Article (Scientific journals)
Personalized modeling of gut microbiome metabolism throughout the first year of life.
Shaaban, Rola; BUSI, Susheel Bhanu; WILMES, Paul et al.
2024In Communications Medicine, 4 (1), p. 281
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Keywords :
Public Health, Environmental and Occupational Health; Internal Medicine; Epidemiology; Medicine (miscellaneous); Assessment and Diagnosis
Abstract :
[en] [en] BACKGROUND: Early-life exposures including diet, and the gut microbiome have been proposed to predispose infants towards multifactorial diseases later in life. Delivery via Cesarian section disrupts the establishment of the gut microbiome and has been associated with negative long-term outcomes. Here, we hypothesize that Cesarian section delivery alters not only the composition of the developing infant gut microbiome but also its metabolic capabilities. To test this, we developed a metabolic modeling workflow targeting the infant gut microbiome. METHODS: The AGORA2 resource of human microbial genome-scale reconstructions was expanded with a human milk oligosaccharide degradation module. Personalized metabolic modeling of the gut microbiome was performed for a cohort of 20 infants at four time points during the first year of life as well as for 13 maternal gut microbiome samples. RESULTS: Here we show that at the earliest stages, the gut microbiomes of infants delivered through Cesarian section are depleted in their metabolic capabilities compared with vaginal delivery. Various metabolites such as fermentation products, human milk oligosaccharide degradation products, and amino acids are depleted in Cesarian section delivery gut microbiomes. Compared with maternal gut microbiomes, infant gut microbiomes produce less butyrate but more L-lactate and are enriched in the potential to synthesize B-vitamins. CONCLUSIONS: Our simulations elucidate the metabolic capabilities of the infant gut microbiome demonstrating they are altered in Cesarian section delivery at the earliest time points. Our workflow can be readily applied to other cohorts to evaluate the effect of feeding type, or maternal factors such as diet on host-gut microbiome inactions in early life.
[en] Trillions of microorganisms live in the digestive system of humans, with those within the intestine being described as the intestinal microbiome. Intestinal microbes perform important metabolic functions such as digestion of the diet (e.g., breast milk) and production of metabolites such as B-vitamins. Birth via Cesarian section disrupts the establishment of the gut microbiome. Here, we evaluate the effect of birth mode on microbiome metabolic functions during the first year of life. Computational metabolic models were built for a cohort of mothers and infants, with each model representing the individual’s unique microbiome. Microbiomes from infants delivered by Cesarian section had perturbed metabolic functions early in life but became comparable to those in vaginally delivered infants later in life. Moreover, the metabolic functions present in infant gut microbiomes differed from those in maternal gut microbiomes. This information could be a useful starting point for further research to improve the intestinal microbiome of babies born by Cesarian section.
Disciplines :
Microbiology
Author, co-author :
Shaaban, Rola;  Inserm UMRS 1256 NGERE, University of Lorraine, Nancy, France ; Nantes University, Nantes, France
BUSI, Susheel Bhanu  ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine > Systems Ecology > Team Paul WILMES
WILMES, Paul  ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > Systems Ecology
Guéant, Jean-Louis ;  Inserm UMRS 1256 NGERE, University of Lorraine, Nancy, France ; National Center of Inborn Errors of Metabolism, University Regional Hospital Center of Nancy, Nancy, France
Heinken, Almut ;  Inserm UMRS 1256 NGERE, University of Lorraine, Nancy, France. almut-katrin.heinken@univ-lorraine.fr
External co-authors :
yes
Language :
English
Title :
Personalized modeling of gut microbiome metabolism throughout the first year of life.
Publication date :
30 December 2024
Journal title :
Communications Medicine
eISSN :
2730-664X
Publisher :
Springer Nature, England
Volume :
4
Issue :
1
Pages :
281
Peer reviewed :
Peer Reviewed verified by ORBi
FnR Project :
FNR10404839 - LEGeLiS (for Linking Environment - Genome - Lifestyle Strategy) - Linking Environmental Condition To Lifestyle Strategies And To Population-level Genetic Heterogeneity, 2015 (01/12/2015-14/09/2018) - Paul Wilmes
Funders :
Agence Nationale de la Recherche
Funding text :
The present project was funded by a Chaire de professeur junior (CPJ) granted to A.H. by the Agence Nationale de la Recherche (ANR) under the decree 2021-1710. It was also partially financed by the Andr\u00E9 Losch Foundation. It was further supported by an ATTRACT program grant (ATTRACT/A09/03) and CORE program grants (CORE/15/BM/104040 and CORE/C15/SR/10404839) to P.W., all funded by the Luxembourg National Research Fund (FNR). The project also received funding from the European Research Council (ERC) under the European Union\u2019s Horizon 2020 research and innovation program (grant agreement No. 863664).
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