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Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements

Muscle builders frequently consume protein supplements, but little is known about their effect on the gut microbiota. This study compared the gut microbiome and metabolome of self-identified muscle builders who did or did not report consuming a protein supplement. Twenty-two participants (14 males a...

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Autores principales: Byerley, Lauri O., Gallivan, Karyn M., Christopher, Courtney J., Taylor, Christopher M., Luo, Meng, Dowd, Scot E., Davis, Gregory M., Castro, Hector F., Campagna, Shawn R., Ondrak, Kristin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839395/
https://www.ncbi.nlm.nih.gov/pubmed/35276896
http://dx.doi.org/10.3390/nu14030533
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author Byerley, Lauri O.
Gallivan, Karyn M.
Christopher, Courtney J.
Taylor, Christopher M.
Luo, Meng
Dowd, Scot E.
Davis, Gregory M.
Castro, Hector F.
Campagna, Shawn R.
Ondrak, Kristin S.
author_facet Byerley, Lauri O.
Gallivan, Karyn M.
Christopher, Courtney J.
Taylor, Christopher M.
Luo, Meng
Dowd, Scot E.
Davis, Gregory M.
Castro, Hector F.
Campagna, Shawn R.
Ondrak, Kristin S.
author_sort Byerley, Lauri O.
collection PubMed
description Muscle builders frequently consume protein supplements, but little is known about their effect on the gut microbiota. This study compared the gut microbiome and metabolome of self-identified muscle builders who did or did not report consuming a protein supplement. Twenty-two participants (14 males and 8 females) consumed a protein supplement (PS), and seventeen participants (12 males and 5 females) did not (No PS). Participants provided a fecal sample and completed a 24-h food recall (ASA24). The PS group consumed significantly more protein (118 ± 12 g No PS vs. 169 ± 18 g PS, p = 0.02). Fecal metabolome and microbiome were analyzed by using untargeted metabolomics and 16S rRNA gene sequencing, respectively. Metabolomic analysis identified distinct metabolic profiles driven by allantoin (VIP score = 2.85, PS 2.3-fold higher), a catabolic product of uric acid. High-protein diets contain large quantities of purines, which gut microbes degrade to uric acid and then allantoin. The bacteria order Lactobacillales was higher in the PS group (22.6 ± 49 No PS vs. 136.5 ± 38.1, PS (p = 0.007)), and this bacteria family facilitates purine absorption and uric acid decomposition. Bacterial genes associated with nucleotide metabolism pathways (p < 0.001) were more highly expressed in the No PS group. Both fecal metagenomic and metabolomic analyses revealed that the PS group’s higher protein intake impacted nitrogen metabolism, specifically altering nucleotide degradation.
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spelling pubmed-88393952022-02-13 Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements Byerley, Lauri O. Gallivan, Karyn M. Christopher, Courtney J. Taylor, Christopher M. Luo, Meng Dowd, Scot E. Davis, Gregory M. Castro, Hector F. Campagna, Shawn R. Ondrak, Kristin S. Nutrients Article Muscle builders frequently consume protein supplements, but little is known about their effect on the gut microbiota. This study compared the gut microbiome and metabolome of self-identified muscle builders who did or did not report consuming a protein supplement. Twenty-two participants (14 males and 8 females) consumed a protein supplement (PS), and seventeen participants (12 males and 5 females) did not (No PS). Participants provided a fecal sample and completed a 24-h food recall (ASA24). The PS group consumed significantly more protein (118 ± 12 g No PS vs. 169 ± 18 g PS, p = 0.02). Fecal metabolome and microbiome were analyzed by using untargeted metabolomics and 16S rRNA gene sequencing, respectively. Metabolomic analysis identified distinct metabolic profiles driven by allantoin (VIP score = 2.85, PS 2.3-fold higher), a catabolic product of uric acid. High-protein diets contain large quantities of purines, which gut microbes degrade to uric acid and then allantoin. The bacteria order Lactobacillales was higher in the PS group (22.6 ± 49 No PS vs. 136.5 ± 38.1, PS (p = 0.007)), and this bacteria family facilitates purine absorption and uric acid decomposition. Bacterial genes associated with nucleotide metabolism pathways (p < 0.001) were more highly expressed in the No PS group. Both fecal metagenomic and metabolomic analyses revealed that the PS group’s higher protein intake impacted nitrogen metabolism, specifically altering nucleotide degradation. MDPI 2022-01-26 /pmc/articles/PMC8839395/ /pubmed/35276896 http://dx.doi.org/10.3390/nu14030533 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Byerley, Lauri O.
Gallivan, Karyn M.
Christopher, Courtney J.
Taylor, Christopher M.
Luo, Meng
Dowd, Scot E.
Davis, Gregory M.
Castro, Hector F.
Campagna, Shawn R.
Ondrak, Kristin S.
Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements
title Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements
title_full Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements
title_fullStr Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements
title_full_unstemmed Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements
title_short Gut Microbiome and Metabolome Variations in Self-Identified Muscle Builders Who Report Using Protein Supplements
title_sort gut microbiome and metabolome variations in self-identified muscle builders who report using protein supplements
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839395/
https://www.ncbi.nlm.nih.gov/pubmed/35276896
http://dx.doi.org/10.3390/nu14030533
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