Misidentification of Raoultella spp. (R. terrigena, R. planticola) and Klebsiella spp. (K. variicola, K. grimontii) as Klebsiella pneumoniae: Retrospective study of a necropsy-associated bacterial collection from horses.
Abstract: Misidentifications as Klebsiella pneumoniae were observed during a French retrospective study of a necropsy-associated K. pneumoniae bacterial collection from horses. Accordingly, the present study aimed to further characterise the 12 Raoultella spp. and Klebsiella spp. strains involved in these misidentifications. The strains were identified and characterised using the Api 20E system, K. pneumoniae PCR detection, matrix-assisted laser desorption/ionisation time-of-flight mass spectroscopy and whole-genome sequencing. Antimicrobial susceptibilities were tested by the disc diffusion method with a panel of 40 antibiotics. Thus, misidentifications as K. pneumoniae mainly concerned Raoultella spp. (R. terrigena, R. planticola) rather than Klebsiella spp. (K. variicola, K. grimontii), with a dominance of R. terrigena. Among the 12 strains, only K. grimontii was multi-drug resistant and none were considered hypervirulent. MALDI-TOF was sufficient to avoid misidentification but commercial spectra databases should be expanded with K. grimontii and R. terrigena reference spectra to improve identification accuracy. This is probably (i) the first report of K. grimontii and R. planticola isolations from horses and (ii) the second report of R. terrigena and K. variicola isolations from horses.
Copyright © 2025 The Authors. Published by Elsevier B.V. All rights reserved.
Publication Date: 2025-03-28 PubMed ID: 40156970DOI: 10.1016/j.vetmic.2025.110497Google Scholar: Lookup
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Summary
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This research paper focuses on studying the misidentification of bacterial strains – primarily Raoultella and Klebsiella species – as Klebsiella pneumoniae within a collection obtained from horse autopsies.
Objective of the Study
- The main objective is to better understand the 12 Raoultella and Klebsiella strains involved in this misidentification process during the study.
Methods used in the Research
- The strains were identified using several technical methods, including the Api 20E system, detection via K. pneumoniae PCR, matrix-assisted laser desorption/ionisation time-of-flight mass spectroscopy (MALDI-TOF), and whole-genome sequencing.
Testing of Antimicrobial Susceptibilities
- The research went further by testing the strains’ antimicrobial susceptibilities using the disc diffusion method, involving a panel of 40 antibiotics.
Key Findings
- The main misidentifications concern Raoultella species (specifically, R. terrigena and R. planticola) as K. pneumoniae, rather than Klebsiella species (specifically, K. variicola and K. grimontii), with R. terrigena being the dominant strain.
- Among the 12 strains, it was found that only K. grimontii was multi-drug resistant, and none of the other strains were identified as hypervirulent.
- MALDI-TOF was found to be a reliable method to avoid such misidentification, however, the researchers suggest expanding commercial spectrum databases with K. grimontii and R. terrigena reference spectra to enhance the accuracy of the identification process.
- The research provides the first report of K. grimontii and R. planticola isolations from horses, as well as the second report of R. terrigena and K. variicola isolations from horses.
Cite This Article
APA
Gravey F, Sévin C, Langlois B, Maillard K, Foucher N, Duquesne F, Léon A, Le Hello S, Petry S.
(2025).
Misidentification of Raoultella spp. (R. terrigena, R. planticola) and Klebsiella spp. (K. variicola, K. grimontii) as Klebsiella pneumoniae: Retrospective study of a necropsy-associated bacterial collection from horses.
Vet Microbiol, 304, 110497.
https://doi.org/10.1016/j.vetmic.2025.110497 Publication
Researcher Affiliations
- Université de Caen Normandie, Université de Rouen Normandie, INSERM, DYNAMICURE UMR1311, CHU Caen, Department of Infectious Agents, Bacteriology, Caen 14000, France; CHU Caen, Department of Infectious Agents, Bacteriology, Caen 14000, France.
- ANSES, Normandy Laboratory for Animal Health, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
- Université de Caen Normandie, Université de Rouen Normandie, INSERM, DYNAMICURE UMR1311, CHU Caen, Department of Infectious Agents, Bacteriology, Caen 14000, France.
- LABÉO, Research Department, Caen, France.
- ANSES, Normandy Laboratory for Animal Health, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
- ANSES, Normandy Laboratory for Animal Health, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
- LABÉO, Research Department, Caen, France.
- Université de Caen Normandie, Université de Rouen Normandie, INSERM, DYNAMICURE UMR1311, CHU Caen, Department of Infectious Agents, Bacteriology, Caen 14000, France; CHU Caen, Department of Infectious Agents, Bacteriology, Caen 14000, France.
- ANSES, Normandy Laboratory for Animal Health, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France. Electronic address: sandrine.petry@anses.fr.
Conflict of Interest Statement
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper.
Citations
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