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Bifidobacteria and Their Molecular Communication with the Immune System

Bifidobacterium represents a genus within the phylum Actinobacteria which is one of the major phyla in the healthy intestinal tract of humans. Bifidobacterium is one of the most abundant genera in adults, but its predominance is even more pronounced in infants, especially during lactation, when they...

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Autores principales: Ruiz, Lorena, Delgado, Susana, Ruas-Madiedo, Patricia, Sánchez, Borja, Margolles, Abelardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722804/
https://www.ncbi.nlm.nih.gov/pubmed/29255450
http://dx.doi.org/10.3389/fmicb.2017.02345
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author Ruiz, Lorena
Delgado, Susana
Ruas-Madiedo, Patricia
Sánchez, Borja
Margolles, Abelardo
author_facet Ruiz, Lorena
Delgado, Susana
Ruas-Madiedo, Patricia
Sánchez, Borja
Margolles, Abelardo
author_sort Ruiz, Lorena
collection PubMed
description Bifidobacterium represents a genus within the phylum Actinobacteria which is one of the major phyla in the healthy intestinal tract of humans. Bifidobacterium is one of the most abundant genera in adults, but its predominance is even more pronounced in infants, especially during lactation, when they can constitute the majority of the total bacterial population. They are one of the pioneering colonizers of the early gut microbiota, and they are known to play important roles in the metabolism of dietary components, otherwise indigestible in the upper parts of the intestine, and in the maturation of the immune system. Bifidobacteria have been shown to interact with human immune cells and to modulate specific pathways, involving innate and adaptive immune processes. In this mini-review, we provide an overview of the current knowledge on the immunomodulatory properties of bifidobacteria and the mechanisms and molecular players underlying these processes, focusing on the corresponding implications for human health. We deal with in vitro models suitable for studying strain-specific immunomodulatory activities. These include peripheral blood mononuclear cells and T cell-mediated immune responses, both effector and regulatory cell responses, as well as the modulation of the phenotype of dendritic cells, among others. Furthermore, preclinical studies, mainly germ-free, gnotobiotic, and conventional murine models, and human clinical trials, are also discussed. Finally, we highlight evidence supporting the immunomodulatory effects of bifidobacterial molecules (proteins and peptides, exopolysaccharides, metabolites, and DNA), as well as the role of bifidobacterial metabolism in maintaining immune homeostasis through cross-feeding mechanisms.
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spelling pubmed-57228042017-12-18 Bifidobacteria and Their Molecular Communication with the Immune System Ruiz, Lorena Delgado, Susana Ruas-Madiedo, Patricia Sánchez, Borja Margolles, Abelardo Front Microbiol Microbiology Bifidobacterium represents a genus within the phylum Actinobacteria which is one of the major phyla in the healthy intestinal tract of humans. Bifidobacterium is one of the most abundant genera in adults, but its predominance is even more pronounced in infants, especially during lactation, when they can constitute the majority of the total bacterial population. They are one of the pioneering colonizers of the early gut microbiota, and they are known to play important roles in the metabolism of dietary components, otherwise indigestible in the upper parts of the intestine, and in the maturation of the immune system. Bifidobacteria have been shown to interact with human immune cells and to modulate specific pathways, involving innate and adaptive immune processes. In this mini-review, we provide an overview of the current knowledge on the immunomodulatory properties of bifidobacteria and the mechanisms and molecular players underlying these processes, focusing on the corresponding implications for human health. We deal with in vitro models suitable for studying strain-specific immunomodulatory activities. These include peripheral blood mononuclear cells and T cell-mediated immune responses, both effector and regulatory cell responses, as well as the modulation of the phenotype of dendritic cells, among others. Furthermore, preclinical studies, mainly germ-free, gnotobiotic, and conventional murine models, and human clinical trials, are also discussed. Finally, we highlight evidence supporting the immunomodulatory effects of bifidobacterial molecules (proteins and peptides, exopolysaccharides, metabolites, and DNA), as well as the role of bifidobacterial metabolism in maintaining immune homeostasis through cross-feeding mechanisms. Frontiers Media S.A. 2017-12-04 /pmc/articles/PMC5722804/ /pubmed/29255450 http://dx.doi.org/10.3389/fmicb.2017.02345 Text en Copyright © 2017 Ruiz, Delgado, Ruas-Madiedo, Sánchez and Margolles. 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 Microbiology
Ruiz, Lorena
Delgado, Susana
Ruas-Madiedo, Patricia
Sánchez, Borja
Margolles, Abelardo
Bifidobacteria and Their Molecular Communication with the Immune System
title Bifidobacteria and Their Molecular Communication with the Immune System
title_full Bifidobacteria and Their Molecular Communication with the Immune System
title_fullStr Bifidobacteria and Their Molecular Communication with the Immune System
title_full_unstemmed Bifidobacteria and Their Molecular Communication with the Immune System
title_short Bifidobacteria and Their Molecular Communication with the Immune System
title_sort bifidobacteria and their molecular communication with the immune system
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722804/
https://www.ncbi.nlm.nih.gov/pubmed/29255450
http://dx.doi.org/10.3389/fmicb.2017.02345
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