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The Journal of general virology1994; 75 ( Pt 8); 2007-2016; doi: 10.1099/0022-1317-75-8-2007

The trigeminal ganglion is a location for equine herpesvirus 1 latency and reactivation in the horse.

Abstract: Four specific pathogen-free ponies were infected intranasally with equine herpesvirus 1 (EHV-1) and two were similarly infected with an EHV-1 thymidine kinase deletion mutant. The primary infections were characterized by a transient fever accompanied by virus shedding into nasal mucus and viraemia. No virus was detected in clinical specimens after 15 days post-infection. Two months later a reactivation stimulus was administered to all six ponies and only the four that had been previously inoculated with wild-type EHV-1 shed virus into nasal mucus (for 10 days), proving the presence of a latent infection. No recurrence of viraemia was observed. The animals were monitored for a further 6 weeks and were consistently shown to be free from infectious virus. Tissues were then obtained postmortem. Co-cultivation of explanted trigeminal ganglia from two out of the four ponies that carried the wild-type virus yielded cultures positive for infectious virus. Apart from nasal epithelium, no infectious virus was recovered from any other tissue. PCR confirmed the presence of virus DNA in the ganglia from all six ponies. Lymphoid tissues also yielded positive signals using this technique. The relevance of virus detection by PCR in lymphoid and neural tissues is discussed in relation to the potential for reactivation of latent virus in the host. However, evidence is presented to show that EHV-1 is neurotropic and, in common with other members of the alpha-herpesvirus subfamily, establishes latency in sensory ganglia from which virus can be reactivated.
Publication Date: 1994-08-01 PubMed ID: 8046404DOI: 10.1099/0022-1317-75-8-2007Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research study explores how the equine herpesvirus 1 (EHV-1) exists in a latent form in the trigeminal ganglion of horses, can get reactivated, and its possible health impact.

About the Study

  • In this experiment, four pathogen-free ponies were selected for intranasal infection with equine herpesvirus 1 (EHV-1), and two were infected with an EHV-1 thymidine kinase deletion mutant.
  • The primary infections led to a transient fever, virus shedding into nasal mucus, and viraemia (presence of viruses in the blood). After 15 days post-infection, no virus was detected in clinical specimens.

Reactivation of the Virus

  • Two months after the primary infection, a reactivation stimulus was given to the ponies, following which the four ponies previously infected with wild-type EHV-1 began to shed the virus into nasal mucus, indicating the presence of a latent infection. Recurrence of viraemia wasn’t observed.
  • Even after monitoring the animals for another six weeks, they were found to be free from the infectious virus.
  • On carrying out a postmortem examination, co-cultivation of explanted trigeminal ganglia from two out of the four ponies infected with wild-type virus resulted in cultures testing positive for the virus. But apart from nasal epithelium, the infectious virus couldn’t be recovered from any other tissue.

PCR Virus Detection

  • Using a PCR test, viral DNA was detected in the ganglia from all six ponies. Even lymphoid tissues showed positive results.
  • The study discusses the relevance of virus detection by PCR in lymphoid and neural tissues in relation to the potential for reactivation of the latent virus in the host.
  • This draws the conclusion that EHV-1 behaves similarly to other members of the alpha-herpesvirus subfamily in being neurotropic (having an affinity for neural tissues) and it establishes latency in sensory ganglia, from where it can be reactivated.

Cite This Article

APA
Slater JD, Borchers K, Thackray AM, Field HJ. (1994). The trigeminal ganglion is a location for equine herpesvirus 1 latency and reactivation in the horse. J Gen Virol, 75 ( Pt 8), 2007-2016. https://doi.org/10.1099/0022-1317-75-8-2007

Publication

ISSN: 0022-1317
NlmUniqueID: 0077340
Country: England
Language: English
Volume: 75 ( Pt 8)
Pages: 2007-2016

Researcher Affiliations

Slater, J D
  • Department of Veterinary Medicine, University of Cambridge, U.K.
Borchers, K
    Thackray, A M
      Field, H J

