Evidence map›Paper›PMID 39450288›Full record

ArticleFrontiers in microbiology2024

Towards harmonized laboratory methodologies in veterinary clinical bacteriology: outcomes of a European survey.

Tom Koritnik, Iskra Cvetkovikj, Flavia Zendri, Shlomo Eduardo Blum, Serafeim Christos Chaintoutis, Peter A Kopp, Cassia Hare, Zrinka Štritof, Sonja Kittl, José Gonçalves and 8 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Veterinary Clinics as Reservoirs forAntibiotics (Basel, Switzerland) · 2025
    Review
  4. EAVLD 2024 - 7Italian journal of food safety · 2024
    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

18 authors.

Tom Koritnik *Department for Public Health Microbiology Ljubljana, Centre for Medical Microbiology, National Laboratory of Health, Environment and Food, Ljubljana, Slovenia.
Iskra Cvetkovikj *Department of Microbiology and Immunology, Faculty of Veterinary medicine-Skopje, Ss Cyril and Methodius University in Skopje, Skopje, Republic of North Macedonia.
Flavia ZendriDepartment of Veterinary Anatomy, Physiology and Pathology, Institute of Infection, Veterinary and Ecological Sciences, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Shlomo Eduardo BlumDepartment of Bacteriology and Mycology, Kimron Veterinary Institute, Bet Dagan, Israel.
Serafeim Christos ChaintoutisDiagnostic Laboratory, School of Veterinary Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Peter A KoppIDEXX Vet Med Labor GmbH, Kornwestheim, Germany.
Cassia HareDepartment of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
Zrinka ŠtritofDepartment of Microbiology and Infectious Diseases with Clinic, Faculty of Veterinary Medicine, University of Zagreb, Zagreb, Croatia.
Sonja KittlDepartment of Infectious Diseases and Pathobiology, Institute of Veterinary Bacteriology, University of Bern, Bern, Switzerland.
José GonçalvesMARE-Marine and Environmental Sciences Centre, ARNET-Aquatic Research Network Associate Laboratory, NOVA School of Science and Technology, NOVA University Lisbon, Caparica, Portugal.
Irena ZdovcVeterinary Faculty of Ljubljana, Institute of Microbiology and Parasitology, Ljubljana, Slovenia.
Erik PaulshusDepartment of Analysis and Diagnostics, Microbiology, Norwegian Veterinary Institute, Ås, Norway.
Andrea LaconiDepartment of Comparative Biomedicine and Food Science, University of Padua, Legnaro, Italy.
David SingletonDepartment of Veterinary Anatomy, Physiology and Pathology, Institute of Infection, Veterinary and Ecological Sciences, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.
Fergus AllertonWillows Veterinary Centre and Referral Service, Shirley, United Kingdom.
Els M BroensESCMID Study Group for Veterinary Microbiology (ESGVM), Basel, Switzerland.
Peter DamborgESCMID Study Group for Veterinary Microbiology (ESGVM), Basel, Switzerland.
Dorina TimofteDepartment of Veterinary Anatomy, Physiology and Pathology, Institute of Infection, Veterinary and Ecological Sciences, School of Veterinary Science, Leahurst Campus, University of Liverpool, Neston, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Veterinary clinical microbiology laboratories play a key role in antimicrobial stewardship, surveillance of antimicrobial resistance and prevention of healthcare associated-infections. However, there is a shortage of international harmonized guidelines covering all steps of veterinary bacterial culture from sample receipt to reporting. Methods: In order to gain insights, the European Network for Optimization of Veterinary Antimicrobial Treatment (ENOVAT) designed an online survey focused on the practices and interpretive criteria used for bacterial culture and identification (C&ID), and antimicrobial susceptibility testing (AST) of animal bacterial pathogens. Results: A total of 241 microbiology laboratories in 34 European countries completed the survey, representing a mixture of academic (37.6%), governmental (27.4%), and private (26.5%) laboratories. The C&ID turnaround varied from 1 to 2 days (77.8%) to 3-5 days (20%), and 6- 8 days (1.6%), with similar timeframes for AST. Individual biochemical tests and analytical profile index (API) biochemical test kits or similar were the most frequent tools used for bacterial identification (77% and 56.2%, respectively), followed by PCR (46.6%) and MALDI-TOF MS (43.3%). For AST, Kirby-Bauer disk diffusion (DD) and minimum inhibitory concentration (MIC) determination were conducted by 43.8% and 32.6% of laboratories, respectively, with a combination of EUCAST and CLSI clinical breakpoints (CBPs) preferred for interpretation of the DD (41.2%) and MIC (47.6%) results. In the absence of specific CBPs, laboratories used human CBPs (53.3%) or veterinary CBPs representing another body site, organism or animal species (51.5%). Importantly, most laboratories (47.9%) only report the qualitative interpretation of the result (S, R, and I). As regards testing for AMR mechanisms, 48.5% and 46.7% of laboratories routinely screened isolates for methicillin resistance and ESBL production, respectively. Notably, selective reporting of AST results (i.e. excluding highest priority critically important antimicrobials from AST reports) was adopted by 39.5% of laboratories despite a similar proportion not taking any approach (37.6%) to guide clinicians towards narrower-spectrum or first-line antibiotics. Discussion: In conclusion, we identified a broad variety of methodologies and interpretative criteria used for C&ID and AST in European veterinary microbiological diagnostic laboratories. The observed gaps in veterinary microbiology practices emphasize a need to improve and harmonize professional training, innovation, bacterial culture methods and interpretation, AMR surveillance and reporting strategies.

Indexed as

antimicrobial susceptibility testingbacterial culturebacterial identificationENOVATharmonizationmethodologiesveterinary clinical bacteriology

Identifiers

PMID39450288
PMCPMC11499178

What OpenQuestion holds

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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.