Evidence map›Paper›PMID 42207601›Full record

ArticleThe Journal of antimicrobial chemotherapy2026

Performance of EUCAST disc diffusion and supplementary methods to detect reduced susceptibility to linezolid in enterococci- the NordicAST LRE-study.

Bjørg Christina Haldorsen, Marita Helen Augustinussen, Erika Matuschek, Lars Småbrekke, Frode Skjold, Joachim Hegstad, Barbara Juliane Holzknecht, Kristján Orri Helgason, Heikki Ilmavirta, Gunnar Kahlmeter and 3 more

Abstract readMulticenter StudyEvaluation Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Bjørg Christina HaldorsenNorwegian Centre for Detection of Antimicrobial Resistance, Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.
Marita Helen AugustinussenNorwegian Centre for Detection of Antimicrobial Resistance, Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.
Erika MatuschekEUCAST Development Laboratory, Clinical Microbiology, Central Hospital, Växjö, Sweden.ORCID 0000-0001-8163-3667
Lars SmåbrekkeDepartment of Pharmacy, UiT the Arctic University of Norway, Tromsø, Norway.
Frode SkjoldDepartment of Pharmacy, UiT the Arctic University of Norway, Tromsø, Norway.
Joachim HegstadDepartment of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.
Barbara Juliane HolzknechtDepartment of Clinical Microbiology, Copenhagen University Hospital - Herlev and Gentofte, Herlev, Denmark.
Kristján Orri HelgasonDepartment of Clinical Microbiology, Landspitali University Hospital of Iceland, Reykjavik, Iceland.
Heikki IlmavirtaDepartment of Clinical Microbiology, University of Eastern Finland, Kuopio, Finland.
Gunnar KahlmeterEUCAST Development Laboratory, Clinical Microbiology, Central Hospital, Växjö, Sweden.
Arnfinn SundsfjordNorwegian Centre for Detection of Antimicrobial Resistance, Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.
Kristin HegstadNorwegian Centre for Detection of Antimicrobial Resistance, Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway.ORCID 0000-0002-1314-0497
NordicAST 2023 LRE-TRE Study Group

Funding

NordicAST networkNorthern Norway Regional Health Authority Medical Research Programme HNF1711-24
6 · The paper itself

Abstract

objectivesThis multicentre study aimed to assess performance of the EUCAST disc diffusion (DD) and MIC methods for linezolid susceptibility testing in a genetically diverse strain collection.

methodsNordic clinical microbiology laboratories (n = 83) were invited to test a blinded collection of well-characterized Enterococcus faecalis (n = 10) and Enterococcus faecium (n = 10) strains using the EUCAST DD and gradient tests [Etest and MIC Test strips (MTS)] from two manufacturers (bioMerieux and Liofilchem). Results were compared to reference broth microdilution (BMD) MICs and genotype (presence/absence of linezolid resistance determinants).

resultsForty-five laboratories provided DD, and 41 gradient test results. Comparing DD with reference MICs and genotype yielded overall categorical agreements (CA) of 87.0% and 97.8%, respectively. Essential agreement (EA) was 99.7% for Etest (bias +10.0%) and 84.5% for MTS (bias +71.0%). Susceptibility categorization with Etest and MTS showed CA of 90.5% and 84.1% with reference MICs, and 82.9% and 98.6% with genotype, respectively. Most discrepancies involved strains with borderline linezolid MICs (4-8 mg/L) and known linezolid resistance mechanisms. Linezolid exposure of strains with MIC 4 mg/L carrying transferable resistance genes (optrA or poxtA), led to MIC increasing above the clinical breakpoint.

conclusionsEtest and EUCAST DD had the highest CAs with linezolid reference MIC. EUCAST DD method and MTS gradient test consistently detected strains with confirmed resistance mechanisms. Our findings highlight the potential clinical implications of resistance determinants in MIC borderline strains and support the need for an area of technical uncertainty or a warning in breakpoint tables for linezolid in enterococci.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialEnterococcus faecalisEnterococcus faeciumLinezolidGenotypeHumansMicrobial Sensitivity TestsScandinavian and Nordic CountriesAnti-Bacterial AgentsLinezolid

Identifiers

PMID42207601
PMCPMC13218288

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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.