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Gut Microbial Structural Variations as Determinants of Human Bile Acid Metabolism

46 Pages Posted: 11 Mar 2021 Publication Status: Review Complete

See all articles by Daoming Wang

Daoming Wang

University of Groningen - Department of Genetics

Marwah Doestzada

University of Groningen - Department of Genetics

Lianmin Chen

University of Groningen - Department of Genetics

Sergio Andreu-Sánchez

University of Groningen - Department of Genetics

Inge van den Munckhof

Radboud University Nijmegen - Radboud University Medical Center

Hannah Augustijn

University of Groningen - Department of Genetics

Martijn Koehorst

Radboud University Nijmegen - Radboud University Medical Center

Vincent W. Bloks

University of Groningen - Department of Pediatrics

Niels Riksen

Radboud University Nijmegen - Radboud Institute for Molecular Life Sciences (RIMLS)

Joost H.W. Rutten

Radboud University Medical Center - Department of Internal Medicine

Mihai G. Netea

Radboud University Nijmegen - Radboud Center for Infectious Diseases (RCI); Radboud University Nijmegen - Department of Internal Medicine

Alexandra Zhernakova

University of Groningen - Department of Genetics

Folkert Kuipers

University of Groningen - Department of Pediatrics

Jingyuan Fu

University of Groningen - Department of Genetics

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Multiple version iconThere are 2 versions of this paper

Abstract

Bile acids (BAs) facilitate intestinal fat absorption and act as important signaling molecules in host‒gut microbiota crosstalk. BA-metabolizing pathways in the microbial community have been identified, but how the highly variable genomes of gut bacteria interact with host BA metabolism remains largely unknown. We characterized 8,282 structural variants (SVs) of 55 bacterial species in the gut microbiomes of 1,437 individuals from two Dutch cohorts and performed a systematic association study with 39 plasma BA parameters. Both variations in SV-based continuous genetic makeup and discrete subspecies showed correlations with BA metabolism. Metagenome-wide association analysis identified 797 replicable associations between bacterial SVs and BAs and SV regulators that mediate the effects of lifestyle factors on BA metabolism. This is the first large-scale microbial genetic association analysis to demonstrate the impact of bacterial SVs on human BA composition, and highlights the potential of targeting gut microbiota to regulate BA metabolism through lifestyle intervention.

Keywords: Human gut microbiome, bile acid metabolism, bacterial genetics, structural variation

Suggested Citation

Wang, Daoming and Doestzada, Marwah and Chen, Lianmin and Andreu-Sánchez, Sergio and van den Munckhof, Inge and Augustijn, Hannah and Koehorst, Martijn and Bloks, Vincent W. and Riksen, Niels and Rutten, Joost H.W. and Netea, Mihai G. and Zhernakova, Alexandra and Kuipers, Folkert and Fu, Jingyuan, Gut Microbial Structural Variations as Determinants of Human Bile Acid Metabolism. Available at SSRN: https://ssrn.com/abstract=3802853 or http://dx.doi.org/10.2139/ssrn.3802853
This version of the paper has not been formally peer reviewed.

Daoming Wang

University of Groningen - Department of Genetics ( email )

Hanzeplein 1, 9700 RB
Groningen
Netherlands

Marwah Doestzada

University of Groningen - Department of Genetics ( email )

Hanzeplein 1, 9700 RB
Groningen
Netherlands

Lianmin Chen

University of Groningen - Department of Genetics ( email )

Hanzeplein 1
Groningen, 9713
Netherlands

Sergio Andreu-Sánchez

University of Groningen - Department of Genetics ( email )

Hanzeplein 1, 9700 RB
Groningen
Netherlands

Inge Van den Munckhof

Radboud University Nijmegen - Radboud University Medical Center

Hannah Augustijn

University of Groningen - Department of Genetics ( email )

Hanzeplein 1, 9700 RB
Groningen
Netherlands

Martijn Koehorst

Radboud University Nijmegen - Radboud University Medical Center

Geert Grooteplein Zuid 10
Nijmegen
Netherlands

Vincent W. Bloks

University of Groningen - Department of Pediatrics

P.O. Box 800
9700 AH Groningen, Groningen 9700 AV
Netherlands

Niels Riksen

Radboud University Nijmegen - Radboud Institute for Molecular Life Sciences (RIMLS) ( email )

6525 GA Nijmegen
Netherlands

Joost H.W. Rutten

Radboud University Medical Center - Department of Internal Medicine

Geert Grooteplein Zuid 10
Nijmegen
Netherlands

Mihai G. Netea

Radboud University Nijmegen - Radboud Center for Infectious Diseases (RCI)

Nijmegen
Netherlands

Radboud University Nijmegen - Department of Internal Medicine ( email )

Nijmegen
Netherlands

Alexandra Zhernakova

University of Groningen - Department of Genetics ( email )

Hanzeplein 1, 9700 RB
Groningen
Netherlands

Folkert Kuipers

University of Groningen - Department of Pediatrics ( email )

P.O. Box 800
9700 AH Groningen, Groningen 9700 AV
Netherlands

Jingyuan Fu (Contact Author)

University of Groningen - Department of Genetics ( email )

Netherlands

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