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Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation

Fructooligosaccharide (FOS), a prebiotic well known for its health-promoting properties, can improve the human gut ecosystem most likely through changes in its microbial composition. However, the detailed mechanism(s) of action of FOS in the modulation of the gut ecosystem remain(s) obscure. Traditi...

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Autores principales: Kato, Tamotsu, Fukuda, Shinji, Fujiwara, Akemi, Suda, Wataru, Hattori, Masahira, Kikuchi, Jun, Ohno, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195493/
https://www.ncbi.nlm.nih.gov/pubmed/24848698
http://dx.doi.org/10.1093/dnares/dsu013
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author Kato, Tamotsu
Fukuda, Shinji
Fujiwara, Akemi
Suda, Wataru
Hattori, Masahira
Kikuchi, Jun
Ohno, Hiroshi
author_facet Kato, Tamotsu
Fukuda, Shinji
Fujiwara, Akemi
Suda, Wataru
Hattori, Masahira
Kikuchi, Jun
Ohno, Hiroshi
author_sort Kato, Tamotsu
collection PubMed
description Fructooligosaccharide (FOS), a prebiotic well known for its health-promoting properties, can improve the human gut ecosystem most likely through changes in its microbial composition. However, the detailed mechanism(s) of action of FOS in the modulation of the gut ecosystem remain(s) obscure. Traditional methods of profiling microbes and metabolites could barely show any significant features due to the existence of large interindividual differences, but our novel microbe–metabolite correlation approach, combined with faecal immunoglobulin A (IgA) measurements, has revealed that the induction of mucosal IgA by FOS supplementation correlated with the presence of specific bacteria. Furthermore, the metabolic dynamics of butyrate, l-phenylalanine, l-lysine and tyramine were positively correlated with that of these bacteria and IgA production, whereas p-cresol was negatively correlated. Taken together, our focused intraindividual analysis with omics approaches is a powerful strategy for uncovering the gut molecular network and could provide a new vista for understanding the human gut ecosystem.
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spelling pubmed-41954932014-10-21 Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation Kato, Tamotsu Fukuda, Shinji Fujiwara, Akemi Suda, Wataru Hattori, Masahira Kikuchi, Jun Ohno, Hiroshi DNA Res Full Papers Fructooligosaccharide (FOS), a prebiotic well known for its health-promoting properties, can improve the human gut ecosystem most likely through changes in its microbial composition. However, the detailed mechanism(s) of action of FOS in the modulation of the gut ecosystem remain(s) obscure. Traditional methods of profiling microbes and metabolites could barely show any significant features due to the existence of large interindividual differences, but our novel microbe–metabolite correlation approach, combined with faecal immunoglobulin A (IgA) measurements, has revealed that the induction of mucosal IgA by FOS supplementation correlated with the presence of specific bacteria. Furthermore, the metabolic dynamics of butyrate, l-phenylalanine, l-lysine and tyramine were positively correlated with that of these bacteria and IgA production, whereas p-cresol was negatively correlated. Taken together, our focused intraindividual analysis with omics approaches is a powerful strategy for uncovering the gut molecular network and could provide a new vista for understanding the human gut ecosystem. Oxford University Press 2014-10 2014-05-19 /pmc/articles/PMC4195493/ /pubmed/24848698 http://dx.doi.org/10.1093/dnares/dsu013 Text en © The Author 2014. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Full Papers
Kato, Tamotsu
Fukuda, Shinji
Fujiwara, Akemi
Suda, Wataru
Hattori, Masahira
Kikuchi, Jun
Ohno, Hiroshi
Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation
title Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation
title_full Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation
title_fullStr Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation
title_full_unstemmed Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation
title_short Multiple Omics Uncovers Host–Gut Microbial Mutualism During Prebiotic Fructooligosaccharide Supplementation
title_sort multiple omics uncovers host–gut microbial mutualism during prebiotic fructooligosaccharide supplementation
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195493/
https://www.ncbi.nlm.nih.gov/pubmed/24848698
http://dx.doi.org/10.1093/dnares/dsu013
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