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Characterisation of Salmonella Typhimurium from a fatal equine nosocomial outbreak and retrospective analysis of equine clinic salmonellosis cases (2010–2025)
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  • Published: 18 February 2026

Characterisation of Salmonella Typhimurium from a fatal equine nosocomial outbreak and retrospective analysis of equine clinic salmonellosis cases (2010–2025)

  • Katalin K-Jánosi  ORCID: orcid.org/0009-0002-7440-16941,
  • Anita Sztojka1,
  • István Emil Kis1,
  • Imre Biksi1,
  • Zoltán Bakos2,
  • Eszter Kaszab3,4,5,
  • Tünde Mag6 &
  • …
  • Ervin Albert  ORCID: orcid.org/0000-0002-2244-75381,7 

Scientific Reports , Article number:  (2026) Cite this article

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Subjects

  • Diseases
  • Microbiology
  • Molecular biology

Abstract

In 2024, a highly fatal outbreak of equine salmonellosis occurred in a Hungarian equine referral hospital, resulting in the death or euthanasia of four out of five affected horses. Salmonella (S.) enterica subsp. enterica serovar Typhimurium was identified as the primary causative agent from equine faecal, reflux, and post-mortem intestinal content samples, while one case involved S. Coeln. Extensive environmental sampling during the outbreak also yielded multiple Salmonella serovars. Whole-genome sequencing revealed a high degree of genetic relatedness among the S. Typhimurium isolates, confirming nosocomial transmission. The source of the isolated S. Typhimurium was most likely a 3-year-old gelding imported immediately before the admission to the hospital. The isolates belonged to sequence type ST376 and exhibited multidrug resistance, including extended-spectrum β-lactamase and fluoroquinolone resistance genes. Retrospective analysis of microbiological records from 2010 to mid-2024 identified 23 Salmonella-positive equine cases involving eight serovars and three probable nosocomial clusters preceding the 2024 outbreak. Following the outbreak, enhanced passive surveillance was implemented between October 2024 and August 2025. During this period, 56 at-risk horses were examined using selective bacteriological testing of clinical and post-mortem samples, of which 11 (19.6%) were Salmonella-positive, representing eight different serovars. A distinct cluster of S. Martonos was detected, and six of the surveillance-associated cases resulted in fatal outcomes. These findings demonstrate that Salmonella is repeatedly introduced into the equine hospital environment and that serovars differ markedly in virulence and transmission dynamics. The exceptionally high case fatality observed during the 2024 outbreak underscores the importance of integrated genomic surveillance, rapid diagnostics, and sustained infection control measures to mitigate the risk of severe nosocomial salmonellosis in equine clinics.

Data availability

The datasets supporting the conclusions of this article are included within the article and its online additional files, and also available under the PRJNA1269797 (https://www.ncbi.nlm.nih.gov/sra/PRJNA1269797) BioProject accession number of the NCBI Sequence Read Archive database. Further data are available from the corresponding author on reasonable request.

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Acknowledgements

The authors thank Ms Edit Csuka and Ms Veronika Busa for their excellent technical assistance.

Funding

Open access funding provided by University of Veterinary Medicine. This research was funded by the National Research, Development, and Innovation Office (grant no., RRF-2.3.1–21-2022–00001).

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Authors and Affiliations

  1. Department of Pathology, University of Veterinary Medicine Budapest, Üllő, Hungary

    Katalin K-Jánosi, Anita Sztojka, István Emil Kis, Imre Biksi & Ervin Albert

  2. Department and Clinic of Equine Medicine, University of Veterinary Medicine Budapest, Üllő, Hungary

    Zoltán Bakos

  3. Department of Microbiology and Infectious Diseases, University of Veterinary Medicine Budapest, Budapest, Hungary

    Eszter Kaszab

  4. National Laboratory of Infectious Animal Diseases, Antimicrobial Resistance, Veterinary Public Health and Food Chain Safety, University of Veterinary Medicine Budapest, Budapest, Hungary

    Eszter Kaszab

  5. Faculty of Health Sciences, One Health Institute, University of Debrecen, Debrecen, Hungary

    Eszter Kaszab

  6. Department of Laboratory of Bacteriology, Mycology, and Parasitology, National Centre for Public Health and Pharmacy, Budapest, Hungary

    Tünde Mag

  7. Centre for Metagenomics, Multidisciplinary Health Industry Coordination Institute, University of Debrecen, Debrecen, Hungary

    Ervin Albert

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Contributions

EA, IB, IEK: pathological, histopathological, bacteriological examinations. ZB: collection and summarising patient data and clinical records. AS: retrospective data collection. EK, TM: molecular genomic investigations. EA, KKJ: summarising and analysing raw data; text elaboration of the manuscript; interpretation of materials and methods, results, discussion and conclusions. EA, IB: supervision of the activities. ZB, IEK, AS: internal review of the manuscript. The authors read and approved the final manuscript.

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Correspondence to Katalin K-Jánosi.

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The cadavers were referred to the Livestock Diagnostic Centre (Department of Pathology, University of Veterinary Medicine Budapest, Üllő, Hungary) for laboratory diagnostics. All the investigations were performed on deceased animals and organs of them, therefore ethics approval and a consent to participate are not applicable, as well as no protocol approval of any ethical committee was required. Informed consent was received from all animal owners.

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K-Jánosi, K., Sztojka, A., Kis, I.E. et al. Characterisation of Salmonella Typhimurium from a fatal equine nosocomial outbreak and retrospective analysis of equine clinic salmonellosis cases (2010–2025). Sci Rep (2026). https://doi.org/10.1038/s41598-026-40617-0

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  • Received: 31 October 2025

  • Accepted: 13 February 2026

  • Published: 18 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-40617-0

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Keywords

  • Equine
  • Salmonellosis
  • High case fatality
  • Salmonella Typhimurium
  • ESBL
  • WGS
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