        MeSH Terms

        • Administration, Intranasal
        • Animals
        • Herpesviridae Infections / microbiology
        • Herpesviridae Infections / veterinary
        • Herpesvirus 1, Equid / genetics
        • Herpesvirus 1, Equid / growth & development
        • Horse Diseases / microbiology
        • Horses
        • Nucleic Acid Hybridization
        • Polymerase Chain Reaction
        • Specific Pathogen-Free Organisms
        • Thymidine Kinase / genetics
        • Tissue Distribution
        • Trigeminal Ganglion / microbiology
        • Viremia
        • Virus Activation
        • Virus Cultivation
        • Virus Latency

        Citations

        This article has been cited 35 times.
        1. Van Crombrugge E, Vanbeylen E, Van Cleemput J, Van den Broeck W, Laval K, Nauwynck H. Bacterial Toxins from Staphylococcus aureus and Bordetella bronchiseptica Predispose the Horse's Respiratory Tract to Equine Herpesvirus Type 1 Infection.. Viruses 2022 Jan 14;14(1).
          doi: 10.3390/v14010149pubmed: 35062352google scholar: lookup
        2. 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
        3. El-Hage C, Mekuria Z, Dynon K, Hartley C, McBride K, Gilkerson J. Association of Equine Herpesvirus 5 with Mild Respiratory Disease in a Survey of EHV1, -2, -4 and -5 in 407 Australian Horses.. Animals (Basel) 2021 Nov 30;11(12).
          doi: 10.3390/ani11123418pubmed: 34944194google scholar: lookup
        4. Samoilowa S, Giessler KS, Torres CEM, Hussey GS, Allum A, Fux R, Jerke C, Kiupel M, Matiasek K, Sledge DG, Goehring LS. Equid herpesvirus-1 Distribution in Equine Lymphoid and Neural Tissues 70 Days Post Infection.. Pathogens 2021 Jun 5;10(6).
          doi: 10.3390/pathogens10060707pubmed: 34198884google scholar: lookup
        5. Zarski LM, Vaala WE, Barnett DC, Bain FT, Soboll Hussey G. A Live-Attenuated Equine Influenza Vaccine Stimulates Innate Immunity in Equine Respiratory Epithelial Cell Cultures That Could Provide Protection From Equine Herpesvirus 1.. Front Vet Sci 2021;8:674850.
          doi: 10.3389/fvets.2021.674850pubmed: 34179166google scholar: lookup
        6. Laval K, Poelaert KCK, Van Cleemput J, Zhao J, Vandekerckhove AP, Gryspeerdt AC, Garré B, van der Meulen K, Baghi HB, Dubale HN, Zarak I, Van Crombrugge E, Nauwynck HJ. The Pathogenesis and Immune Evasive Mechanisms of Equine Herpesvirus Type 1.. Front Microbiol 2021;12:662686.
          doi: 10.3389/fmicb.2021.662686pubmed: 33746936google scholar: lookup
        7. Zarski LM, Giessler KS, Jacob SI, Weber PSD, McCauley AG, Lee Y, Soboll Hussey G. Identification of Host Factors Associated with the Development of Equine Herpesvirus Myeloencephalopathy by Transcriptomic Analysis of Peripheral Blood Mononuclear Cells from Horses.. Viruses 2021 Feb 24;13(3).
          doi: 10.3390/v13030356pubmed: 33668216google scholar: lookup
        8. Zarski LM, Weber PSD, Lee Y, Soboll Hussey G. Transcriptomic Profiling of Equine and Viral Genes in Peripheral Blood Mononuclear Cells in Horses during Equine Herpesvirus 1 Infection.. Pathogens 2021 Jan 7;10(1).
          doi: 10.3390/pathogens10010043pubmed: 33430330google scholar: lookup
        9. Giessler KS, Samoilowa S, Soboll Hussey G, Kiupel M, Matiasek K, Sledge DG, Liesche F, Schlegel J, Fux R, Goehring LS. Viral Load and Cell Tropism During Early Latent Equid Herpesvirus 1 Infection Differ Over Time in Lymphoid and Neural Tissue Samples From Experimentally Infected Horses.. Front Vet Sci 2020;7:621.
          doi: 10.3389/fvets.2020.00621pubmed: 33102556google scholar: lookup
