Analyze Diet
Veterinary microbiology2010; 149(3-4); 456-460; doi: 10.1016/j.vetmic.2010.11.024

Fatal epizootic equine herpesvirus 1 infections in new and unnatural hosts.

Abstract: In a zoological collection, four black bears (Ursus americanus) died from neurological disease within six months. Independently in a geographically different zoo, two Thomson's gazelles (Eudorcas thomsoni) and 18 guinea pigs (Cavia porcellus f. dom.) suffered from neurological disorders. In addition, guinea pigs showed abortions and stillbirths. All affected animals displayed a non suppurative meningoencephalitis with intranuclear inclusion bodies. Immunohistology demonstrated equine herpes virus antigen and ultrastructurally herpes viral particles were detected. Virus isolation and molecular analysis identified neurotropic equine herpesvirus (EHV) 1 strains in both epizootics. There is serological evidence of a possible virus transmission from other equids to the affected animals. Cross-species transmission of EHV-1 should be considered in the management of captive wild equids and ungulates, particularly with respect to fatal disease in irreplaceable species.
Publication Date: 2010-11-24 PubMed ID: 21167662DOI: 10.1016/j.vetmic.2010.11.024Google 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.

The research article discusses a case where four black bears, two Thomson’s gazelles and 18 guinea pigs developed neurological disorders and died due to an infection by a strain of the equine herpesvirus. There is a possibility that these animals contracted the virus from other equids, urging a need for better management of captive wild equids and ungulates to prevent such cross-species transmission in future.

Detailed Overview

  • The research began with an observation of unusual deaths in a zoological collection where four black bears died from a neurological disease over a span of six months. Separately, in a different zoo, the same neurological disorders were found in two Thomson’s gazelles and 18 guinea pigs. Along with the neurological diseases, the guinea pigs also showed symptoms of abortions and stillbirths.
  • All of the affected animals exhibited non-purulent meningoencephalitis, an inflammation of the brain, along with intranuclear inclusion bodies, which are irregularities found in the nucleus of a cell typically during viral infections.
  • After conducting immunohistological studies (a method to detect antigens in cells of a tissue), the researchers discovered the antigen of equine herpes virus in the affected animals, indicating that they were infected by this virus. Confirmation of this was further obtained through ultrastructural studies, where the virus particles were visually spotted.
  • The isolated virus from these animals was subjected to molecular analysis. The results indicated that it was a neurotropic strain of the equine herpesvirus (EHV) 1 behind both the outbreaks or epizootics. ‘Neurotropic’ refers to viruses that are capable of infecting nerve cells.
  • Upon serological examination (a test done to identify antibodies in a patient’s blood), there were indications that the virus transmission might have happened from other equids (a family of mammals that includes horses and zebras) to the animals that were affected.
  • In conclusion, the researchers suggest the consideration of possible cross-specic transmission of EHV-1 in the management of captive wild equids and ungulates (hooved mammals). This is particularly important to prevent fatal diseases in irreplaceable or endangered species.

Cite This Article

APA
Wohlsein P, Lehmbecker A, Spitzbarth I, Algermissen D, Baumgärtner W, Böer M, Kummrow M, Haas L, Grummer B. (2010). Fatal epizootic equine herpesvirus 1 infections in new and unnatural hosts. Vet Microbiol, 149(3-4), 456-460. https://doi.org/10.1016/j.vetmic.2010.11.024

Publication

ISSN: 1873-2542
NlmUniqueID: 7705469
Country: Netherlands
Language: English
Volume: 149
Issue: 3-4
Pages: 456-460

Researcher Affiliations

Wohlsein, Peter
  • Department of Pathology, University of Veterinary Medicine, Bünteweg 17, D-30559 Hannover, Germany. Peter.Wohlsein@tiho-hannover.de
Lehmbecker, Annika
    Spitzbarth, Ingo
      Algermissen, Dorothee
        Baumgärtner, Wolfgang
          Böer, Michael
            Kummrow, Maja
              Haas, Ludwig
                Grummer, Beatrice

                  MeSH Terms

                  • Animals
                  • Animals, Zoo / virology
                  • Antelopes / virology
                  • Base Sequence
                  • Cells, Cultured
                  • Female
                  • Guinea Pigs / virology
                  • Herpesviridae Infections / pathology
                  • Herpesviridae Infections / transmission
                  • Herpesviridae Infections / veterinary
                  • Herpesviridae Infections / virology
                  • Herpesvirus 1, Equid / isolation & purification
                  • Herpesvirus 1, Equid / pathogenicity
                  • Host Specificity
                  • Male
                  • Meningoencephalitis / pathology
                  • Meningoencephalitis / virology
                  • Molecular Sequence Data
                  • Pregnancy
                  • Pregnancy Complications, Infectious / virology
                  • Ursidae / virology

