Analyze Diet
Pathogens (Basel, Switzerland)2021; 10(5); 537; doi: 10.3390/pathogens10050537

Apparent Breed Predilection for Equid Herpesvirus-1-Associated Myeloencephalopathy (EHM) in a Multiple-Breed Herd.

Abstract: Equid herpesvirus type 1 (EHV-1) causes several outbreaks of abortion and/or equid herpesvirus-associated myeloencephalopathy (EHM) worldwide each year. EHM is of great concern, as permanent neurological gait anomalies can leave a horse unfit for future use. The study assesses the risk factors associated with the occurrence of EHM. During an unmitigated outbreak, 141 adult horses/ponies of several distinct breeds were evaluated-using multiple Bayesian logistic regression calculating the odds ratios for breed, age, and sex. In total, 33 of the 141 horses showed signs of EHM. Fjord horses and warmblood horses were overrepresented among those developing EHM. The pony breeds, Welsh and Shetland ponies, were underrepresented. In addition, age and sex were not associated with the risk for EHM. The main limitation was that it was a retrospective analysis with some flaws of documentation. It can be concluded that breed was a significant risk factor for developing EHM during this outbreak.
Publication Date: 2021-04-29 PubMed ID: 33947126PubMed Central: PMC8145278DOI: 10.3390/pathogens10050537Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research studies the factors contributing to the occurrence of Equid Herpesvirus-1-Associated Myeloencephalopathy (EHM) in horses, revealing that breed holds significance, whereas age and sex do not.

Understanding Equid Herpesvirus-1

  • Equid herpesvirus type 1 (EHV-1) is an infectious virus causing multiple outbreaks every year among equine populations.
  • Evidence of this virus often consists of instances of abortion or neurologic disease, known as Equid Herpesvirus-associated myeloencephalopathy (EHM).
  • EHM poses a significant threat because it can cause lasting alterations in a horse’s gait—often leaving them unfit for future use.

Purpose of the Study

  • The purpose of this research was to identify the risk factors associated with the development of EHM.
  • The researchers wanted to understand whether variables like breed, age, and sex could impact a horse’s susceptibility to EHM.

Research Methods

  • This study’s process involved an examination of 141 adult horses/ponies of various distinct breeds during an active outbreak.
  • Breed, age, and sex were analyzed via Bayesian logistic regression to compute the odds ratios and identify potential correlating factors with the occurrence of EHM.

Findings

  • Of the total 141 horses examined, 33 showed signs of EHM.
  • The results pointed to breed as a significant factor linked to developing EHM, with Fjord horses and warmblood horses being overrepresented.
  • Similarly, the study found Welsh and Shetland pony breeds to be underrepresented among the afflicted, further suggesting a link between breed and disease susceptibility.
  • On the contrary, the study found no substantial correlation between a horse’s age or sex and the risk of developing EHM.

Limitations and Conclusion

  • One of the main limitations highlighted in the study was its retrospective nature, which might have led to certain flaws in documentation.
  • Despite this, the study concluded that breed presents a significant risk factor in the emergence of EHM during outbreaks of EHV-1.

Cite This Article

APA
Klouth E, Zablotski Y, Goehring LS. (2021). Apparent Breed Predilection for Equid Herpesvirus-1-Associated Myeloencephalopathy (EHM) in a Multiple-Breed Herd. Pathogens, 10(5), 537. https://doi.org/10.3390/pathogens10050537

Publication

ISSN: 2076-0817
NlmUniqueID: 101596317
Country: Switzerland
Language: English
Volume: 10
Issue: 5
PII: 537

Researcher Affiliations

Klouth, Eva
  • Equine Hospital Center for Clinical Veterinary Medicine, Faculty of Veterinary Medicine Ludwig-Maximilians University, 80539 Munich, Germany.
Zablotski, Yury
  • Center for Clinical Veterinary Medicine, Faculty of Veterinary Medicine Ludwig-Maximilians University, 80539 Munich, Germany.
Goehring, Lutz S
  • Equine Hospital Center for Clinical Veterinary Medicine, Faculty of Veterinary Medicine Ludwig-Maximilians University, 80539 Munich, Germany.

