35435797
ABSTRACT
Recent rodent microbiome experiments suggest that besides Akkermansia, Parasutterella sp. are important in type 2 diabetes and obesity development. In the present translational human study, we aimed to characterize Parasutterella in our European cross-sectional FoCus cohort (n = 1,544) followed by validation of the major results in an independent Canadian cohort (n = 438). In addition, we examined Parasutterella abundance in response to a weight loss intervention (n = 55). Parasutterella was positively associated with BMI and type 2 diabetes independently of the reduced microbiome α/ß diversity and low-grade inflammation commonly found in obesity. Nutritional analysis revealed a positive association with the dietary intake of carbohydrates but not with fat or protein consumption. Out of 126 serum metabolites differentially detectable by untargeted HPLC-based MS-metabolomics, L-cysteine showed the strongest reduction in subjects with high Parasutterella abundance. This is of interest, since Parasutterella is a known high L-cysteine consumer and L-cysteine is known to improve blood glucose levels in rodents. Furthermore, metabolic network enrichment analysis identified an association of high Parasutterella abundance with the activation of the human fatty acid biosynthesis pathway suggesting a mechanism for body weight gain. This is supported by a significant reduction of the Parasutterella abundance during our weight loss intervention. Together, these data indicate a role for Parasutterella in human type 2 diabetes and obesity, whereby the link to L-cysteine might be relevant in type 2 diabetes development and the link to the fatty acid biosynthesis pathway for body weight gain in response to a carbohydrate-rich diet in obesity development.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Diabetes Mellitus Tipo 2 / Microbioma Gastrointestinal Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Gut Microbes Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Asunto principal: Diabetes Mellitus Tipo 2 / Microbioma Gastrointestinal Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Gut Microbes Año: 2022 Tipo del documento: Article País de afiliación: Alemania