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Equine veterinary journal2006; 38(3); 252-257; doi: 10.2746/042516406776866453

Quantification by real-time PCR of the magnitude and duration of leucocyte-associated viraemia in horses infected with neuropathogenic vs. non-neuropathogenic strains of EHV-1.

Abstract: Neurological disease in horses caused by infection with certain 'paralytic' strains of equine herpesvirus-1 (EHV-1) is a potentially devastating condition the pathogenesis of which is poorly understood. Preliminary observations in both experimentally induced and naturally occurring cases of the central nervous system disease have revealed a more robust cell-associated viraemia in horses infected with paralytic isolates of EHV-1, relative to horses infected with abortigenic isolates. To investigate further this pathogenesis-relevant question, the present study was performed using a greater number of horses and a more precise method for quantification of EHV-1 DNA present in viraemic leucocytes. Objective: To compare the magnitude and duration of leucocyte-associated viraemia in seronegative, age-matched foals following infection with paralytic vs. abortigenic isolates of EHV-1. Methods: Peripheral blood mononuclear cells (PBMC) were collected from 20 weanling foals at 2, 4, 7, 9, 11, 14 and 21 days after intranasal inoculation with either paralytic or abortigenic isolates of EHV-1. The amount of EHV-1 DNA present in each PBMC sample was measured by real-time quantitative PCR. Results: Foals inoculated with paralytic strains of EHV-1 developed both a greater magnitude and longer duration of PBMC-associated viraemia than foals inoculated with abortigenic strains of the virus. Conclusions: Both the higher magnitude and longer duration of cell-associated viraemia contribute to the risk for development of neurological signs in horses infected with paralytic strains of EHV-1. Conclusions: Our results provide empirically derived, scientific data that contributes to a better understanding of the pathogenetic basis for the differing abilities of paralytic and abortigenic strains of EHV-1 to cause post infection central nervous system disease in the horse. The findings identify the importance of minimising the quantitative burden of viraemic leucocytes that follows exposure to the virus, by the use of effective therapeutic antiviral drugs and efficacious prophylactic vaccines that stimulate cytotoxic immune responses against EHV-1 infected cells.
Publication Date: 2006-05-19 PubMed ID: 16706281DOI: 10.2746/042516406776866453Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates the differences in how paralytic and abortigenic strains of the equine herpesvirus-1 (EHV-1) affect horses, specifically by analyzing the intensity and length of viraemia in white blood cells, known as leucocytes.

Study Objective

The main purpose of this study was to unravel the discrepancies in the magnitude and duration of white blood cell (leucocyte)-linked viraemia in horses following exposure to either the paralytic or abortigenic forms of the EHV-1 virus. The researchers intended to extend their initial observations regarding the prevalence of a stronger cell-related viraemia in horses struck with paralytic forms, compared to those with abortigenic varieties of EHV-1.

Methods

  • The researchers deliberately exposed 20 young, seronegative foals to either paralytic or abortigenic forms of EHV-1 through intranasal inoculation.
  • The research team then collected peripheral blood mononuclear cells (PBMC) samples from these foals 2, 4, 7, 9, 11, 14, and 21 days after the inoculation.
  • Finally, the team utilized real-time quantitative PCR to measure the amount of EHV-1 DNA present in each PBMC sample.

Results

The findings suggested that foals exposed to paralytic EHV-1 strains developed a grander magnitude and longer duration of PBMC-associated viraemia compared to foals exposed to abortigenic strains of the virus.

Conclusions

The results pointed to the higher intensity and longer period of cell-related viraemia as factors that contribute to increasing the risk of neurological symptoms in horses infected with paralytic strains of EHV-1. The researchers concluded that their data provide significant insights into the varying ability of paralytic and abortigenic EHV-1 strains to cause post-infection central nervous system disease in horses. These results highlight the relevance of reducing the quantitative load of viraemic leucocytes following exposure to EHV-1, possibly through the application of effective antiviral drugs and prophylactic vaccines that trigger immune responses against EHV-1 infected cells.

Cite This Article

APA
Allen GP, Breathnach CC. (2006). Quantification by real-time PCR of the magnitude and duration of leucocyte-associated viraemia in horses infected with neuropathogenic vs. non-neuropathogenic strains of EHV-1. Equine Vet J, 38(3), 252-257. https://doi.org/10.2746/042516406776866453

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 38
Issue: 3
Pages: 252-257

Researcher Affiliations

Allen, G P
  • Maxwell H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky 40546-0099, USA.
Breathnach, C C

    MeSH Terms

    • Animals
    • DNA, Viral / analysis
    • Female
    • Herpesviridae Infections / diagnosis
    • Herpesviridae Infections / veterinary
    • Herpesviridae Infections / virology
    • Herpesvirus 1, Equid / isolation & purification
    • Herpesvirus 1, Equid / pathogenicity
    • Horse Diseases / diagnosis
    • Horse Diseases / virology
    • Horses
    • Leukocytes, Mononuclear / virology
    • Male
    • Polymerase Chain Reaction / methods
    • Polymerase Chain Reaction / veterinary
    • Viremia / diagnosis
    • Viremia / veterinary
    • Viremia / virology

