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Microbe-host interplay in atopic dermatitis and psoriasis

Author

Listed:
  • Nanna Fyhrquist

    (Karolinska Institutet
    University of Helsinki)

  • Gareth Muirhead

    (King’s College London
    King’s College London)

  • Stefanie Prast-Nielsen

    (Karolinska Institutet)

  • Marine Jeanmougin

    (Institut Curie
    INSERM, U900
    Mines ParisTech
    INSERM, U932)

  • Peter Olah

    (University Hospital Duesseldorf
    University of Pécs)

  • Tiina Skoog

    (Karolinska Institutet)

  • Gerome Jules-Clement

    (Institut Curie
    INSERM, U900
    Mines ParisTech
    INSERM, U932)

  • Micha Feld

    (University Hospital Duesseldorf)

  • Mauricio Barrientos-Somarribas

    (Karolinska Institutet)

  • Hanna Sinkko

    (Karolinska Institutet
    University of Helsinki)

  • Ellen H. Bogaard

    (Radboud Institute for Molecular Life Sciences)

  • Patrick L.J.M. Zeeuwen

    (Radboud Institute for Molecular Life Sciences)

  • Gijs Rikken

    (Radboud Institute for Molecular Life Sciences)

  • Joost Schalkwijk

    (Radboud Institute for Molecular Life Sciences)

  • Hanna Niehues

    (Radboud Institute for Molecular Life Sciences)

  • Walter Däubener

    (Heinrich Heine University Duesseldorf)

  • Silvia Kathrin Eller

    (Heinrich Heine University Duesseldorf)

  • Helen Alexander

    (Kings College London)

  • Davide Pennino

    (King’s College London)

  • Sari Suomela

    (University of Helsinki and Helsinki University Hospital, Inflammation Centre)

  • Ioannis Tessas

    (University of Helsinki and Helsinki University Hospital, Inflammation Centre)

  • Emilia Lybeck

    (University of Helsinki and Helsinki University Hospital, Inflammation Centre)

  • Anna M. Baran

    (University Hospital Duesseldorf)

  • Hamid Darban

    (Karolinska Institutet)

  • Roopesh Singh Gangwar

    (The Hebrew University of Jerusalem)

  • Ulrich Gerstel

    (University Hospital Schleswig-Holstein)

  • Katharina Jahn

    (University Hospital Duesseldorf)

  • Piia Karisola

    (University of Helsinki)

  • Lee Yan

    (King’s College London)

  • Britta Hansmann

    (University Hospital Schleswig-Holstein)

  • Shintaro Katayama

    (Karolinska Institutet)

  • Stephan Meller

    (University Hospital Duesseldorf)

  • Max Bylesjö

    (Fios Genomics)

  • Philippe Hupé

    (Institut Curie
    INSERM, U900
    Mines ParisTech
    CNRS, UMR144)

  • Francesca Levi-Schaffer

    (The Hebrew University of Jerusalem)

  • Dario Greco

    (University of Tampere
    University of Tampere
    University of Helsinki)

  • Annamari Ranki

    (University of Helsinki and Helsinki University Hospital, Inflammation Centre)

  • Jens M. Schröder

    (University Hospital Schleswig-Holstein)

  • Jonathan Barker

    (Kings College London)

  • Juha Kere

    (Karolinska Institutet
    King’s College London)

  • Sophia Tsoka

    (King’s College London)

  • Antti Lauerma

    (University of Helsinki and Helsinki University Hospital, Inflammation Centre)

  • Vassili Soumelis

    (Institut Curie
    INSERM, U932)

  • Frank O. Nestle

    (King’s College London)

  • Bernhard Homey

    (University Hospital Duesseldorf)

  • Björn Andersson

    (Karolinska Institutet)

  • Harri Alenius

    (Karolinska Institutet
    University of Helsinki)

Abstract

Despite recent advances in understanding microbial diversity in skin homeostasis, the relevance of microbial dysbiosis in inflammatory disease is poorly understood. Here we perform a comparative analysis of skin microbial communities coupled to global patterns of cutaneous gene expression in patients with atopic dermatitis or psoriasis. The skin microbiota is analysed by 16S amplicon or whole genome sequencing and the skin transcriptome by microarrays, followed by integration of the data layers. We find that atopic dermatitis and psoriasis can be classified by distinct microbes, which differ from healthy volunteers microbiome composition. Atopic dermatitis is dominated by a single microbe (Staphylococcus aureus), and associated with a disease relevant host transcriptomic signature enriched for skin barrier function, tryptophan metabolism and immune activation. In contrast, psoriasis is characterized by co-occurring communities of microbes with weak associations with disease related gene expression. Our work provides a basis for biomarker discovery and targeted therapies in skin dysbiosis.

Suggested Citation

  • Nanna Fyhrquist & Gareth Muirhead & Stefanie Prast-Nielsen & Marine Jeanmougin & Peter Olah & Tiina Skoog & Gerome Jules-Clement & Micha Feld & Mauricio Barrientos-Somarribas & Hanna Sinkko & Ellen H., 2019. "Microbe-host interplay in atopic dermatitis and psoriasis," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12253-y
    DOI: 10.1038/s41467-019-12253-y
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    Cited by:

    1. Anissa Fries & Fanny Saidoune & François Kuonen & Isabelle Dupanloup & Nadine Fournier & Ana Cristina Guerra de Souza & Muzlifah Haniffa & Feiyang Ma & Johann E. Gudjonsson & Lennart Roesner & Yang Li, 2023. "Differentiation of IL-26+ TH17 intermediates into IL-17A producers via epithelial crosstalk in psoriasis," Nature Communications, Nature, vol. 14(1), pages 1-14, December.

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