                  Citations

                  This article has been cited 17 times.
                  1. 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
                  2. Greenfield JB, Anderson MV, Dorey EA, Redman E, Gilleard JS, Nemeth NM, Rothenburger JL. Molecular characterization of Sarcocystis spp. as a cause of protozoal encephalitis in a free-ranging black bear. J Vet Diagn Invest 2022 Jan;34(1):146-152.
                    doi: 10.1177/10406387211038389pubmed: 34416834google scholar: lookup
                  3. Dayaram A, Seeber PA, Greenwood AD. Environmental Detection and Potential Transmission of Equine Herpesviruses. Pathogens 2021 Apr 1;10(4).
                    doi: 10.3390/pathogens10040423pubmed: 33916280google scholar: lookup
                  4. Alex CE, Fahsbender E, Altan E, Bildfell R, Wolff P, Jin L, Black W, Jackson K, Woods L, Munk B, Tse T, Delwart E, Pesavento PA. Viruses in unexplained encephalitis cases in American black bears (Ursus americanus). PLoS One 2020;15(12):e0244056.
                    doi: 10.1371/journal.pone.0244056pubmed: 33332429google scholar: lookup
                  5. Sutton G, Thieulent C, Fortier C, Hue ES, Marcillaud-Pitel C, Pléau A, Deslis A, Guitton E, Paillot R, Pronost S. Identification of a New Equid Herpesvirus 1 DNA Polymerase (ORF30) Genotype with the Isolation of a C(2254)/H(752) Strain in French Horses Showing no Major Impact on the Strain Behaviour. Viruses 2020 Oct 13;12(10).
                    doi: 10.3390/v12101160pubmed: 33066315google scholar: lookup
                  6. Sutton G, Garvey M, Cullinane A, Jourdan M, Fortier C, Moreau P, Foursin M, Gryspeerdt A, Maisonnier V, Marcillaud-Pitel C, Legrand L, Paillot R, Pronost S. Molecular Surveillance of EHV-1 Strains Circulating in France during and after the Major 2009 Outbreak in Normandy Involving Respiratory Infection, Neurological Disorder, and Abortion. Viruses 2019 Oct 4;11(10).
                    doi: 10.3390/v11100916pubmed: 31590336google scholar: lookup
                  7. Seeber PA, Dayaram A, Sicks F, Osterrieder N, Franz M, Greenwood AD. Noninvasive Detection of Equid Herpesviruses in Fecal Samples. Appl Environ Microbiol 2019 Feb 1;85(3).
                    doi: 10.1128/AEM.02234-18pubmed: 30446563google scholar: lookup
                  8. Seeber PA, Quintard B, Sicks F, Dehnhard M, Greenwood AD, Franz M. Environmental stressors may cause equine herpesvirus reactivation in captive Grévy's zebras (Equus grevyi). PeerJ 2018;6:e5422.
                    doi: 10.7717/peerj.5422pubmed: 30155350google scholar: lookup
                  9. Garvey M, Suárez NM, Kerr K, Hector R, Moloney-Quinn L, Arkins S, Davison AJ, Cullinane A. Equid herpesvirus 8: Complete genome sequence and association with abortion in mares. PLoS One 2018;13(2):e0192301.
                    doi: 10.1371/journal.pone.0192301pubmed: 29414990google scholar: lookup
                  10. Bello A, Frei S, Peters M, Balkema-Buschmann A, Baumgärtner W, Wohlsein P. Spontaneous diseases in captive ratites (Struthioniformes) in northwestern Germany: A retrospective study. PLoS One 2017;12(4):e0173873.
                    doi: 10.1371/journal.pone.0173873pubmed: 28403205google scholar: lookup
                  11. Abdelgawad A, Damiani A, Ho SY, Strauss G, Szentiks CA, East ML, Osterrieder N, Greenwood AD. Zebra Alphaherpesviruses (EHV-1 and EHV-9): Genetic Diversity, Latency and Co-Infections. Viruses 2016 Sep 20;8(9).
                    doi: 10.3390/v8090262pubmed: 27657113google scholar: lookup
                  12. Abdelgawad A, Hermes R, Damiani A, Lamglait B, Czirják GÁ, East M, Aschenborn O, Wenker C, Kasem S, Osterrieder N, Greenwood AD. Comprehensive Serology Based on a Peptide ELISA to Assess the Prevalence of Closely Related Equine Herpesviruses in Zoo and Wild Animals. PLoS One 2015;10(9):e0138370.
                    doi: 10.1371/journal.pone.0138370pubmed: 26378452google scholar: lookup
                  13. Rebelo AR, Carman S, Shapiro J, van Dreumel T, Hazlett M, Nagy É. Equid herpesvirus 9 (EHV-9) isolates from zebras in Ontario, Canada, 1989 to 2007. Can J Vet Res 2015 Apr;79(2):155-9.
                    pubmed: 25852233
                  14. Tallmadge RL, Laverack M, Lejeune M, Crossley B, Diel DG. A multiplex real-time PCR assay for detection of equid herpesvirus 1 and 4. Sci Rep 2025 Oct 31;15(1):38201.
                    doi: 10.1038/s41598-025-22043-wpubmed: 41173927google scholar: lookup
                  15. Ewbank AC, Catão-Dias JL, Navas-Suarez PE, Duarte-Benvenuto A, Zamana-Ramblas R, Ferreira-Machado E, Lial HC, Ibáñez-Porras P, Sacristán I, Sacristán C. Novel Alpha-, Beta-, and Gammaherpesviruses in Neotropical Carnivores of Brazil. Transbound Emerg Dis 2024;2024:1347516.
                    doi: 10.1155/2024/1347516pubmed: 40303167google scholar: lookup
                  16. Haycock J, Maehr T, Dastjerdi A, Steinbach F. Asian elephant interferons alpha and beta and their anti-herpes viral activity. Front Immunol 2025;16:1533038.
                    doi: 10.3389/fimmu.2025.1533038pubmed: 40201174google scholar: lookup
                  17. Khan A, Olajide E, Friedrich M, Holt A, Goehring LS. Evaluation of Non-Invasive Sampling Techniques for the Molecular Surveillance of Equid Herpesviruses in Yearling Horses. Viruses 2024 Jul 7;16(7).
                    doi: 10.3390/v16071091pubmed: 39066254google scholar: lookup