    Citations

    This article has been cited 19 times.
    1. Black JB, Frampton AR. Anti-inflammatory compounds reduce equine herpesvirus type 1 replication and cell-to-cell spread.. Front Vet Sci 2023;10:1165917.
      doi: 10.3389/fvets.2023.1165917pubmed: 37275614google scholar: lookup
    2. 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
    3. 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
    4. 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
    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. 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
    7. 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
    8. Preziuso S, Sgorbini M, Marmorini P, Cuteri V. Equid alphaherpesvirus 1 from Italian Horses: Evaluation of the Variability of the ORF30, ORF33, ORF34 and ORF68 Genes.. Viruses 2019 Sep 13;11(9).
      doi: 10.3390/v11090851pubmed: 31540321google scholar: lookup
    9. Garvey M, Lyons R, Hector RD, Walsh C, Arkins S, Cullinane A. Molecular Characterisation of Equine Herpesvirus 1 Isolates from Cases of Abortion, Respiratory and Neurological Disease in Ireland between 1990 and 2017.. Pathogens 2019 Jan 15;8(1).
      doi: 10.3390/pathogens8010007pubmed: 30650561google scholar: lookup
    10. 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
    11. Bryant NA, Wilkie GS, Russell CA, Compston L, Grafham D, Clissold L, McLay K, Medcalf L, Newton R, Davison AJ, Elton DM. Genetic diversity of equine herpesvirus 1 isolated from neurological, abortigenic and respiratory disease outbreaks.. Transbound Emerg Dis 2018 Jun;65(3):817-832.
      doi: 10.1111/tbed.12809pubmed: 29423949google scholar: lookup
    12. Maxwell LK, Bentz BG, Gilliam LL, Ritchey JW, Pusterla N, Eberle R, Holbrook TC, McFarlane D, Rezabek GB, Meinkoth J, Whitfield C, Goad CL, Allen GP. Efficacy of the early administration of valacyclovir hydrochloride for the treatment of neuropathogenic equine herpesvirus type-1 infection in horses.. Am J Vet Res 2017 Oct;78(10):1126-1139.
      doi: 10.2460/ajvr.78.10.1126pubmed: 28945127google scholar: lookup
    13. Franz M, Goodman LB, Van de Walle GR, Osterrieder N, Greenwood AD. A Point Mutation in a Herpesvirus Co-Determines Neuropathogenicity and Viral Shedding.. Viruses 2017 Jan 10;9(1).
      doi: 10.3390/v9010006pubmed: 28075374google scholar: lookup
    14. Marenzoni ML, Bietta A, Lepri E, Casagrande Proietti P, Cordioli P, Canelli E, Stefanetti V, Coletti M, Timoney PJ, Passamonti F. Role of equine herpesviruses as co-infecting agents in cases of abortion, placental disease and neonatal foal mortality.. Vet Res Commun 2013 Dec;37(4):311-7.
      doi: 10.1007/s11259-013-9578-6pubmed: 24052369google scholar: lookup
    15. Hora AS, Tonietti PO, Guerra JM, Leme MC, Pena HF, Maiorka PC, Brandão PE. Felid herpesvirus 1 as a causative agent of severe nonsuppurative meningoencephalitis in a domestic cat.. J Clin Microbiol 2013 Feb;51(2):676-9.
      doi: 10.1128/JCM.02462-12pubmed: 23152556google scholar: lookup
    16. Smith KL, Li Y, Breheny P, Cook RF, Henney PJ, Sells S, Pronost S, Lu Z, Crossley BM, Timoney PJ, Balasuriya UB. New real-time PCR assay using allelic discrimination for detection and differentiation of equine herpesvirus-1 strains with A2254 and G2254 polymorphisms.. J Clin Microbiol 2012 Jun;50(6):1981-8.
      doi: 10.1128/JCM.00135-12pubmed: 22493339google scholar: lookup
    17. Azab W, Osterrieder N. Glycoproteins D of equine herpesvirus type 1 (EHV-1) and EHV-4 determine cellular tropism independently of integrins.. J Virol 2012 Feb;86(4):2031-44.
      doi: 10.1128/JVI.06555-11pubmed: 22171258google scholar: lookup
    18. 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.
    19. Goodman LB, Loregian A, Perkins GA, Nugent J, Buckles EL, Mercorelli B, Kydd JH, Palù G, Smith KC, Osterrieder N, Davis-Poynter N. A point mutation in a herpesvirus polymerase determines neuropathogenicity.. PLoS Pathog 2007 Nov;3(11):e160.
      doi: 10.1371/journal.ppat.0030160pubmed: 17997600google scholar: lookup