Evidence map›Paper›PMID 16467145›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Quorum sensing and multidrug transporters in Escherichia coli.

Shirley Yang, Christopher R Lopez, E Lynn Zechiedrich

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 123 citations in OpenAlex.

  1. Observational
  2. Article
  3. Regulation of ofloxacin resistance inFrontiers in veterinary science · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Efflux, Signaling and Warfare in a Polymicrobial World.Antibiotics (Basel, Switzerland) · 2023
    Review
  10. Article
  11. Frontiers in microbiology · 2023
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Efflux pump inhibitors: new updates.Pharmacological reports : PR · 2021
    Review
  17. Review
  18. SdiA Improves the Acid Tolerance ofFrontiers in microbiology · 2020
    Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Shirley YangDepartment of Molecular Virology and Microbiology and Interdepartmental Program in Cell and Molecular Biology, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
Christopher R Lopez
E Lynn Zechiedrich
Baylor College of Medicine · US

Funding

COMBATTING QUINOLONE ANTIMICROBIAL RESISTANCER01AI054830 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI ZECHIEDRICH, LYNN · 2004 to 2012
$3.2M
RESEARCH TRAINING PROGRAM IN VIRAL ONCOLOGYT32CA009197 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MARRIOTT, SUSAN J · 1986 to 2003
$804k
NCI NIH HHS CA09197NCI NIH HHS T32 CA009197NIAID NIH HHS R01 AI054830
6 · The paper itself

Abstract

Previously, we found that the quorum sensing transcription factor SdiA up-regulates AcrAB. Others found that a 4-quinolone was a quorum-sensing signal in Pseudomonas aeruginosa. In Escherichia coli, there are at least three multidrug transporters (AcrAB/TolC, MdfA, and NorE) that exude fluoroquinolones. Here, we show that DeltaacrAB, tolC210, or DeltanorE mutants have the same growth rate as WT cells in exponential phase but grow to higher cell density in stationary phase. Overproduction of either pump caused cells to reach lower density. mdfA had no effect. Conditioned medium (CM) from cells overexpressing acrAB represses cell growth more than CM from WT cells. CM from pump mutant cells represses cell growth less than CM from WT cells. These results were not affected by the deletion of luxS, which synthesizes the quorum-sensing signal autoinducer 2 (AI-2). Expression of the rpoS gene encoding the stationary phase sigma factor is induced earlier in cells overexpressing acrAB and later in acrAB mutant cells. These results support a model in which a natural function of AcrAB/TolC and NorE is to export signals for cell-cell communication. Drugs exported by pumps may resemble communication molecules normally exuded.

Indexed as

ATP-Binding Cassette, Sub-Family C ProteinsBacterial Outer Membrane ProteinsBacterial ProteinsCarbon-Sulfur LyasesCulture Media, ConditionedDrug Resistance, Multiple, BacterialEscherichia coliEscherichia coli ProteinsGene DeletionGene Expression Regulation, BacterialGenes, BacterialLipoproteinsMembrane Transport ProteinsMutationSigma FactorTranscriptional ActivationAcrA protein, E coliAcrB protein, E coliATP-Binding Cassette, Sub-Family C ProteinsBacterial Outer Membrane ProteinsBacterial ProteinsCarbon-Sulfur LyasesCulture Media, ConditionedEscherichia coli ProteinsLipoproteinsLuxS protein, BacteriaMembrane Transport ProteinsSigma Factorsigma factor KatF protein, BacteriatolC protein, E coli

Identifiers

PMID16467145
PMCPMC1413681
OpenAlexW2070760655

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.