Evidence map›Paper›PMID 23924613›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

A high-throughput screen for quorum-sensing inhibitors that target acyl-homoserine lactone synthases.

Quin H Christensen, Tyler L Grove, Squire J Booker, E Peter Greenberg

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. Research Progress on the Quorum Sensing System ofPathogens (Basel, Switzerland) · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Characterization of natural product inhibitors of quorum sensing inbioRxiv : the preprint server for biology · 2024
    Article
  7. Identification of a dCache-type chemoreceptor inFrontiers in microbiology · 2024
    Article
  8. Review
  9. Review
  10. Article
  11. Pseudomonas aeruginosa Quorum Sensing.Advances in experimental medicine and biology · 2022
    Article
  12. Article
  13. Article
  14. Bacterial quorum sensing quenching activity ofComputational and structural biotechnology journal · 2021
    Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. ACS chemical biology · 2019
    Article
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 2 institutions in 1 country.

Quin H ChristensenDepartment of Microbiology, University of Washington, Seattle, WA 98195, USA.
Tyler L Grove
Squire J Booker
E Peter Greenberg
Pennsylvania State University · USUniversity of Washington · US

Funding

Treatments for Nipah Virus InfectionU54AI057159 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI FINBERG, ROBERT WILLIAM · 2003 to 2013
$113.7M
Variation in Human Innate ImmunityU54AI057141 · NIAID · UNIVERSITY OF WASHINGTON · PI MILLER, SAMUEL I · 2003 to 2013
$102.3M
INTERDISCIPLINARY PROGRAM IN BACTERIAL PATHOGENESIST32AI055396 · NIAID · UNIVERSITY OF WASHINGTON · PI FANG, FERRIC C · 2003 to 2019
$2.8M
Functionalization of unactivated sp2-hybridized carbon atomsR01GM103268 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI BOLLINGER, JOSEPH M, BOOKER, SQUIRE J. · 2012 to 2015
$1.3M
Mechanisms of Radical-Dependent Biological MethylationR01GM101957 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI BOOKER, SQUIRE J. · 2012 to 2015
$1.0M
NIAID NIH HHS T32 AI055396NIAID NIH HHS T32AI055396NIAID NIH HHS U54 AI057141NIAID NIH HHS U54 AI057159NIGMS NIH HHS R01 GM101957NIGMS NIH HHS R01 GM103268
6 · The paper itself

Abstract

Many Proteobacteria use N-acyl-homoserine lactone (acyl-HSL) quorum sensing to control specific genes. Acyl-HSL synthesis requires unique enzymes that use S-adenosyl methionine as an acyl acceptor and amino acid donor. We developed and executed an enzyme-coupled high-throughput cell-free screen to discover acyl-HSL synthase inhibitors. The three strongest inhibitors were equally active against two different acyl-HSL synthases: Burkholderia mallei BmaI1 and Yersinia pestis YspI. Two of these inhibitors showed activity in whole cells. The most potent compound behaves as a noncompetitive inhibitor with a Ki of 0.7 µM and showed activity in a cell-based assay. Quorum-sensing signal synthesis inhibitors will be useful in attempts to understand acyl-HSL synthase catalysis and as a tool in studies of quorum-sensing control of gene expression. Because acyl-HSL quorum-sensing controls virulence of some bacterial pathogens, anti-quorum-sensing chemicals have been sought as potential therapeutic agents. Our screen and identification of acyl-HSL synthase inhibitors serve as a basis for efforts to target quorum-sensing signal synthesis as an antivirulence approach.

Indexed as

Acyl-ButyrolactonesEnzyme InhibitorsEscherichia coliFluorescenceGene Expression Regulation, BacterialHigh-Throughput Screening AssaysInhibitory Concentration 50KineticsLigasesMolecular StructureOxazinesProteobacteriaQuorum SensingAcyl-ButyrolactonesEnzyme InhibitorsLigasesOxazinesresorufinbacterial communicationcell–cell signalingenzyme inhibitors

Identifiers

PMID23924613
PMCPMC3752275
OpenAlexW2130540199

What OpenQuestion holds

Textmetadata
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.