        10. 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
        11. Stasiak K, Dunowska M, Rola J. Outbreak of equid herpesvirus 1 abortions at the Arabian stud in Poland.. BMC Vet Res 2020 Oct 6;16(1):374.
          doi: 10.1186/s12917-020-02586-ypubmed: 33023592google scholar: lookup
        12. Lecollinet S, Pronost S, Coulpier M, Beck C, Gonzalez G, Leblond A, Tritz P. Viral Equine Encephalitis, a Growing Threat to the Horse Population in Europe?. Viruses 2019 Dec 24;12(1).
          doi: 10.3390/v12010023pubmed: 31878129google scholar: lookup
        13. Oladunni FS, Horohov DW, Chambers TM. EHV-1: A Constant Threat to the Horse Industry.. Front Microbiol 2019;10:2668.
          doi: 10.3389/fmicb.2019.02668pubmed: 31849857google scholar: lookup
        14. Faisal M, Purbayu M, Shavalier MA, Marsh TL, Loch TP. Shedding of the Salmonid Herpesvirus-3 by Infected Lake Trout (Salvelinus namaycush).. Viruses 2019 Jun 26;11(7).
          doi: 10.3390/v11070580pubmed: 31247927google scholar: lookup
        15. Brown LJ, Brown G, Kydd J, Stout TAE, Schulman ML. Failure to detect equid herpesvirus types 1 and 4 DNA in placentae and healthy new-born Thoroughbred foals.. J S Afr Vet Assoc 2019 May 30;90(0):e1-e5.
          doi: 10.4102/jsava.v90i0.1736pubmed: 31170779google scholar: lookup
        16. Holz CL, Sledge DG, Kiupel M, Nelli RK, Goehring LS, Soboll Hussey G. Histopathologic Findings Following Experimental Equine Herpesvirus 1 Infection of Horses.. Front Vet Sci 2019;6:59.
          doi: 10.3389/fvets.2019.00059pubmed: 30886853google scholar: lookup
        17. Poelaert KCK, Van Cleemput J, Laval K, Favoreel HW, Couck L, Van den Broeck W, Azab W, Nauwynck HJ. Equine Herpesvirus 1 Bridles T Lymphocytes To Reach Its Target Organs.. J Virol 2019 Apr 1;93(7).
          doi: 10.1128/JVI.02098-18pubmed: 30651370google scholar: lookup
        18. Matczuk AK, Skarbek M, Jackulak NA, Bażanów BA. Molecular characterisation of equid alphaherpesvirus 1 strains isolated from aborted fetuses in Poland.. Virol J 2018 Dec 3;15(1):186.
          doi: 10.1186/s12985-018-1093-5pubmed: 30509297google scholar: lookup
        19. Wimer CL, Schnabel CL, Perkins G, Babasyan S, Freer H, Stout AE, Rollins A, Osterrieder N, Goodman LB, Glaser A, Wagner B. The deletion of the ORF1 and ORF71 genes reduces virulence of the neuropathogenic EHV-1 strain Ab4 without compromising host immunity in horses.. PLoS One 2018;13(11):e0206679.
          doi: 10.1371/journal.pone.0206679pubmed: 30440016google scholar: lookup
        20. Muscat KE, Padalino B, Hartley CA, Ficorilli N, Celi P, Knight P, Raidal S, Gilkerson JR, Muscatello G. Equine Transport and Changes in Equid Herpesvirus' Status.. Front Vet Sci 2018;5:224.
          doi: 10.3389/fvets.2018.00224pubmed: 30320126google scholar: lookup
        21. Poelaert KCK, Van Cleemput J, Laval K, Favoreel HW, Soboll Hussey G, Maes RK, Nauwynck HJ. Abortigenic but Not Neurotropic Equine Herpes Virus 1 Modulates the Interferon Antiviral Defense.. Front Cell Infect Microbiol 2018;8:312.
          doi: 10.3389/fcimb.2018.00312pubmed: 30258819google scholar: lookup
        22. Schnabel CL, Wimer CL, Perkins G, Babasyan S, Freer H, Watts C, Rollins A, Osterrieder N, Wagner B. Deletion of the ORF2 gene of the neuropathogenic equine herpesvirus type 1 strain Ab4 reduces virulence while maintaining strong immunogenicity.. BMC Vet Res 2018 Aug 22;14(1):245.
          doi: 10.1186/s12917-018-1563-4pubmed: 30134896google scholar: lookup
