Evidence map›Paper›PMID 26460240›Full record

ArticleChembiochem : a European journal of chemical biology2015

Potent and Selective Modulation of the RhlR Quorum Sensing Receptor by Using Non-native Ligands: An Emerging Target for Virulence Control in Pseudomonas aeruginosa.

Nora R Eibergen, Joseph D Moore, Margrith E Mattmann, Helen E Blackwell

Open access · greenAbstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Recent Advance in Small Molecules Targeting RhlR ofAntibiotics (Basel, Switzerland) · 2022
    Review
  13. Pseudomonas aeruginosa Quorum Sensing.Advances in experimental medicine and biology · 2022
    Article
  14. Curvularin Isolated FromFrontiers in microbiology · 2022
    Article
  15. Quorum Sensing Inhibitors to QuenchPharmaceuticals (Basel, Switzerland) · 2021
    Review
  16. Growing emergence of drug-resistantIranian journal of basic medical sciences · 2021
    Review
  17. Article
  18. Chemical Control of Quorum Sensing inACS infectious diseases · 2020
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Nora R EibergenDow Microbial Control, The Dow Chemical Company, 400 Arcola Road, Collegeville, PA, 19426, USA.
Joseph D MooreDow Microbial Control, The Dow Chemical Company, 400 Arcola Road, Collegeville, PA, 19426, USA.
Margrith E MattmannBiomatrica, Inc., 5627 Oberlin Drive, Suite 120, San Diego, CA, 92121, USA.
Helen E BlackwellDepartment of Chemistry, The University of Wisconsin-Madison, 1101 University Avenue, Madison, WI, 53706, USA. blackwell@chem.wisc.edu.
Dow Chemical (India) · INApplied BioMath (United States) · USUniversity of Wisconsin–Madison · US

Funding

BIOTECHNOLOGY TRAINING PROGRAMT32GM008349 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, BRIAN G · 1989 to 2019
$22.5M
Synthetic Ligands for Modulating Bacterial CommunicationR01GM109403 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BLACKWELL, HELEN E. · 2014 to 2017
$1.2M
Chemical Tools to Delineate the Pseudomonas aeruginosa Quorum Sensing CircuitF32GM100728 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI EIBERGEN, NORA R · 2012 to 2013
$101k
NIGMS NIH HHS 1F32 GM100728NIGMS NIH HHS F32 GM100728NIGMS NIH HHS GM109403NIGMS NIH HHS R01 GM109403NIGMS NIH HHS T32 GM008349NIGMS NIH HHS T32 GM08349
6 · The paper itself

Abstract

Pseudomonas aeruginosa uses N-acylated L-homoserine lactone signals and a triumvirate of LuxR-type receptor proteins--LasR, RhlR, and QscR--for quorum sensing (QS). Each of these receptors can contribute to QS activation or repression and, thereby, the control of myriad virulence phenotypes in this pathogen. LasR has traditionally been considered to be at the top of the QS receptor hierarchy in P. aeruginosa; however, recent reports suggest that RhlR plays a more prominent role in infection than originally predicted, in some circumstances superseding that of LasR. Herein, we report the characterization of a set of synthetic, small-molecule agonists and antagonists of RhlR. Using E. coli reporter strains, we demonstrated that many of these compounds can selectively activate or inhibit RhlR instead of LasR and QscR. Moreover, several molecules maintain their activities in P. aeruginosa at concentrations analogous to native RhlR signal levels. These compounds represent useful chemical probes to study the role of RhlR in the complex QS circuitry of P. aeruginosa, its direct (and indirect) effects on virulence, and its overall merit as a target for anti-infective therapy.

Indexed as

Ligands4-ButyrolactoneBacterial ProteinsEscherichia coliGenes, ReporterPhenotypeProtein BindingPseudomonas aeruginosaQuorum SensingSmall Molecule LibrariesVirulence4-ButyrolactoneBacterial Proteinshomoserine lactoneLigandsRhlR protein, Pseudomonas aeruginosaSmall Molecule Librarieslactone signalsLuxR-type receptorquorum sensingRhlRvirulence

Identifiers

PMID26460240
PMCPMC4648260
OpenAlexW2127128579

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.