Evidence map›Paper›PMID 22032541›Full record

ArticleBMC microbiology2011

Exploring the contribution of efflux on the resistance to fluoroquinolones in clinical isolates of Staphylococcus aureus.

Sofia Santos Costa, Celeste Falcão, Miguel Viveiros, Diana Machado, Marta Martins, José Melo-Cristino, Leonard Amaral, Isabel Couto

Erratum issuedAbstract read
In one paragraph

Article in BMC microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
–field-weighted citation impact
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

57 citing papers in PubMed.

  1. Article
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  3. Antimicrobials Resistance Profiling and Clonal Lineages ofJournal of arthropod-borne diseases · 2025
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  7. Enhanced Efficacy of Ciprofloxacin and Tobramycin againstAntibiotics (Basel, Switzerland) · 2024
    Article
  8. Article
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  10. Article
  11. Article
  12. Antibacterial Activity of the Essential Oil ofPlants (Basel, Switzerland) · 2023
    Article
  13. Review
  14. Inhibition ofAntibiotics (Basel, Switzerland) · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Occurrence and Variability of the Efflux Pump GeneInternational journal of molecular sciences · 2022
    Article
  19. Evaluation of Gene Expression ofArchives of Razi Institute · 2022
    Article
  20. Antibiotics (Basel, Switzerland) · 2022
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors.

Sofia Santos CostaGrupo de Micobactérias, Unidade de Microbiologia Médica, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa (IHMT, UNL), Rua da Junqueira 100, Lisbon, Portugal.
Celeste Falcão
Miguel Viveiros
Diana Machado
Marta Martins
José Melo-Cristino
Leonard Amaral
Isabel Couto

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntimicrobial resistance mediated by efflux systems is still poorly characterized in Staphylococcus aureus, despite the description of several efflux pumps (EPs) for this bacterium. In this work we used several methodologies to characterize the efflux activity of 52 S. aureus isolates resistant to ciprofloxacin collected in a hospital in Lisbon, Portugal, in order to understand the role played by these systems in the resistance to fluoroquinolones.

resultsAugmented efflux activity was detected in 12 out of 52 isolates and correlated with increased resistance to fluoroquinolones. Addition of efflux inhibitors did not result in the full reversion of the fluoroquinolone resistance phenotype, yet it implied a significant decrease in the resistance levels, regardless of the type(s) of mutation(s) found in the quinolone-resistance determining region of grlA and gyrA genes, which accounted for the remaining resistance that was not efflux-mediated. Expression analysis of the genes coding for the main efflux pumps revealed increased expression only in the presence of inducing agents. Moreover, it showed that not only different substrates can trigger expression of different EP genes, but also that the same substrate can promote a variable response, according to its concentration. We also found isolates belonging to the same clonal type that showed different responses towards drug exposure, thus evidencing that highly related clinical isolates may diverge in the efflux-mediated response to noxious agents. The data gathered by real-time fluorometric and RT-qPCR assays suggest that S. aureus clinical isolates may be primed to efflux antimicrobial compounds.

conclusionsThe results obtained in this work do not exclude the importance of mutations in resistance to fluoroquinolones in S. aureus, yet they underline the contribution of efflux systems for the emergence of high-level resistance. All together, the results presented in this study show the potential role played by efflux systems in the development of resistance to fluoroquinolones in clinical isolates of S. aureus.

Indexed as

Drug Resistance, BacterialAnti-Bacterial AgentsBacterial ProteinsDNA, BacterialDNA GyraseFluoroquinolonesHumansMembrane Transport ProteinsMicrobial Sensitivity TestsMutationStaphylococcal InfectionsStaphylococcus aureusAnti-Bacterial AgentsBacterial ProteinsDNA, BacterialDNA GyraseFluoroquinolonesMembrane Transport Proteins

Identifiers

PMID22032541
PMCPMC3226646

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LicenceCC BY
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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.