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Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes
The human gut microbiota supplies its host with essential nutrients, including B-vitamins. Using the PubSEED platform, we systematically assessed the genomes of 256 common human gut bacteria for the presence of biosynthesis pathways for eight B-vitamins: biotin, cobalamin, folate, niacin, pantothena...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403557/ https://www.ncbi.nlm.nih.gov/pubmed/25941533 http://dx.doi.org/10.3389/fgene.2015.00148 |
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author | Magnúsdóttir, Stefanía Ravcheev, Dmitry de Crécy-Lagard, Valérie Thiele, Ines |
author_facet | Magnúsdóttir, Stefanía Ravcheev, Dmitry de Crécy-Lagard, Valérie Thiele, Ines |
author_sort | Magnúsdóttir, Stefanía |
collection | PubMed |
description | The human gut microbiota supplies its host with essential nutrients, including B-vitamins. Using the PubSEED platform, we systematically assessed the genomes of 256 common human gut bacteria for the presence of biosynthesis pathways for eight B-vitamins: biotin, cobalamin, folate, niacin, pantothenate, pyridoxine, riboflavin, and thiamin. On the basis of the presence and absence of genome annotations, we predicted that each of the eight vitamins was produced by 40–65% of the 256 human gut microbes. The distribution of synthesis pathways was diverse; some genomes had all eight biosynthesis pathways, whereas others contained no de novo synthesis pathways. We compared our predictions to experimental data from 16 organisms and found 88% of our predictions to be in agreement with published data. In addition, we identified several pairs of organisms whose vitamin synthesis pathway pattern complemented those of other organisms. This analysis suggests that human gut bacteria actively exchange B-vitamins among each other, thereby enabling the survival of organisms that do not synthesize any of these essential cofactors. This result indicates the co-evolution of the gut microbes in the human gut environment. Our work presents the first comprehensive assessment of the B-vitamin synthesis capabilities of the human gut microbiota. We propose that in addition to diet, the gut microbiota is an important source of B-vitamins, and that changes in the gut microbiota composition can severely affect our dietary B-vitamin requirements. |
format | Online Article Text |
id | pubmed-4403557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44035572015-05-04 Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes Magnúsdóttir, Stefanía Ravcheev, Dmitry de Crécy-Lagard, Valérie Thiele, Ines Front Genet Genetics The human gut microbiota supplies its host with essential nutrients, including B-vitamins. Using the PubSEED platform, we systematically assessed the genomes of 256 common human gut bacteria for the presence of biosynthesis pathways for eight B-vitamins: biotin, cobalamin, folate, niacin, pantothenate, pyridoxine, riboflavin, and thiamin. On the basis of the presence and absence of genome annotations, we predicted that each of the eight vitamins was produced by 40–65% of the 256 human gut microbes. The distribution of synthesis pathways was diverse; some genomes had all eight biosynthesis pathways, whereas others contained no de novo synthesis pathways. We compared our predictions to experimental data from 16 organisms and found 88% of our predictions to be in agreement with published data. In addition, we identified several pairs of organisms whose vitamin synthesis pathway pattern complemented those of other organisms. This analysis suggests that human gut bacteria actively exchange B-vitamins among each other, thereby enabling the survival of organisms that do not synthesize any of these essential cofactors. This result indicates the co-evolution of the gut microbes in the human gut environment. Our work presents the first comprehensive assessment of the B-vitamin synthesis capabilities of the human gut microbiota. We propose that in addition to diet, the gut microbiota is an important source of B-vitamins, and that changes in the gut microbiota composition can severely affect our dietary B-vitamin requirements. Frontiers Media S.A. 2015-04-20 /pmc/articles/PMC4403557/ /pubmed/25941533 http://dx.doi.org/10.3389/fgene.2015.00148 Text en Copyright © 2015 Magnúsdóttir, Ravcheev, de Crécy-Lagard and Thiele. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Magnúsdóttir, Stefanía Ravcheev, Dmitry de Crécy-Lagard, Valérie Thiele, Ines Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes |
title | Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes |
title_full | Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes |
title_fullStr | Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes |
title_full_unstemmed | Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes |
title_short | Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes |
title_sort | systematic genome assessment of b-vitamin biosynthesis suggests co-operation among gut microbes |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403557/ https://www.ncbi.nlm.nih.gov/pubmed/25941533 http://dx.doi.org/10.3389/fgene.2015.00148 |
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