Grant Funding

  • LMU-54772-2 / Dechra Veterinary Products

Conflict of Interest Statement

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

This article includes 15 references
  1. Allen GP. Risk factors for development of neurologic disease after experimental exposure to equine herpesvirus-1 in horses.. Am J Vet Res 2008 Dec;69(12):1595-600.
    doi: 10.2460/ajvr.69.12.1595pubmed: 19046006google scholar: lookup
  2. Goehring LS, van Winden SC, van Maanen C, Sloet van Oldruitenborgh-Oosterbaan MM. Equine herpesvirus type 1-associated myeloencephalopathy in The Netherlands: a four-year retrospective study (1999-2003).. J Vet Intern Med 2006 May-Jun;20(3):601-7.
  3. Allen GP, Kydd JH, Slater JD, Smith KC. Advances in understanding of the pathogenesis, epidemiology and immunological control of equine herpesvirus abortion.. Equine Infectious Diseases 8th ed. R&W Publications; Newmarket, UK: 1999. pp. 129–146.
  4. Henninger RW, Reed SM, Saville WJ, Allen GP, Hass GF, Kohn CW, Sofaly C. Outbreak of neurologic disease caused by equine herpesvirus-1 at a university equestrian center.. J Vet Intern Med 2007 Jan-Feb;21(1):157-65.
  5. Traub-Dargatz JL, Pelzel-McCluskey AM, Creekmore LH, Geiser-Novotny S, Kasari TR, Wiedenheft AM, Bush EJ, Bjork KE. Case-control study of a multistate equine herpesvirus myeloencephalopathy outbreak.. J Vet Intern Med 2013 Mar-Apr;27(2):339-46.
    doi: 10.1111/jvim.12051pubmed: 23398291google scholar: lookup
  6. Nugent J, Birch-Machin I, Smith KC, Mumford JA, Swann Z, Newton JR, Bowden RJ, Allen GP, Davis-Poynter N. Analysis of equid herpesvirus 1 strain variation reveals a point mutation of the DNA polymerase strongly associated with neuropathogenic versus nonneuropathogenic disease outbreaks.. J Virol 2006 Apr;80(8):4047-60.
  7. Bürki F, Nowotny N, Hinaidy B, Pallan C. Die Ätiologie der Lipizzanerseuche in Piber 1983: Equine Herpesvirus 1. Wien Tierärztl Mschr 1984;71:312–320.
  8. Bitsch V, Dam A. Nervous disturbances in horses in relation to infection with equine rhinopneumonitis virus.. Acta Vet Scand 1971;12(1):134-6.
    pubmed: 4324962
  9. Greenwood RE, Simson AR. Clinical report of a paralytic syndrome affecting stallions, mares and foals on a thoroughbred studfarm.. Equine Vet J 1980 Jul;12(3):113-7.
  10. Carman S, Nagy E, Caldwell D, van Dreumel TA. Equine herpesvirus type 1 neurological disease and enterocolitis in mature standardbred horses.. J Vet Diagn Invest 1993 Apr;5(2):261-5.
    doi: 10.1177/104063879300500221pubmed: 8389601google scholar: lookup
  11. Friday PA, Scarratt WK, Elvinger F, Timoney PJ, Bonda A. Ataxia and paresis with equine herpesvirus type 1 infection in a herd of riding school horses.. J Vet Intern Med 2000 Mar-Apr;14(2):197-201.
  12. van Maanen C, Sloet van Oldruitenborgh-Oosterbaan MM, Damen EA, Derksen AG. Neurological disease associated with EHV-1-infection in a riding school: clinical and virological characteristics.. Equine Vet J 2001 Mar;33(2):191-6.
  13. Khanshour A, Conant E, Juras R, Cothran EG. Microsatellite analysis of genetic diversity and population structure of Arabian horse populations.. J Hered 2013 May-Jun;104(3):386-98.
    doi: 10.1093/jhered/est003pubmed: 23450090google scholar: lookup
  14. Sadeghi R, Moradi-Shahrbabak M, Miraei Ashtiani SR, Schlamp F, Cosgrove EJ, Antczak DF. Genetic Diversity of Persian Arabian Horses and Their Relationship to Other Native Iranian Horse Breeds.. J Hered 2019 Mar 5;110(2):173-182.
    doi: 10.1093/jhered/esy061pubmed: 30590570google scholar: lookup
  15. . EQUINE RHINOPNEUMONITIS—SPAIN (02): (VALENCIA) EHV-1, HORSE, INTERNATIONAL SPREAD, CONTROL. ProMED (accessed on 14 March 2021).

Citations

This article has been cited 4 times.
  1. Klouth E, Zablotski Y, Petersen JL, de Bruijn M, Gröndahl G, Müller S, Goehring LS. Epidemiological Aspects of Equid Herpesvirus-Associated Myeloencephalopathy (EHM) Outbreaks.. Viruses 2022 Nov 21;14(11).
    doi: 10.3390/v14112576pubmed: 36423188google scholar: lookup
  2. Thieulent CJ, Sutton G, Toquet MP, Fremaux S, Hue E, Fortier C, Pléau A, Deslis A, Abrioux S, Guitton E, Pronost S, Paillot R. Oral Administration of Valganciclovir Reduces Clinical Signs, Virus Shedding and Cell-Associated Viremia in Ponies Experimentally Infected with the Equid Herpesvirus-1 C(2254) Variant.. Pathogens 2022 May 4;11(5).
    doi: 10.3390/pathogens11050539pubmed: 35631060google scholar: lookup
  3. Hu Y, Jia Q, Liu J, Sun W, Bao Z, Che C, Wu G, Fan B, Jarhen, Ran D. Molecular characteristics and pathogenicity of an equid alphaherpesvirus 1 strain isolated in China.. Virus Genes 2022 Aug;58(4):284-293.
    doi: 10.1007/s11262-022-01910-ypubmed: 35567668google scholar: lookup
  4. Nielsen SS, Alvarez J, Bicout DJ, Calistri P, Canali E, Drewe JA, Garin-Bastuji B, Gonzales Rojas JL, Gortázar C, Herskin M, Michel V, Miranda Chueca MÁ, Roberts HC, Padalino B, Pasquali P, Spoolder H, Ståhl K, Calvo AV, Viltrop A, Winckler C, Carvelli A, Paillot R, Broglia A, Kohnle L, Baldinelli F, Van der Stede Y. Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): infection with Equine Herpesvirus-1.. EFSA J 2022 Jan;20(1):e07036.
    doi: 10.2903/j.efsa.2022.7036pubmed: 35035581google scholar: lookup