Evidence map›Paper›PMID 40740068›Full record

ArticleThe Journal of antimicrobial chemotherapy2025

Determination of epidemiological cut-off values for Narasin, Salinomycin, Lasalocid and Monensin in Enterococcus faecium.

Maria Laura Ferrando, Francesca Saluzzo, Rikki Franklin Frederiksen, Jannice Schau Slettemeås, Anne Margrete Urdahl, Roger Simm, Magdalena Skarżyńska, Magdalena Zając, Anna Lalak, Jowita Niczyporuk and 10 more

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 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. 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

20 authors.

Maria Laura FerrandoDivision Immunology, Transplant and Infectious Diseases, IRCCS Ospedale San Raffaele (OSR), Via Olgettina 60, Milan 20123, Italy.ORCID 0000-0002-1398-8244
Francesca SaluzzoDivision Immunology, Transplant and Infectious Diseases, IRCCS Ospedale San Raffaele (OSR), Via Olgettina 60, Milan 20123, Italy.ORCID 0000-0001-6705-1716
Rikki Franklin FrederiksenDepartment of Animal Health and Food Safety, Norwegian Veterinary Institute (NVI), P.O. Box 64, Ås 1431, Norway.
Jannice Schau SlettemeåsDepartment of Animal Health and Food Safety, Norwegian Veterinary Institute (NVI), P.O. Box 64, Ås 1431, Norway.
Anne Margrete UrdahlDepartment of Animal Health and Food Safety, Norwegian Veterinary Institute (NVI), P.O. Box 64, Ås 1431, Norway.
Roger SimmDepartment of Biosciences, University of Oslo, P.O. Box 1066, Blindern, Oslo 0316, Norway.
Magdalena SkarżyńskaDepartment of Microbiology, National Veterinary Research Institute (PIWet), Partyzantow Avenue 57, Pulawy 24-100, Poland.
Magdalena ZającDepartment of Microbiology, National Veterinary Research Institute (PIWet), Partyzantow Avenue 57, Pulawy 24-100, Poland.ORCID 0000-0002-8155-7614
Anna LalakDepartment of Microbiology, National Veterinary Research Institute (PIWet), Partyzantow Avenue 57, Pulawy 24-100, Poland.
Jowita NiczyporukDepartment of Microbiology, National Veterinary Research Institute (PIWet), Partyzantow Avenue 57, Pulawy 24-100, Poland.
Dariusz WasylDepartment of Microbiology, National Veterinary Research Institute (PIWet), Partyzantow Avenue 57, Pulawy 24-100, Poland.
Léa DuvalANSES, Ploufragan, Plouzané Niort laboratory, Mycoplasmology Bacteriology and Antimicrobial Unit (ANSES), Zoopole Les Croix, BP 53, Ploufragan 22440, France.
Florence TardyANSES, Ploufragan, Plouzané Niort laboratory, Mycoplasmology Bacteriology and Antimicrobial Unit (ANSES), Zoopole Les Croix, BP 53, Ploufragan 22440, France.
Claire SchapendonkWageningen University and Research, Wageningen Food Safety Research (WFSR), P.O. Box 230, Wageningen 6708 WB, The Netherlands.
Michel RapalliniWageningen University and Research, Wageningen Food Safety Research (WFSR), P.O. Box 230, Wageningen 6708 WB, The Netherlands.
Giovanni TosiIstituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia-Romagna (I.Z.S.L.E.R.), Forlì 47122, Italy.
Simona PerulliIstituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia-Romagna (I.Z.S.L.E.R.), Forlì 47122, Italy.
Letizia CirasellaIstituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia-Romagna (I.Z.S.L.E.R.), Forlì 47122, Italy.
Daniela Maria CirilloDivision Immunology, Transplant and Infectious Diseases, IRCCS Ospedale San Raffaele (OSR), Via Olgettina 60, Milan 20123, Italy.
Mariel G PikkemaatWageningen University and Research, Wageningen Food Safety Research (WFSR), P.O. Box 230, Wageningen 6708 WB, The Netherlands.

Funding

French National Research Agency ANR-21-AAMR-0004-02Italian Ministry of Health ERP-2021-23680703Joint Programming Initiative on Antimicrobial Resistance JPIAMR_2021_P010Netherlands Organization for Health Research and Development ZonMw 1070132110001Polish National Science Centre NCN 2021/03/Y/NZ7/00136Research Council of Norway 333858
6 · The paper itself

Abstract

objectivesTo establish epidemiological cut-off values (ECOFFs) for the polyether ionophores narasin, salinomycin, lasalocid and monensin in Enterococcus faecium.

methodsMICs were measured using the broth microdilution method according to ISO 20776-1 (2019). Method validation involved ≥10 replicates of antimicrobial susceptibility testing of Enterococcus faecalis ATCC 29212. A total of 182 E. faecium isolates from various sources were tested in five European laboratories. The ECOFFinder tool from EUCAST was used to establish the ECOFFs for 122 WT isolates, verified by PCR or WGS.

resultsMethod validation showed consistency, with acceptable variation within ±1 2-fold dilution. The ECOFF for narasin was 0.5 mg/L, considerably below the current EUCAST ECOFF for E. faecium (ECOFF = 2 mg/L). Salinomycin and lasalocid ECOFFs were 1 and 2 mg/L, respectively. Strains carrying the previously identified narAB resistance genes clearly manifested a separate MIC distribution for narasin and salinomycin, but not for lasalocid, although a clear bias to the higher MIC values within the normal distribution could be observed. Monensin apparently displayed a broader MIC range (0.5-64 mg/L) with multiple modes, which precluded the establishment of an ECOFF for monensin.

conclusionsThe study yielded novel ECOFFs for distinguishing WT E. faecium strains for the key veterinary ionophores, providing a mainstay for a better understanding of ionophore resistance in enterococci.

Indexed as

Anti-Bacterial AgentsEnterococcus faeciumGram-Positive Bacterial InfectionsIonophoresLasalocidMonensinAnimalsChickensDrug Resistance, BacterialEuropeMicrobial Sensitivity TestsPolyether PolyketidesPyransAnti-Bacterial AgentsIonophoresLasalocidMonensinnarasinPolyether PolyketidesPyranssalinomycin

Identifiers

PMID40740068
PMCPMC12404726

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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.