Cargando…
The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment
There is compelling evidence linking the commensal intestinal microbiota with host health and, in turn, antibiotic induced perturbations of microbiota composition with distinct pathologies. Despite the attractiveness of probiotic therapy as a tool to beneficially alter the intestinal microbiota, its...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418240/ https://www.ncbi.nlm.nih.gov/pubmed/28529928 http://dx.doi.org/10.3389/fcimb.2017.00167 |
_version_ | 1783234032707829760 |
---|---|
author | Ekmekciu, Ira von Klitzing, Eliane Fiebiger, Ulrike Neumann, Christian Bacher, Petra Scheffold, Alexander Bereswill, Stefan Heimesaat, Markus M. |
author_facet | Ekmekciu, Ira von Klitzing, Eliane Fiebiger, Ulrike Neumann, Christian Bacher, Petra Scheffold, Alexander Bereswill, Stefan Heimesaat, Markus M. |
author_sort | Ekmekciu, Ira |
collection | PubMed |
description | There is compelling evidence linking the commensal intestinal microbiota with host health and, in turn, antibiotic induced perturbations of microbiota composition with distinct pathologies. Despite the attractiveness of probiotic therapy as a tool to beneficially alter the intestinal microbiota, its immunological effects are still incompletely understood. The aim of the present study was to assess the efficacy of the probiotic formulation VSL#3 consisting of eight distinct bacterial species (including Streptococcus thermophilus, Bifidobacterium breve, B. longum, B. infantis, Lactobacillus acidophilus, L. plantarum, L. paracasei, and L. delbrueckii subsp. Bulgaricus) in reversing immunological effects of microbiota depletion as compared to reassociation with a complex murine microbiota. To address this, conventional mice were subjected to broad-spectrum antibiotic therapy for 8 weeks and perorally reassociated with either VSL#3 bacteria or a complex murine microbiota. VSL#3 recolonization resulted in restored CD4+ and CD8+ cell numbers in the small and large intestinal lamina propria as well as in B220+ cell numbers in the former, whereas probiotic intervention was not sufficient to reverse the antibiotic induced changes of respective cell populations in the spleen. However, VSL#3 application was as efficient as complex microbiota reassociation to attenuate the frequencies of regulatory T cells, activated dendritic cells and memory/effector T cells in the small intestine, colon, mesenteric lymph nodes, and spleen. Whereas broad-spectrum antibiotic treatment resulted in decreased production of cytokines such as IFN-γ, IL-17, IL-22, and IL-10 by CD4+ cells in respective immunological compartments, VSL#3 recolonization was sufficient to completely recover the expression of the anti-inflammatory cytokine IL-10 without affecting pro-inflammatory mediators. In summary, the probiotic compound VSL#3 has an extensive impact on mucosal, peripheral, and systemic innate as well as adaptive immunity, exerting beneficial anti-inflammatory effects in intestinal as well as systemic compartments. Hence, VSL#3 might be considered a therapeutic immunomodulatory tool following antibiotic therapy. |
format | Online Article Text |
id | pubmed-5418240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54182402017-05-19 The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment Ekmekciu, Ira von Klitzing, Eliane Fiebiger, Ulrike Neumann, Christian Bacher, Petra Scheffold, Alexander Bereswill, Stefan Heimesaat, Markus M. Front Cell Infect Microbiol Microbiology There is compelling evidence linking the commensal intestinal microbiota with host health and, in turn, antibiotic induced perturbations of microbiota composition with distinct pathologies. Despite the attractiveness of probiotic therapy as a tool to beneficially alter the intestinal microbiota, its immunological effects are still incompletely understood. The aim of the present study was to assess the efficacy of the probiotic formulation VSL#3 consisting of eight distinct bacterial species (including Streptococcus thermophilus, Bifidobacterium breve, B. longum, B. infantis, Lactobacillus acidophilus, L. plantarum, L. paracasei, and L. delbrueckii subsp. Bulgaricus) in reversing immunological effects of microbiota depletion as compared to reassociation with a complex murine microbiota. To address this, conventional mice were subjected to broad-spectrum antibiotic therapy for 8 weeks and perorally reassociated with either VSL#3 bacteria or a complex murine microbiota. VSL#3 recolonization resulted in restored CD4+ and CD8+ cell numbers in the small and large intestinal lamina propria as well as in B220+ cell numbers in the former, whereas probiotic intervention was not sufficient to reverse the antibiotic induced changes of respective cell populations in the spleen. However, VSL#3 application was as efficient as complex microbiota reassociation to attenuate the frequencies of regulatory T cells, activated dendritic cells and memory/effector T cells in the small intestine, colon, mesenteric lymph nodes, and spleen. Whereas broad-spectrum antibiotic treatment resulted in decreased production of cytokines such as IFN-γ, IL-17, IL-22, and IL-10 by CD4+ cells in respective immunological compartments, VSL#3 recolonization was sufficient to completely recover the expression of the anti-inflammatory cytokine IL-10 without affecting pro-inflammatory mediators. In summary, the probiotic compound VSL#3 has an extensive impact on mucosal, peripheral, and systemic innate as well as adaptive immunity, exerting beneficial anti-inflammatory effects in intestinal as well as systemic compartments. Hence, VSL#3 might be considered a therapeutic immunomodulatory tool following antibiotic therapy. Frontiers Media S.A. 2017-05-05 /pmc/articles/PMC5418240/ /pubmed/28529928 http://dx.doi.org/10.3389/fcimb.2017.00167 Text en Copyright © 2017 Ekmekciu, von Klitzing, Fiebiger, Neumann, Bacher, Scheffold, Bereswill and Heimesaat. 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 Ekmekciu, Ira von Klitzing, Eliane Fiebiger, Ulrike Neumann, Christian Bacher, Petra Scheffold, Alexander Bereswill, Stefan Heimesaat, Markus M. The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment |
title | The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment |
title_full | The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment |
title_fullStr | The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment |
title_full_unstemmed | The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment |
title_short | The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment |
title_sort | probiotic compound vsl#3 modulates mucosal, peripheral, and systemic immunity following murine broad-spectrum antibiotic treatment |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418240/ https://www.ncbi.nlm.nih.gov/pubmed/28529928 http://dx.doi.org/10.3389/fcimb.2017.00167 |
work_keys_str_mv | AT ekmekciuira theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT vonklitzingeliane theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT fiebigerulrike theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT neumannchristian theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT bacherpetra theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT scheffoldalexander theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT bereswillstefan theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT heimesaatmarkusm theprobioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT ekmekciuira probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT vonklitzingeliane probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT fiebigerulrike probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT neumannchristian probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT bacherpetra probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT scheffoldalexander probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT bereswillstefan probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment AT heimesaatmarkusm probioticcompoundvsl3modulatesmucosalperipheralandsystemicimmunityfollowingmurinebroadspectrumantibiotictreatment |