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AhR sensing of bacterial pigments regulates antibacterial defence

Author

Listed:
  • Pedro Moura-Alves

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Kellen Faé

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Erica Houthuys

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Anca Dorhoi

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Annika Kreuchwig

    (Leibniz Institute for Molecular Pharmacology (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany)

  • Jens Furkert

    (Leibniz Institute for Molecular Pharmacology (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany)

  • Nicola Barison

    (Max Planck Institute for Infection Biology, Structural Systems Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Anne Diehl

    (Leibniz Institute for Molecular Pharmacology (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany)

  • Antje Munder

    (Clinical Research Group, Clinic for Pediatric Pneumology, Allergology and Neonatology, OE 6710, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany)

  • Patricia Constant

    (Institute of Pharmacology and Structural Biology (IPBS), CNRS and University of Toulouse (Toulouse III), 205 Route de Narbonne, 31077, Toulouse cedex 04, Toulouse, France)

  • Tatsiana Skrahina

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Ute Guhlich-Bornhof

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Marion Klemm

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Anne-Britta Koehler

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Silke Bandermann

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Christian Goosmann

    (Microscopy Core Facility, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Hans-Joachim Mollenkopf

    (Microarray Core Facility, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Robert Hurwitz

    (Protein Purification Core Facility, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Volker Brinkmann

    (Microscopy Core Facility, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Simon Fillatreau

    (German Rheumatism Research Centre Berlin (DRFZ), a Leibniz Institute, Charitéplatz 1, 10117 Berlin, Germany)

  • Mamadou Daffe

    (Institute of Pharmacology and Structural Biology (IPBS), CNRS and University of Toulouse (Toulouse III), 205 Route de Narbonne, 31077, Toulouse cedex 04, Toulouse, France)

  • Burkhard Tümmler

    (Clinical Research Group, Clinic for Pediatric Pneumology, Allergology and Neonatology, OE 6710, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany)

  • Michael Kolbe

    (Max Planck Institute for Infection Biology, Structural Systems Biology, Charitéplatz 1, 10117 Berlin, Germany)

  • Hartmut Oschkinat

    (Leibniz Institute for Molecular Pharmacology (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany)

  • Gerd Krause

    (Leibniz Institute for Molecular Pharmacology (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany)

  • Stefan H. E. Kaufmann

    (Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany)

Abstract

The aryl hydrocarbon receptor (AhR) is a highly conserved ligand-dependent transcription factor that senses environmental toxins and endogenous ligands, thereby inducing detoxifying enzymes and modulating immune cell differentiation and responses. We hypothesized that AhR evolved to sense not only environmental pollutants but also microbial insults. We characterized bacterial pigmented virulence factors, namely the phenazines from Pseudomonas aeruginosa and the naphthoquinone phthiocol from Mycobacterium tuberculosis, as ligands of AhR. Upon ligand binding, AhR activation leads to virulence factor degradation and regulated cytokine and chemokine production. The relevance of AhR to host defence is underlined by heightened susceptibility of AhR-deficient mice to both P. aeruginosa and M. tuberculosis. Thus, we demonstrate that AhR senses distinct bacterial virulence factors and controls antibacterial responses, supporting a previously unidentified role for AhR as an intracellular pattern recognition receptor, and identify bacterial pigments as a new class of pathogen-associated molecular patterns.

Suggested Citation

  • Pedro Moura-Alves & Kellen Faé & Erica Houthuys & Anca Dorhoi & Annika Kreuchwig & Jens Furkert & Nicola Barison & Anne Diehl & Antje Munder & Patricia Constant & Tatsiana Skrahina & Ute Guhlich-Bornh, 2014. "AhR sensing of bacterial pigments regulates antibacterial defence," Nature, Nature, vol. 512(7515), pages 387-392, August.
  • Handle: RePEc:nat:nature:v:512:y:2014:i:7515:d:10.1038_nature13684
    DOI: 10.1038/nature13684
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