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The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal
BACKGROUND: Bifidobacteria are commensal microbes of the mammalian gastrointestinal tract. In this study, we aimed to identify the intestinal colonization mechanisms and key metabolic pathways implemented by Bifidobacterium dentium. RESULTS: B. dentium displayed acid resistance, with high viability...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145834/ https://www.ncbi.nlm.nih.gov/pubmed/34030655 http://dx.doi.org/10.1186/s12866-021-02166-6 |
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author | Engevik, Melinda A. Danhof, Heather A. Hall, Anne Engevik, Kristen A. Horvath, Thomas D. Haidacher, Sigmund J. Hoch, Kathleen M. Endres, Bradley T. Bajaj, Meghna Garey, Kevin W. Britton, Robert A. Spinler, Jennifer K. Haag, Anthony M. Versalovic, James |
author_facet | Engevik, Melinda A. Danhof, Heather A. Hall, Anne Engevik, Kristen A. Horvath, Thomas D. Haidacher, Sigmund J. Hoch, Kathleen M. Endres, Bradley T. Bajaj, Meghna Garey, Kevin W. Britton, Robert A. Spinler, Jennifer K. Haag, Anthony M. Versalovic, James |
author_sort | Engevik, Melinda A. |
collection | PubMed |
description | BACKGROUND: Bifidobacteria are commensal microbes of the mammalian gastrointestinal tract. In this study, we aimed to identify the intestinal colonization mechanisms and key metabolic pathways implemented by Bifidobacterium dentium. RESULTS: B. dentium displayed acid resistance, with high viability over a pH range from 4 to 7; findings that correlated to the expression of Na+/H+ antiporters within the B. dentium genome. B. dentium was found to adhere to human MUC2+ mucus and harbor mucin-binding proteins. Using microbial phenotyping microarrays and fully-defined media, we demonstrated that in the absence of glucose, B. dentium could metabolize a variety of nutrient sources. Many of these nutrient sources were plant-based, suggesting that B. dentium can consume dietary substances. In contrast to other bifidobacteria, B. dentium was largely unable to grow on compounds found in human mucus; a finding that was supported by its glycosyl hydrolase (GH) profile. Of the proteins identified in B. dentium by proteomic analysis, a large cohort of proteins were associated with diverse metabolic pathways, indicating metabolic plasticity which supports colonization of the dynamic gastrointestinal environment. CONCLUSIONS: Taken together, we conclude that B. dentium is well adapted for commensalism in the gastrointestinal tract. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02166-6. |
format | Online Article Text |
id | pubmed-8145834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81458342021-05-25 The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal Engevik, Melinda A. Danhof, Heather A. Hall, Anne Engevik, Kristen A. Horvath, Thomas D. Haidacher, Sigmund J. Hoch, Kathleen M. Endres, Bradley T. Bajaj, Meghna Garey, Kevin W. Britton, Robert A. Spinler, Jennifer K. Haag, Anthony M. Versalovic, James BMC Microbiol Research Article BACKGROUND: Bifidobacteria are commensal microbes of the mammalian gastrointestinal tract. In this study, we aimed to identify the intestinal colonization mechanisms and key metabolic pathways implemented by Bifidobacterium dentium. RESULTS: B. dentium displayed acid resistance, with high viability over a pH range from 4 to 7; findings that correlated to the expression of Na+/H+ antiporters within the B. dentium genome. B. dentium was found to adhere to human MUC2+ mucus and harbor mucin-binding proteins. Using microbial phenotyping microarrays and fully-defined media, we demonstrated that in the absence of glucose, B. dentium could metabolize a variety of nutrient sources. Many of these nutrient sources were plant-based, suggesting that B. dentium can consume dietary substances. In contrast to other bifidobacteria, B. dentium was largely unable to grow on compounds found in human mucus; a finding that was supported by its glycosyl hydrolase (GH) profile. Of the proteins identified in B. dentium by proteomic analysis, a large cohort of proteins were associated with diverse metabolic pathways, indicating metabolic plasticity which supports colonization of the dynamic gastrointestinal environment. CONCLUSIONS: Taken together, we conclude that B. dentium is well adapted for commensalism in the gastrointestinal tract. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02166-6. BioMed Central 2021-05-24 /pmc/articles/PMC8145834/ /pubmed/34030655 http://dx.doi.org/10.1186/s12866-021-02166-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Engevik, Melinda A. Danhof, Heather A. Hall, Anne Engevik, Kristen A. Horvath, Thomas D. Haidacher, Sigmund J. Hoch, Kathleen M. Endres, Bradley T. Bajaj, Meghna Garey, Kevin W. Britton, Robert A. Spinler, Jennifer K. Haag, Anthony M. Versalovic, James The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal |
title | The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal |
title_full | The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal |
title_fullStr | The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal |
title_full_unstemmed | The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal |
title_short | The metabolic profile of Bifidobacterium dentium reflects its status as a human gut commensal |
title_sort | metabolic profile of bifidobacterium dentium reflects its status as a human gut commensal |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145834/ https://www.ncbi.nlm.nih.gov/pubmed/34030655 http://dx.doi.org/10.1186/s12866-021-02166-6 |
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