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Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties
In this study we explored the immunomodulatory properties of highly purified free galactan, the soluble exopolysaccharide secreted by Mycoplasma mycoides subsp. mycoides (Mmm). Galactan was shown to bind to TLR2 but not TLR4 using HEK293 reporter cells and to induce the production of the anti-inflam...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618858/ https://www.ncbi.nlm.nih.gov/pubmed/26490663 http://dx.doi.org/10.1186/s13567-015-0252-6 |
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author | Totté, Philippe Puech, Carinne Rodrigues, Valérie Bertin, Clothilde Manso-Silvan, Lucia Thiaucourt, François |
author_facet | Totté, Philippe Puech, Carinne Rodrigues, Valérie Bertin, Clothilde Manso-Silvan, Lucia Thiaucourt, François |
author_sort | Totté, Philippe |
collection | PubMed |
description | In this study we explored the immunomodulatory properties of highly purified free galactan, the soluble exopolysaccharide secreted by Mycoplasma mycoides subsp. mycoides (Mmm). Galactan was shown to bind to TLR2 but not TLR4 using HEK293 reporter cells and to induce the production of the anti-inflammatory cytokine IL-10 in bovine macrophages, whereas low IL-12p40 and no TNF-α, both pro-inflammatory cytokines, were induced in these cells. In addition, pre-treatment of macrophages with galactan substantially reduced lipopolysaccharide (LPS)-induced production of pro-inflammatory cytokines TNF- and IL-12p40 while increasing LPS-induced secretion of immunosuppressive IL-10. Also, galactan did not activate naïve lymphocytes and induced only low production of the Th1 cytokine IFN-γ in Mmm-experienced lymphocytes. Finally, galactan triggered weak recall proliferation of CD4+ T lymphocytes from contagious bovine pleuropneumonia-infected animals despite having a positive effect on the expression of co-stimulatory molecules on macrophages. All together, these results suggest that galactan possesses anti-inflammatory properties and potentially provides Mmm with a mechanism to evade host innate and adaptive cell-mediated immune responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0252-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4618858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46188582015-10-25 Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties Totté, Philippe Puech, Carinne Rodrigues, Valérie Bertin, Clothilde Manso-Silvan, Lucia Thiaucourt, François Vet Res Research Article In this study we explored the immunomodulatory properties of highly purified free galactan, the soluble exopolysaccharide secreted by Mycoplasma mycoides subsp. mycoides (Mmm). Galactan was shown to bind to TLR2 but not TLR4 using HEK293 reporter cells and to induce the production of the anti-inflammatory cytokine IL-10 in bovine macrophages, whereas low IL-12p40 and no TNF-α, both pro-inflammatory cytokines, were induced in these cells. In addition, pre-treatment of macrophages with galactan substantially reduced lipopolysaccharide (LPS)-induced production of pro-inflammatory cytokines TNF- and IL-12p40 while increasing LPS-induced secretion of immunosuppressive IL-10. Also, galactan did not activate naïve lymphocytes and induced only low production of the Th1 cytokine IFN-γ in Mmm-experienced lymphocytes. Finally, galactan triggered weak recall proliferation of CD4+ T lymphocytes from contagious bovine pleuropneumonia-infected animals despite having a positive effect on the expression of co-stimulatory molecules on macrophages. All together, these results suggest that galactan possesses anti-inflammatory properties and potentially provides Mmm with a mechanism to evade host innate and adaptive cell-mediated immune responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0252-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-21 2015 /pmc/articles/PMC4618858/ /pubmed/26490663 http://dx.doi.org/10.1186/s13567-015-0252-6 Text en © Totté et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Totté, Philippe Puech, Carinne Rodrigues, Valérie Bertin, Clothilde Manso-Silvan, Lucia Thiaucourt, François Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
title | Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
title_full | Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
title_fullStr | Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
title_full_unstemmed | Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
title_short | Free exopolysaccharide from Mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
title_sort | free exopolysaccharide from mycoplasma mycoides subsp. mycoides possesses anti-inflammatory properties |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618858/ https://www.ncbi.nlm.nih.gov/pubmed/26490663 http://dx.doi.org/10.1186/s13567-015-0252-6 |
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