Evidence map›Paper›PMID 41635259›Full record

ArticleThe Journal of infectious diseases2026

Epidemiological and Molecular Surveillance of Multiresistant Citrobacter freundii Complex in a Tertiary Care Hospital: A Retrospective Cohort Study.

Pérince Fonton, Roberto Sierra, Romain Martischang, Aude Nguyen, Abdessalam Cherkaoui, Diego O Andrey, Stephan Harbarth

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. TheInternational journal of molecular sciences · 2026
    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

7 authors.

Pérince FontonInfection Control Program, Geneva University Hospitals and Faculty of Medicine, WHO Collaborating Center, Geneva, Switzerland.
Roberto SierraDepartment of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Romain MartischangInfectious Diseases Division, Department of Medicine, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.ORCID 0000-0001-5071-0893
Aude NguyenInfectious Diseases Division, Department of Medicine, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
Abdessalam CherkaouiDivision of Laboratory Medicine, Diagnostics Department, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
Diego O AndreyDepartment of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID 0000-0003-3247-9274
Stephan HarbarthInfection Control Program, Geneva University Hospitals and Faculty of Medicine, WHO Collaborating Center, Geneva, Switzerland.ORCID 0000-0002-3551-1025

Funding

Federal CommissionGeneva University HospitalsJoint Programming Initiative on Antimicrobial ResistanceResearch and Development ProgramSchweizerischer National Fonds 40JP40_218865Swiss Government Excellence 2022.0465
6 · The paper itself

Abstract

backgroundCitrobacter freundii is an emerging nosocomial pathogen, yet its transmission dynamics remain poorly characterized.

methodsWe conducted a retrospective genomic and epidemiological study to investigate the transmission chains of extended-spectrum beta-lactamase (ESBL) and carbapenemase-producing C. freundii collected at Geneva University Hospitals during a 6-year period (2017-2022). Whole-genome sequencing (WGS) using Nanopore long-read sequencing, MLST and plasmid typing, and resistome profiling were performed. Transmission events were defined based on genetic relatedness, plasmid similarity and patient trajectories.

resultsA total of 103 cases of ESBL and carbapenemase-producing C. freundii were identified, of which 79% were hospital-acquired, 72% were isolated from rectal swabs, and bacteremia occurred in 6 patients. Among 90 isolates available for WGS, 73% were confirmed as C. freundii, whereas the remaining belonged to other Citrobacter species. A high genetic diversity was observed among C. freundii sensu stricto, with 29 distinct sequence types, including predominant ST114, ST98, and ST22. We identified 10 clusters involving multiple Citrobacter species among 35 patients, with a median cluster duration of 103 weeks (IQR, 65-138). Transmission chain analysis revealed that 37% of patients were involved in putative clonal transmission and 21% in putative plasmid-mediated dissemination events, particularly in abdominal surgery, geriatrics and septic orthopedics, often involving C. freundii harboring blaCTX-M-15, blaOXA-48/CTX-M-14b, and blaOXA-181 on IncHI2-IncHI2A, IncM1, and IncX3 plasmids, respectively.

conclusionsOur study highlights the role of C. freundii as a vector of both clonal and plasmid-mediated, nosocomial transmission of antimicrobial resistance. It emphasizes the need to include C. freundii in genomic and epidemiological surveillance to detect its silent spread.

Indexed as

Citrobacter freundiiCross InfectionDrug Resistance, Multiple, BacterialEnterobacteriaceae InfectionsAgedAged, 80 and overAnti-Bacterial Agentsbeta-LactamasesFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedMolecular EpidemiologyMultilocus Sequence TypingPlasmidsAnti-Bacterial Agentsbeta-LactamasesCitrobacter freundiihospital acquiredmolecular epidemiologymultidrug resistanceplasmid transmission

Identifiers

PMID41635259
PMCPMC13175611

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Registered trials

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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.