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AhR sensing of bacterial pigments regulates antibacterial defence
Author(s) -
Pedro MouraAlves,
Kellen C. Faé,
Erica Houthuys,
Anca Dorhoi,
Annika Kreuchwig,
Jens Furkert,
Nicola Barison,
Anne Diehl,
Antje Munder,
Patricia Constant,
Tatsiana Skrahina,
Ute Guhlich-Bornhof,
Marion Klemm,
Anne-Britta Koehler,
Silke Bandermann,
Christian Goosmann,
Hans-Joachim Mollenkopf,
Robert Hurwitz,
Volker Brinkmann,
Simon Fillatreau,
Mamadou Daffé,
Burkhard Tümmler,
Michael Kolbe,
Hartmut Oschkinat,
Gerd Krause,
Stefan H. E. Kaufmann
Publication year - 2014
Publication title -
nature
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 15.993
H-Index - 1226
eISSN - 1476-4687
pISSN - 0028-0836
DOI - 10.1038/nature13684
Subject(s) - aryl hydrocarbon receptor , virulence , pseudomonas aeruginosa , biology , virulence factor , microbiology and biotechnology , transcription factor , mycobacterium tuberculosis , pathogen , immune system , receptor , bacteria , genetics , gene , tuberculosis , medicine , pathology
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.

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