PUBLICATION

Host monitoring of quorum sensing during Pseudomonas aeruginosa infection

Authors
Moura-Alves, P., Puyskens, A., Stinn, A., Klemm, M., Guhlich-Bornhof, U., Dorhoi, A., Furkert, J., Kreuchwig, A., Protze, J., Lozza, L., Pei, G., Saikali, P., Perdomo, C., Mollenkopf, H.J., Hurwitz, R., Kirschhoefer, F., Brenner-Weiss, G., Weiner, J., Oschkinat, H., Kolbe, M., Krause, G., Kaufmann, S.H.E.
ID
ZDB-PUB-200403-256
Date
2019
Source
Science (New York, N.Y.)   366(6472): (Journal)
Registered Authors
Keywords
none
Datasets
GEO:GSE121101
MeSH Terms
  • A549 Cells
  • Animals
  • Mice, Knockout
  • Zebrafish
  • Pseudomonas aeruginosa/genetics
  • Pseudomonas aeruginosa/pathogenicity*
  • Pseudomonas Infections/microbiology*
  • Macrophages/microbiology
  • Receptors, Aryl Hydrocarbon/genetics
  • Receptors, Aryl Hydrocarbon/physiology*
  • Host-Pathogen Interactions*
  • Humans
  • Mice
  • Larva
  • Quorum Sensing/genetics
  • Quorum Sensing/physiology*
(all 16)
PubMed
31857448 Full text @ Science
Abstract
Pseudomonas aeruginosa rapidly adapts to altered conditions by quorum sensing (QS), a communication system that it uses to collectively modify its behavior through the production, release, and detection of signaling molecules. QS molecules can also be sensed by hosts, although the respective receptors and signaling pathways are poorly understood. We describe a pattern of regulation in the host by the aryl hydrocarbon receptor (AhR) that is critically dependent on qualitative and quantitative sensing of P. aeruginosa quorum. QS molecules bind to AhR and distinctly modulate its activity. This is mirrored upon infection with P. aeruginosa collected from diverse growth stages and with QS mutants. We propose that by spying on bacterial quorum, AhR acts as a major sensor of infection dynamics, capable of orchestrating host defense according to the status quo of infection.
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