Evidence map›Paper›PMID 22853441›Full record

ArticleACS chemical biology2012

Attenuation of quorum sensing in the pathogen Acinetobacter baumannii using non-native N-Acyl homoserine lactones.

Danielle M Stacy, Michael A Welsh, Philip N Rather, Helen E Blackwell

Abstract read
In one paragraph

Article in ACS chemical biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.4field-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

60 citing papers in PubMed, 108 citations in OpenAlex.

  1. MrtR ofProceedings of the National Academy of Sciences of the United States of America · 2026
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  13. International journal of molecular sciences · 2021
    Article
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  16. Pathogens (Basel, Switzerland) · 2021
    Review
  17. TheFrontiers in microbiology · 2021
    Article
  18. Review
  19. Review
  20. Quorum Sensing Inhibition or Quenching inFrontiers in microbiology · 2021
    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 2 institutions in 1 country.

Danielle M StacyDepartment of Chemistry, University of Madison-Wisconsin, Madison, Wisconsin 53706, United States.
Michael A Welsh
Philip N Rather
Helen E Blackwell
University of Wisconsin–Madison · USEmory University · US

Funding

Synthetic Ligands for Modulating Bacterial CommunicationR01AI063326 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI BLACKWELL, HELEN E. · 2006 to 2010
$1.1M
NIAID NIH HHS AI063326NIAID NIH HHS R01 AI063326
6 · The paper itself

Abstract

Many bacterial pathogens use quorum sensing (QS) to control virulence. As a result, the development of methods to intercept QS has attracted significant interest as a potential anti-infective therapy. Acinetobacter baumannii has emerged as a pan-drug-resistant pathogen and displays a remarkable ability to persist in hospital settings despite desiccation and antimicrobial treatment. Recent studies have shown that A. baumannii QS mutants have limited motility and fail to form mature biofilms; these phenotypes are linked to its ability to persist on biotic and abiotic surfaces and increase its pathogenicity. A. baumannii uses N-(3-hydroxydodecanoyl)-l-homoserine lactone (OH-dDHL) and its putative cognate receptor, AbaR, for QS. We sought to identify non-native ligands capable of blocking or promoting AbaR activity in A. baumannii for use as chemical probes to modulate QS phenotypes in this pathogen. We screened a focused library of synthetic, non-native N-acyl homoserine lactones (AHLs) to identify such compounds, and several highly potent antagonists and agonists were uncovered, with IC(50) and EC(50) values in the low micromolar range, respectively. The strongest AbaR antagonists largely contained aromatic acyl groups, whereas the AbaR agonists closely resembled OH-dDHL. Notably, the 10 most potent AbaR antagonists also strongly inhibited A. baumannii motility, and five antagonists reduced biofilm formation in A. baumannii by up to 40%. The discovery of these compounds is significant, as they represent, to our knowledge, the first non-native modulators of QS in A. baumannii to be reported and could find utility as new tools to study the role and timing of QS phenotypes in A. baumannii infections.

Indexed as

4-ButyrolactoneAcinetobacter baumanniiAcylationbeta-GalactosidaseBiofilmsDrug Resistance, Multiple, BacterialGenes, ReporterQuorum SensingRepressor ProteinsStructure-Activity Relationship4-Butyrolactonebeta-Galactosidasehomoserine lactoneRepressor Proteins

Identifiers

PMID22853441
PMCPMC3477293
OpenAlexW1990118809

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.