Evidence map›Paper›PMID 30283991›Full record

ArticleCurrent microbiology2018

The Role of AcrAB-TolC Efflux Pumps on Quinolone Resistance of E. coli ST131.

N Atac, O Kurt-Azap, I Dolapci, A Yesilkaya, O Ergonul, M Gonen, F Can

Abstract read
PubMed Publisher
In one paragraph

Article in Current microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. No two are alike: on the role ofAntimicrobial agents and chemotherapy · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Comparison of Phenotype and Genotype Virulence and Antimicrobial Factors ofInternational journal of molecular sciences · 2023
    Article
  11. Infection and drug resistance · 2023
    Article
  12. Article
  13. Antimicrobial ResistantFoods (Basel, Switzerland) · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

7 authors at 3 institutions in 1 country.

N AtacDepartment of Medical Microbiology, Koc University School of Medicine, Istanbul, Turkey. natac@ku.edu.tr.
O Kurt-AzapDepartment of Infectious Diseases and Clinical Microbiology, Baskent University School of Medicine, Ankara, Turkey.
I DolapciDepartment of Medical Microbiology, Ankara University School of Medicine, Ankara, Turkey.
A YesilkayaDepartment of Infectious Diseases and Clinical Microbiology, Baskent University School of Medicine, Ankara, Turkey.
O ErgonulDepartment of Infectious Diseases and Clinical Microbiology, Koc University School of Medicine, Istanbul, Turkey.
M GonenIndustrial Engineering, Koc University College of Engineering, Istanbul, Turkey.
F CanDepartment of Medical Microbiology, Koc University School of Medicine, Istanbul, Turkey.
Koç University · TRBaşkent University · TRAnkara University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Escherichia coli ST131 is a cause for global concern because of its high multidrug resistance and several virulence factors. In this study, the contribution of acrAB-TolC efflux system of E. coli ST131 to fluoroquinolone resistance was evaluated. A total of nonrepetitive 111 ciprofloxacin-resistant E. coli isolates were included in the study. Multilocus sequence typing was used for genotyping. Expressions of acrA, acrB, and TolC efflux pump genes were measured by RT-PCR. Mutations in marA, gyrA, parC, and aac(6')-lb-cr positivity were studied by Sanger sequencing. Sixty-four (57.7%) of the isolates were classified as ST131, and 52 (81.3%) of the ST131 isolates belonged to H30-Rx subclone. In ST131, CTX-M 15 positivity (73%) and aac(6')-lb-cr carriage (75%) were significantly higher than those in non-ST131 (12.8% and 51%, respectively) (P < 0.05). The ampicillin-sulbactam (83%) resistance was higher, and gentamicin resistance (20%) was lower in ST131 than that in non-ST131 (64% and 55%, respectively) (P = 0.001 and P = 0.0002). Numbers of the isolates with MDR or XDR profiles did not differ in both groups. Multiple in-dels (up to 16) were recorded in all quinolone-resistant isolates. However, marA gene was more overexpressed in ST131 compared to that in non-ST131 (median 5.98 vs. 3.99; P = 0.0007). Belonging to H30-Rx subclone, isolation site, ciprofloxacin MIC values did not correlate with efflux pump expressions. In conclusion, the marA regulatory gene of AcrAB-TolC efflux pump system has a significant impact on quinolone resistance and progression to MDR profile in ST131 clone. Efflux pump inhibitors might be alternative drugs for the treatment of infections caused by E. coli ST131 if used synergistically in combination with antibiotics.

Indexed as

Anti-Bacterial AgentsCarrier ProteinsDrug Resistance, Multiple, BacterialEscherichia coliEscherichia coli InfectionsEscherichia coli ProteinsHumansMicrobial Sensitivity TestsMultilocus Sequence TypingQuinolonesVirulence FactorsAcrAB-TolC protein, E coliAnti-Bacterial AgentsCarrier ProteinsEscherichia coli ProteinsQuinolonesVirulence Factors

Identifiers

PMID30283991
OpenAlexW2894632725

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.