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Pectin-Derived Acidic Oligosaccharides Improve the Outcome of Pseudomonas aeruginosa Lung Infection in C57BL/6 Mice.

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  • Additional Information
    • Contributors:
      Lille Inflammation Research International Center - U 995 (LIRIC); Institut Pasteur de Lille; Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille); Nutricia Research; The study was funded by grants from the French Association "Vaincre la Mucoviscidose": grant number 2009/IC0916, 2010/IC1018) for purchasing mice and materials, and Nutricia Research for providing the experimental diets.; We thank the staff of the animal facility Dhure/IMPRT/IFR114.
    • Publication Information:
      HAL CCSD
      Public Library of Science
    • Publication Date:
      2015
    • Collection:
      Réseau International des Instituts Pasteur, Paris: HAL-RIIP
    • Abstract:
      International audience ; The administration of prebiotics as oligosaccharides (OS), by acting on intestinal microbiota, could modulate the immune and inflammatory response and represent a new strategy to improve the outcome of bacterial infection. The aim of this study was to determine whether pectin-derived acidic oligosaccharides (pAOS) could modulate the outcome of pulmonary P. aeruginosa (PA) infection in C57BL/6 mice, which develop a Th1 response to PA lung infection. Mice were randomized for 5 weeks to consume a control or a 5% pAOS diet and chronically infected by PA. Resistance to a second PA infection was also analyzed by reinfecting the surviving mice 2 weeks after the first infection. Compared with control mice, mice fed pAOS had reduced mortality (P<0.05). This improvement correlated with a better control of the inflammatory response with a lower neutrophil count on day 1 (P<0.05), a sustained neutrophil and macrophage recruitment on days 2 and 3 (P<0.01) a greater and sustained IL-10 release in lung (P<0.05) and a reduction of the Th1 response and M1 activation with a lower IFN-γ/IL-4 (P<0.01) and nos2/arg1 (P<0.05) ratios. These results coincided with a modulation of the intestinal microbiota as shown by an increased butyric acid concentration in feces (P<0.05). Moreover, pAOS decreased the bacterial load (P<0.01) in mice reinfected 2 weeks after the first infection, suggesting that pAOS could reduce pulmonary exacerbations. In conclusion, pAOS improved the outcome of PA infection in C57BL/6 mice by modulating the intestinal microbiota and the inflammatory and immune responses.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/26599638; hal-02178904; https://hal.univ-lille.fr/hal-02178904; https://hal.univ-lille.fr/hal-02178904/document; https://hal.univ-lille.fr/hal-02178904/file/PLoSOneHenry2015.pdf; PUBMED: 26599638; PUBMEDCENTRAL: PMC4658080
    • Accession Number:
      10.1371/journal.pone.0139686
    • Online Access:
      https://doi.org/10.1371/journal.pone.0139686
      https://hal.univ-lille.fr/hal-02178904
      https://hal.univ-lille.fr/hal-02178904/document
      https://hal.univ-lille.fr/hal-02178904/file/PLoSOneHenry2015.pdf
    • Rights:
      http://creativecommons.org/licenses/by/ ; info:eu-repo/semantics/OpenAccess
    • Accession Number:
      edsbas.84BC1AC3