PqsE Is Essential for RhlR-Dependent Quorum Sensing Regulation in Pseudomonas aeruginosa

Marie-Christine Groleau1, Thays de Oliveira Pereira1, Valérie Dekimpe1

  • 1Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique (INRS), Laval, Quebec, Canada.

Msystems
|May 28, 2020
PubMed

Insights

Pseudomonas aeruginosa quorum sensing (QS) regulation is re-evaluated, identifying RhlR as the primary regulator and PqsE as crucial for activating RhlR-dependent QS, especially when LasR is absent.

Area of Science:

  • Microbiology
  • Bacterial Pathogenesis
  • Molecular Biology

Background:

  • Pseudomonas aeruginosa is a critical healthcare-associated pathogen causing diverse infections.
  • Its virulence and survival are regulated by three interconnected quorum sensing (QS) systems: las, rhl, and pqs.
  • The las system is traditionally viewed as the master regulator, controlling rhl and pqs systems.

Purpose of the Study:

  • To clarify the hierarchical regulation among Pseudomonas aeruginosa QS systems.
  • To determine the primary regulator of C4-HSL production and RhlR-dependent gene expression.
  • To elucidate the role of PqsE in QS activation.

Main Methods:

  • Utilized liquid chromatography-mass spectrometry for autoinducer quantification.
  • Employed gene expression reporters to monitor QS system activity.
  • Investigated RhlR target gene expression under varying conditions.

Main Results:

  • Confirmed LasR as the principal regulator of C4-HSL production, not RhlR.
  • Demonstrated that RhlR regulates rhlI and C4-HSL production mainly in the absence of LasR.
  • Showed that PqsE is essential for activating RhlR-dependent QS, particularly when LasR is non-functional.

Conclusions:

  • This study repositions RhlR as the key QS regulator in P. aeruginosa.
  • Highlights PqsE as a critical effector for full QS activation, especially in LasR-deficient scenarios.
  • Suggests PqsE as a potential therapeutic target to control P. aeruginosa virulence, particularly in chronic infections where LasR mutants are common.

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