Evidence map›Paper›PMID 39488602›Full record

ArticleScientific reports2024

Analysis of molecular mechanisms of delafloxacin resistance in Escherichia coli.

András Kubicskó, Katalin Kamotsay, Dóra Szabó, Béla Kocsis

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Delafloxacin: what does a new fluoroquinolone offer?Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2026
    Review
  2. Article
  3. VariableAntibiotics (Basel, Switzerland) · 2025
    Article
  4. Article
  5. Article
  6. Review
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.

András KubicskóInstitute of Medical Microbiology, Semmelweis University, 1089, Budapest, Hungary.
Katalin KamotsayCentral Microbiology Laboratory, National Institute of Hematology and Infectious Disease, Central Hospital of Southern-Pest, 1097, Budapest, Hungary.
Dóra SzabóInstitute of Medical Microbiology, Semmelweis University, 1089, Budapest, Hungary.
Béla KocsisInstitute of Medical Microbiology, Semmelweis University, 1089, Budapest, Hungary. kocsis.bela@med.semmelweis-univ.hu.

Funding

European Union's Horizon 2020 research and innovation program 952491-AmReSuHungarian Academy of Sciences János Bolyai Research Scholarship (BO/00286/22/5)HUN-REN-SU Human Microbiota Research Group No "0272".
6 · The paper itself

Abstract

In this study delafloxacin resistance mechanisms in Escherichia coli strains were analyzed. Delafloxacin is a new fluoroquinolone, that is approved for clinical application however, resistance against this agent is scarcely reported. In our study 37 E. coli strains were included and antimicrobial susceptibility testing was performed for ciprofloxacin, delafloxacin, levofloxacin, moxifloxacin, ceftazidime, cefotaxime, imipenem. Six delafloxacin resistant E. coli strains were selected for whole-genome sequencing and all of them exhibited resistance to other fluoroquinonlones and showed an extended-spectrum beta-lactamase phenotype. The six delafloxacin resistant E. coli strains belonged to different sequence types (STs) namely, ST131 (2 strains), ST57 (2 strains), ST162 and ST15840. Each delafloxacin resistant strain possessed multiple mutations in quinolone resistance-determining regions (QRDRs). Notably, three mutations in gyrA Ser83Leu, Asp87Asn and parC Ser80Ile were in strains of ST162, ST57 and ST15840. However, the two strains of ST131 carried five combined mutations namely, gyrA Ser83Leu, Asp87Asn, parC Ser80Ile, Glu84Val, parE Ile549Leu. Association of delafloxacin resistance and production of CTX-M-15 in ST131, CMY-2 in ST162 and ST15840 was detected. In this study a new ST, ST15840 of clonal complex 69 was identified. Our results demonstrate, that at least three mutations in QRDRs are required for delafloxacin resistance in E. coli.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialEscherichia coliFluoroquinolonesMicrobial Sensitivity Testsbeta-LactamasesDNA GyraseDNA Topoisomerase IVEscherichia coli InfectionsHumansMutationWhole Genome SequencingAnti-Bacterial Agentsbeta-LactamasesdelafloxacinDNA GyraseDNA Topoisomerase IVFluoroquinolonesAmpCDelafloxacinESBLFluoroquinolone resistanceHigh-risk cloneWGS

Identifiers

PMID39488602
PMCPMC11531523

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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.