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Crucial Role of Microbiota in Experimental Psoriasis Revealed by a Gnotobiotic Mouse Model

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    SYSNO ASEP0523660
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleCrucial Role of Microbiota in Experimental Psoriasis Revealed by a Gnotobiotic Mouse Model
    Author(s) Stehlíková, Z. (CZ)
    Kostovčíková, Klára (UMG-J)
    Kverka, Miloslav (UEM-P)
    Rossmann, P. (CZ)
    Dvorak, J. (CZ)
    Novosádová, I. (CZ)
    Kostovčík, M. (CZ)
    Coufal, Š. (CZ)
    Šrůtková, D. (CZ)
    Procházková, P. (CZ)
    Hudcovic, T. (CZ)
    Kozáková, H. (CZ)
    Stěpánková, R. (CZ)
    Rob, F. (CZ)
    Jůzlová, K. (CZ)
    Hercogová, J. (CZ)
    Tlaskalová-Hogenová, H. (CZ)
    Zákostelská, Z. (CZ)
    Number of authors18
    Article number236
    Source TitleFrontiers in Microbiology. - : Frontiers Research Foundation - ISSN 1664-302X
    Roč. 10, Feb 21 (2019)
    Number of pages11 s.
    Publication formOnline - E
    Languageeng - English
    CountryCH - Switzerland
    Keywordspsoriasis ; antibiotics ; microbiota ; germ-free ; animal model ; imiquimod ; intestine ; skin
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryMicrobiology
    Method of publishingOpen access
    Institutional supportUMG-J - RVO:68378050
    UT WOS000459260100001
    DOI10.3389/fmicb.2019.00236
    AnnotationPsoriatic patients have altered microbiota, both in the intestine and on the skin. It is not clear, however, whether this is a cause or consequence of the disease. In this study, using an experimental mouse model of psoriasis induced by imiquimod (IMO), we show that oral treatment with a broad spectrum of antibiotics (MIX) or metronidazole (MET) alone mitigates the severity of skin inflammation through downregulation of Th17 immune response in conventional mice. Since some antibiotics, including MET, can influence immune system reactivity, we also evaluated the effect of MIX in the same model under germ-free (GF) conditions. GF mice treated with MET did not show milder signs of imiquimod-induced skin inflammation (IISI) which supports the conclusion that the therapeutic effect is mediated by changes in microbiota composition. Moreover, compared to controls, mice treated with MIX had a significantly higher abundance of the genus Lactobacillus in the intestine and on the skin. Mice treated with MET had a significantly higher abundance of the genera Bifidobacterium and Enterococcus both on the skin and in the intestine and of Parabacteroides distasonis in the intestine. Additionally, GF mice and mice monocolonized with either Lactobacillus plantarum or segmented filamentous bacteria (SFB) were more resistant to IISI than conventional mice. Interestingly, compared to GF mice, IMQ induced a higher degree of systemic Th17 activation in mice monocolonized with SFB but not with L. plantarum. The present findings provide evidence that intestinal and skin microbiota directly regulates IISI and emphasizes the importance of microbiota in the pathogenesis of psoriasis.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2020
    Electronic addresshttps://www.frontiersin.org/articles/10.3389/fmicb.2019.00236/full
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