        23. Van Cleemput J, Poelaert KCK, Laval K, Maes R, Hussey GS, Van den Broeck W, Nauwynck HJ. Access to a main alphaherpesvirus receptor, located basolaterally in the respiratory epithelium, is masked by intercellular junctions.. Sci Rep 2017 Nov 30;7(1):16656.
          doi: 10.1038/s41598-017-16804-5pubmed: 29192251google scholar: lookup
        24. Hue ES, Richard EA, Fortier CI, Fortier GD, Paillot R, Raue R, Pronost SL. Equine PBMC Cytokines Profile after In Vitro α- and γ-EHV Infection: Efficacy of a Parapoxvirus Ovis Based-Immunomodulator Treatment.. Vaccines (Basel) 2017 Sep 19;5(3).
          doi: 10.3390/vaccines5030028pubmed: 28925977google scholar: lookup
        25. Cymerys J, Słońska A, Tucholska A, Golke A, Chmielewska A, Bańbura MW. Influence of long-term equine herpesvirus type 1 (EHV-1) infection on primary murine neurons-the possible effects of the multiple passages of EHV-1 on its neurovirulence.. Folia Microbiol (Praha) 2018 Jan;63(1):1-11.
          doi: 10.1007/s12223-017-0528-5pubmed: 28409422google scholar: lookup
        26. Wagner B, Perkins G, Babasyan S, Freer H, Keggan A, Goodman LB, Glaser A, Torsteinsdóttir S, Svansson V, Björnsdóttir S. Neonatal Immunization with a Single IL-4/Antigen Dose Induces Increased Antibody Responses after Challenge Infection with Equine Herpesvirus Type 1 (EHV-1) at Weanling Age.. PLoS One 2017;12(1):e0169072.
          doi: 10.1371/journal.pone.0169072pubmed: 28045974google scholar: lookup
        27. Negussie H, Li Y, Tessema TS, Nauwynck HJ. Replication characteristics of equine herpesvirus 1 and equine herpesvirus 3: comparative analysis using ex vivo tissue cultures.. Vet Res 2016 Jan 15;47:19.
          doi: 10.1186/s13567-016-0305-5pubmed: 26768993google scholar: lookup
        28. Słońska A, Cymerys J, Godlewski MM, Dzieciątkowski T, Tucholska A, Chmielewska A, Golke A, Bańbura MW. Equine herpesvirus type 1 (EHV-1)-induced rearrangements of actin filaments in productively infected primary murine neurons.. Arch Virol 2014 Jun;159(6):1341-9.
          doi: 10.1007/s00705-013-1949-3pubmed: 24352436google scholar: lookup
        29. Brosnahan MM, Damiani A, van de Walle G, Erb H, Perkins GA, Osterrieder N. The effect of siRNA treatment on experimental equine herpesvirus type 1 (EHV-1) infection in horses.. Virus Res 2010 Feb;147(2):176-81.
        30. Olsen TF. Equine herpesvirus myeloencephalopathy in a 14-year-old quarter horse stallion.. Can Vet J 2001 Mar;42(3):217-20.
          pubmed: 11265193
        31. Bartels T, Steinbach F, Hahn G, Ludwig H, Borchers K. In situ study on the pathogenesis and immune reaction of equine herpesvirus type 1 (EHV-1) infections in mice.. Immunology 1998 Mar;93(3):329-34.
        32. Feng X, Thompson YG, Lewis JB, Caughman GB. Expression and function of the equine herpesvirus 1 virion-associated host shutoff homolog.. J Virol 1996 Dec;70(12):8710-8.
        33. Tanaka S, Imamura T, Sakaguchi M, Mannen K, Matsuo K. Acetylcholine activates latent pseudorabies virus in pigs.. Arch Virol 1996;141(1):161-6.
          doi: 10.1007/BF01718597pubmed: 8629944google scholar: lookup
        34. Pfeffer M, Wiedmann M, Batt CA. Applications of DNA amplification techniques in veterinary diagnostics.. Vet Res Commun 1995;19(5):375-407.
          doi: 10.1007/BF01839319pubmed: 8560754google scholar: lookup
        35. Crabb BS, MacPherson CM, Reubel GH, Browning GF, Studdert MJ, Drummer HE. A type-specific serological test to distinguish antibodies to equine herpesviruses 4 and 1.. Arch Virol 1995;140(2):245-58.
          doi: 10.1007/BF01309860pubmed: 7710353google scholar: lookup