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Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations

The human gut teems with a diverse ecosystem of microbes, yet non-bacterial portions of that community are overlooked in studies of metabolic diseases firmly linked to gut bacteria. Type 2 diabetes mellitus (T2D) associates with compositional shifts in the gut bacterial microbiome and fungal mycobio...

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Autores principales: Van Syoc, Emily, Nixon, Michelle Pistner, Silverman, Justin D., Luo, Yuhong, Gonzalez, Frank J., Elbere, Ilze, Klovins, Janis, Patterson, Andrew D., Rogers, Connie J., Ganda, Erika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312434/
https://www.ncbi.nlm.nih.gov/pubmed/37398234
http://dx.doi.org/10.1101/2023.05.25.542255
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author Van Syoc, Emily
Nixon, Michelle Pistner
Silverman, Justin D.
Luo, Yuhong
Gonzalez, Frank J.
Elbere, Ilze
Klovins, Janis
Patterson, Andrew D.
Rogers, Connie J.
Ganda, Erika
author_facet Van Syoc, Emily
Nixon, Michelle Pistner
Silverman, Justin D.
Luo, Yuhong
Gonzalez, Frank J.
Elbere, Ilze
Klovins, Janis
Patterson, Andrew D.
Rogers, Connie J.
Ganda, Erika
author_sort Van Syoc, Emily
collection PubMed
description The human gut teems with a diverse ecosystem of microbes, yet non-bacterial portions of that community are overlooked in studies of metabolic diseases firmly linked to gut bacteria. Type 2 diabetes mellitus (T2D) associates with compositional shifts in the gut bacterial microbiome and fungal mycobiome, but whether T2D and/or pharmaceutical treatments underpin the community change is unresolved. To differentiate these effects, we curated a gut mycobiome cohort to-date spanning 1,000 human samples across 5 countries and a murine experimental model. We use Bayesian multinomial logistic normal models to show that metformin and T2D both associate with shifts in the relative abundance of distinct gut fungi. T2D associates with shifts in the Saccharomycetes and Sordariomycetes fungal classes, while the genera Fusarium and Tetrapisipora most consistently associate with metformin treatment. We confirmed the impact of metformin on individual gut fungi by administering metformin to healthy mice. Thus, metformin and T2D account for subtle, but significant and distinct variation in the gut mycobiome across human populations. This work highlights for the first time that oral pharmaceuticals can confound associations of gut fungi with T2D and warrants the need to consider pharmaceutical interventions in investigations of linkages between metabolic diseases and gut microbial inhabitants.
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spelling pubmed-103124342023-07-01 Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations Van Syoc, Emily Nixon, Michelle Pistner Silverman, Justin D. Luo, Yuhong Gonzalez, Frank J. Elbere, Ilze Klovins, Janis Patterson, Andrew D. Rogers, Connie J. Ganda, Erika bioRxiv Article The human gut teems with a diverse ecosystem of microbes, yet non-bacterial portions of that community are overlooked in studies of metabolic diseases firmly linked to gut bacteria. Type 2 diabetes mellitus (T2D) associates with compositional shifts in the gut bacterial microbiome and fungal mycobiome, but whether T2D and/or pharmaceutical treatments underpin the community change is unresolved. To differentiate these effects, we curated a gut mycobiome cohort to-date spanning 1,000 human samples across 5 countries and a murine experimental model. We use Bayesian multinomial logistic normal models to show that metformin and T2D both associate with shifts in the relative abundance of distinct gut fungi. T2D associates with shifts in the Saccharomycetes and Sordariomycetes fungal classes, while the genera Fusarium and Tetrapisipora most consistently associate with metformin treatment. We confirmed the impact of metformin on individual gut fungi by administering metformin to healthy mice. Thus, metformin and T2D account for subtle, but significant and distinct variation in the gut mycobiome across human populations. This work highlights for the first time that oral pharmaceuticals can confound associations of gut fungi with T2D and warrants the need to consider pharmaceutical interventions in investigations of linkages between metabolic diseases and gut microbial inhabitants. Cold Spring Harbor Laboratory 2023-11-03 /pmc/articles/PMC10312434/ /pubmed/37398234 http://dx.doi.org/10.1101/2023.05.25.542255 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Van Syoc, Emily
Nixon, Michelle Pistner
Silverman, Justin D.
Luo, Yuhong
Gonzalez, Frank J.
Elbere, Ilze
Klovins, Janis
Patterson, Andrew D.
Rogers, Connie J.
Ganda, Erika
Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations
title Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations
title_full Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations
title_fullStr Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations
title_full_unstemmed Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations
title_short Changes in the Type 2 diabetes gut mycobiome associate with metformin treatment across populations
title_sort changes in the type 2 diabetes gut mycobiome associate with metformin treatment across populations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312434/
https://www.ncbi.nlm.nih.gov/pubmed/37398234
http://dx.doi.org/10.1101/2023.05.25.542255
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