Evidence map›Paper›PMID 31752702›Full record

ArticleBMC infectious diseases2019

Impact of co-existence of PMQR genes and QRDR mutations on fluoroquinolones resistance in Enterobacteriaceae strains isolated from community and hospital acquired UTIs.

Dalia Nabil Kotb, Wafaa Khairy Mahdy, Mahmoud Shokry Mahmoud, Rasha M M Khairy

Abstract read
In one paragraph

Article in BMC infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

39 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Global prevalence of fluoroquinolone resistance inFrontiers in cellular and infection microbiology · 2026
    Pooled it
  2. Article
  3. CTX-M variants on the move: Tracking resistance inOne health (Amsterdam, Netherlands) · 2026
    Article
  4. Review
  5. Detection and Characterization of ThermotolerantAntibiotics (Basel, Switzerland) · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Fluoroquinolone Resistance inMicroorganisms · 2024
    Review
  17. Article
  18. Article
  19. The Abundance of Plasmid-Mediated Quinolone Resistance Genes inThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2024
    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

4 authors.

Dalia Nabil KotbDepartment of Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, 61511, Egypt.
Wafaa Khairy MahdyDepartment of Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, 61511, Egypt.
Mahmoud Shokry MahmoudDepartment of Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, 61511, Egypt.
Rasha M M KhairyDepartment of Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, 61511, Egypt. rashakhiry1@gmail.com.ORCID http://orcid.org/0000-0003-4481-8608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFluoroquinolones are commonly recommended as treatment for urinary tract infections (UTIs). The development of resistance to these agents, particularly in gram-negative microorganisms complicates treatment of infections caused by these organisms. This study aimed to investigate antimicrobial resistance of different Enterobacteriaceae species isolated from hospital- acquired and community-acquired UTIs against fluoroquinolones and correlate its levels with the existing genetic mechanisms of resistance.

methodsA total of 440 Enterobacteriaceae isolates recovered from UTIs were tested for antimicrobial susceptibility. Plasmid-mediated quinolone resistance (PMQR) genes and mutations in the quinolone resistance-determining regions (QRDRs) of gyrA and parC genes were examined in quinolone-resistant strains.

resultsAbout (32.5%) of isolates were resistant to quinolones and (20.5%) were resistant to fluoroquinolones. All isolates with high and intermediate resistance phenotypes harbored one or more PMQR genes. QnrB was the most frequent gene (62.9%) of resistant isolates. Co-carriage of 2 PMQR genes was detected in isolates (46.9%) with high resistance to ciprofloxacin (CIP) (MICs > 128 μg/mL), while co-carriage of 3 PMQR genes was detected in (6.3%) of resistant isolates (MICs > 512 μg/mL). Carriage of one gene only was detected in intermediate resistance isolates (MICs of CIP = 1.5-2 μg/mL). Neither qnrA nor qnrC genes were detected. The mutation at code 83 of gyrA was the most frequent followed by Ser80-Ile in parC gene, while Asp-87 Asn mutation of gyrA gene was the least, where it was detected only in high resistant E. coli isolates (MIC ≥128 μg/mL). A double mutation in gyrA (Lys154Arg and Ser171Ala) was observed in high FQs resistant isolates (MIC of CIP < 128 μg/mL).

conclusionFQs resistance is caused by interact between PMQR genes and mutations in both gyrA and parC genes while a mutation in one gene only can explain quinolone resistance. Accumulation of PMQR genes and QRDR mutations confers high resistance to FQs.

Indexed as

Drug Resistance, BacterialAdultAnti-Bacterial AgentsBacterial ProteinsCiprofloxacinCross InfectionEnterobacteriaceaeEnterobacteriaceae InfectionsFemaleFluoroquinolonesHumansMaleMicrobial Sensitivity TestsMiddle AgedMutationPlasmidsAnti-Bacterial AgentsBacterial ProteinsCiprofloxacinFluoroquinolonesQuinolonesEnterobacteriaceaeFluoroquinolonesPlasmid-mediated quinolone resistanceQuinolone resistance-determining regions (QRDRs)

Identifiers

PMID31752702
PMCPMC6868749

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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.