Evidence map›Paper›PMID 40872247›Full record

ArticlePathogens (Basel, Switzerland)2025

Outbreak Caused by VIM-1- and VIM-4-Positive

Branka Bedenić, Gernot Zarfel, Josefa Luxner, Andrea Grisold, Marina Nađ, Maja Anušić, Vladimira Tičić, Verena Dobretzberger, Ivan Barišić, Jasmina Vraneš

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Tackling Drug Resistance and Virulence inThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2026
    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

10 authors.

Branka BedenićBiomedical Research Institute-BIMIS, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Gernot ZarfelDiagnostic and Research Institute for Hygiene, Microbiology and Environmental Medicine, Medical University Graz, 8010 Graz, Austria.ORCID 0000-0003-1592-4559
Josefa LuxnerDiagnostic and Research Institute for Hygiene, Microbiology and Environmental Medicine, Medical University Graz, 8010 Graz, Austria.ORCID 0009-0002-6579-5089
Andrea GrisoldDiagnostic and Research Institute for Hygiene, Microbiology and Environmental Medicine, Medical University Graz, 8010 Graz, Austria.ORCID 0000-0002-6937-521X
Marina NađUniversity of Zagreb School of Medicine,10000 Zagreb, Croatia.
Maja AnušićDepartment of Clinical Microbiology, Dr Andrija Štampar Teaching Institute of Public Health Zagreb, 10000 Zagreb, Croatia.
Vladimira TičićDepartment of Clinical Microbiology, Dr Andrija Štampar Teaching Institute of Public Health Zagreb, 10000 Zagreb, Croatia.
Verena DobretzbergerDepartment of Molecular Diagnostics, Austrian Institute for Technology, 1210 Vienna, Austria.ORCID 0000-0003-2365-8975
Ivan BarišićDepartment of Molecular Diagnostics, Austrian Institute for Technology, 1210 Vienna, Austria.ORCID 0000-0002-1301-6197
Jasmina VranešDepartment of Clinical Microbiology, Dr Andrija Štampar Teaching Institute of Public Health Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0002-3282-0973

Funding

University of Zagreb School of Medicine 10106-24-1294
6 · The paper itself

Abstract

BACKGROUND/

objectivesMATERIALS AND

methodsThe antibiotic susceptibility testing was performed by the disk-diffusion and broth dilution methods. The double-disk synergy test (DDST) and inhibitor-based test with clavulanic and phenylboronic acid were applied to screen for ESBLs and p-AmpCs, respectively. Carbapenemases were screened by the modified Hodge test (MHT), while carbapenem hydrolysis was investigated by the carbapenem inactivation method (CIM) and EDTA-carbapenem-inactivation method (eCIM). The nature of the ESBLs, carbapenemases, and fluoroquinolone-resistance determinants was investigated by PCR. Plasmids were characterized by PCR-based replicon typing (PBRT). Selected isolates were subjected to molecular characterization of the resistome by an Inter-Array Genotyping Kit CarbaResisit and whole-genome sequencing (WGS).

resultsIn total, 20 isolates were collected and analyzed. All isolates exhibited resistance to amoxicillin alone and when combined with clavulanic acid, cefuroxime, cefotaxime, ceftriaxone, cefepime, imipenem, ceftazidime-avibactam, ceftolozane-tazobactam, gentamicin, amikacin, and ciprofloxacin. There was uniform susceptibility to ertapenem, meropenem, and cefiderocol. The DDST and combined disk test with clavulanic acid were positive, indicating the production of an ESBL. The MHT was negative in all except one isolate, while the CIM showed moderate sensitivity, but only with imipenem as the indicator disk. Furthermore, eCIM tested positive in all of the CIM-positive isolates, consistent with a metallo-β-lactamase (MBL). PCR and sequencing of the selected amplicons identified VIM-1 and VIM-4. The Inter-Array Genotyping Kit CarbaResist and WGS identified β-lactam resistance genes

conclusionsThis study revealed an epidemic spread of carbapenemase-producing

Indexed as

beta-LactamasesCross InfectionDisease OutbreaksProteus InfectionsProteus mirabilisAnti-Bacterial AgentsBacterial ProteinsCroatiaDrug Resistance, Multiple, BacterialFemaleHospitalsHumansMaleMicrobial Sensitivity TestsMiddle AgedAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesVIM-1 metallo-beta-lactamaseCTX-M-15epidemic spreadmultidrug resistanceProteus mirabilisVIM

Identifiers

PMID40872247
PMCPMC12389321

What OpenQuestion holds

Textmetadata
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.