Evidence map›Paper›PMID 28510317›Full record

ArticleChembiochem : a European journal of chemical biology2017

Efflux Pumps Might Not Be the Major Drivers of QAC Resistance in Methicillin-Resistant Staphylococcus aureus.

Megan C Jennings, Megan E Forman, Stephanie M Duggan, Kevin P C Minbiole, William M Wuest

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-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

31 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. The mobilome landscape of biocide-resistance in Brazilian ESKAPE isolates.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Article
  6. Highly Effective Biocides againstACS infectious diseases · 2024
    Article
  7. Article
  8. Article
  9. Article
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  12. Review
  13. Article
  14. Article
  15. Merging antimicrobial and visible emission properties within 1,3,4-trisubstituted-1,2,3-triazolium salts.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2022
    Article
  16. Review
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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

5 authors at 2 institutions in 1 country.

Megan C JenningsDepartment of Chemistry, Temple University, 1901 N 13th Street, Philadelphia, PA, 19122, USA.
Megan E FormanDepartment of Chemistry, Villanova University, 800 E Lancaster Avenue, Villanova, PA, 19085, USA.
Stephanie M DugganDepartment of Chemistry, Villanova University, 800 E Lancaster Avenue, Villanova, PA, 19085, USA.
Kevin P C MinbioleDepartment of Chemistry, Villanova University, 800 E Lancaster Avenue, Villanova, PA, 19085, USA.
William M WuestDepartment of Chemistry, Temple University, 1901 N 13th Street, Philadelphia, PA, 19122, USA.
Villanova University · USTemple University · US

Funding

Natural Product-Inspired Approaches Toward The Development Of Antivirulence And Species-Specific InhibitorsR35GM119426 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI William M Wuest · 2016 to 2026
$4.8M
NIGMS NIH HHS R35 GM119426
6 · The paper itself

Abstract

Quaternary ammonium compounds (QACs) are commonly used antiseptics that are now known to be subject to bacterial resistance. The prevalence and mechanisms of such resistance, however, remain underexplored. We investigated a variety of QACs, including those with multicationic structures (multiQACs), and the resistance displayed by a variety of Staphylococcus aureus strains with and without genes encoding efflux pumps, the purported main driver of bacterial resistance in MRSA. Through minimum inhibitory concentration (MIC)-, kinetic-, and efflux-based assays, we found that neither the qacR/qacA system present in S. aureus nor another efflux pump system is the main reason for bacterial resistance to QACs. Our findings suggest that membrane composition could be the predominant driver that allows CA-MRSA to withstand the assault of conventional QAC antiseptics.

Indexed as

Anti-Infective Agents, LocalBacterial ProteinsBenzalkonium CompoundsCarbonyl Cyanide m-Chlorophenyl HydrazoneCell Membrane PermeabilityDrug Resistance, Multiple, BacterialMembrane Transport ModulatorsMembrane Transport ProteinsMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsRepressor ProteinsReserpineUncoupling AgentsAnti-Infective Agents, LocalBacterial ProteinsBenzalkonium CompoundsCarbonyl Cyanide m-Chlorophenyl HydrazoneMembrane Transport ModulatorsMembrane Transport ProteinsqacA protein, Staphylococcus aureusQacR protein, Staphylococcus aureusRepressor ProteinsReserpineUncoupling Agentsmethicillin-resistant Staphylococcus aureusqacquaternary ammonium compoundresistance

Identifiers

PMID28510317
PMCPMC5664203
OpenAlexW2614375732

What OpenQuestion holds

Textmetadata
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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.