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Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice

Industrialization has transformed the gut microbiota, reducing the prevalence of Prevotella relative to Bacteroides. Here, we isolate Bacteroides and Prevotella strains from the microbiota of Hadza hunter-gatherers of Tanzania, a population with high levels of Prevotella. We demonstrate that plant-d...

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Autores principales: Gellman, Rebecca H, Olm, Matthew R, Terrapon, Nicolas, Enam, Fatima, Higginbottom, Steven K, Sonnenburg, Justin L, Sonnenburg, Erica D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028851/
https://www.ncbi.nlm.nih.gov/pubmed/36945614
http://dx.doi.org/10.1101/2023.03.08.531063
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author Gellman, Rebecca H
Olm, Matthew R
Terrapon, Nicolas
Enam, Fatima
Higginbottom, Steven K
Sonnenburg, Justin L
Sonnenburg, Erica D
author_facet Gellman, Rebecca H
Olm, Matthew R
Terrapon, Nicolas
Enam, Fatima
Higginbottom, Steven K
Sonnenburg, Justin L
Sonnenburg, Erica D
author_sort Gellman, Rebecca H
collection PubMed
description Industrialization has transformed the gut microbiota, reducing the prevalence of Prevotella relative to Bacteroides. Here, we isolate Bacteroides and Prevotella strains from the microbiota of Hadza hunter-gatherers of Tanzania, a population with high levels of Prevotella. We demonstrate that plant-derived microbiota-accessible carbohydrates (MACs) are required for persistence of Prevotella copri but not Bacteroides thetaiotaomicron in vivo. Differences in carbohydrate metabolism gene content, expression, and in vitro growth reveal that Hadza Prevotella strains specialize in degrading plant carbohydrates, while Hadza Bacteroides isolates use both plant and host-derived carbohydrates, a difference mirrored in Bacteroides from non-Hadza populations. When competing directly, P. copri requires plant-derived MACs to maintain colonization in the presence of B. thetaiotaomicron, as a no MAC diet eliminates P. copri colonization. Prevotella’s reliance on plant-derived MACs and Bacteroides’ ability to use host mucus carbohydrates could explain the reduced prevalence of Prevotella in populations consuming a low-MAC, industrialized diet.
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spelling pubmed-100288512023-03-22 Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice Gellman, Rebecca H Olm, Matthew R Terrapon, Nicolas Enam, Fatima Higginbottom, Steven K Sonnenburg, Justin L Sonnenburg, Erica D bioRxiv Article Industrialization has transformed the gut microbiota, reducing the prevalence of Prevotella relative to Bacteroides. Here, we isolate Bacteroides and Prevotella strains from the microbiota of Hadza hunter-gatherers of Tanzania, a population with high levels of Prevotella. We demonstrate that plant-derived microbiota-accessible carbohydrates (MACs) are required for persistence of Prevotella copri but not Bacteroides thetaiotaomicron in vivo. Differences in carbohydrate metabolism gene content, expression, and in vitro growth reveal that Hadza Prevotella strains specialize in degrading plant carbohydrates, while Hadza Bacteroides isolates use both plant and host-derived carbohydrates, a difference mirrored in Bacteroides from non-Hadza populations. When competing directly, P. copri requires plant-derived MACs to maintain colonization in the presence of B. thetaiotaomicron, as a no MAC diet eliminates P. copri colonization. Prevotella’s reliance on plant-derived MACs and Bacteroides’ ability to use host mucus carbohydrates could explain the reduced prevalence of Prevotella in populations consuming a low-MAC, industrialized diet. Cold Spring Harbor Laboratory 2023-03-09 /pmc/articles/PMC10028851/ /pubmed/36945614 http://dx.doi.org/10.1101/2023.03.08.531063 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Gellman, Rebecca H
Olm, Matthew R
Terrapon, Nicolas
Enam, Fatima
Higginbottom, Steven K
Sonnenburg, Justin L
Sonnenburg, Erica D
Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice
title Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice
title_full Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice
title_fullStr Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice
title_full_unstemmed Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice
title_short Hadza Prevotella Require Diet-derived Microbiota Accessible Carbohydrates to Persist in Mice
title_sort hadza prevotella require diet-derived microbiota accessible carbohydrates to persist in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028851/
https://www.ncbi.nlm.nih.gov/pubmed/36945614
http://dx.doi.org/10.1101/2023.03.08.531063
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