Analyze Diet
Journal of veterinary internal medicine2023; 38(3); 1765-1791; doi: 10.1111/jvim.16958

Viremia and nasal shedding for the diagnosis of equine herpesvirus-1 infection in domesticated horses.

Abstract: Equine herpesvirus type 1 (EHV-1) infection is associated with upper respiratory disease, EHM, abortions, and neonatal death. Objective: Are nasal secretions a more sensitive biological sample compared to blood for the detection of EHV-1 infection? How long is EHV-1 detectable after primary infection by PCR? Methods: MedLine and Web of Science searches identified original peer-reviewed reports evaluating nasal shedding and viremia using virus isolation methods or PCR published in English before October 9, 2023. Results: Sixty experimental and 20 observational studies met inclusion criteria. EHV-1 detection frequency by qPCR in nasal secretions and blood from naturally-infected horses with fever and respiratory signs were 15% and 9%, respectively; qPCR detection rates in nasal secretions and blood from horses with suspected EHM were 94% and 70%, respectively. In experimental studies the sensitivity of qPCR matched or exceeded that seen for virus isolation from either nasal secretions or blood. Detection of nasal shedding typically occurred within 2 days after EHV-1 inoculation with a detection period of 3 to 7 days. Viremia lasted 2 to 7 days and was usually detected ≥1 days after positive identification of EHV-1 in nasal secretions. Nasal shedding and viremia decreased over time and remained detectable in some horses for several weeks after inoculation. Conclusions: Under experimental conditions, blood and nasal secretions have similar sensitivity for the detection of EHV-1 when horses are sampled on multiple consecutive days. In contrast, in observational studies detection of EHV-1 in nasal secretions was consistently more successful.
Publication Date: 2023-12-09 PubMed ID: 38069548PubMed Central: PMC11099742DOI: 10.1111/jvim.16958Google 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
  • Review

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 investigates the effectiveness of using nasal secretions versus blood samples in detecting Equine Herpesvirus Type 1 (EHV-1) in horses. The study uncovers that nasal secretions are generally more successful in identifying the virus compared to blood samples, especially under observational conditions.

Research Approach

  • The researchers conducted a comprehensive review of previously published original peer-reviewed studies on the topic. They used the MedLine and Web of Science databases to source these studies which discuss evaluating nasal shedding and viremia of EHV-1 under different conditions using varied methods like virus isolation and PCR.
  • These studies were done in English and were published before October 9, 2023.

Findings

  • The results came from sixty experimental studies and 20 observational studies. In testing for EHV-1 in naturally-infected horses showing symptoms of fever and respiratory issues, the detection rate of EHV-1 using quantitative PCR (qPCR) was higher in nasal secretions (15%) compared to blood samples (9%).
  • For horses with suspected equine herpes myeloencephalopathy (EHM), the percentages rose to 94% detection in nasal secretions and 70% in blood.
  • In experimental conditions, the sensitivity of qPCR either matched or exceeded the sensitivity seen in virus isolation from both nasal secretions and blood.
  • Nasal shedding was typically detectable within 2 days after EHV-1 inoculation and lasted for about 3-7 days.
  • Viremia took longer, usually detectable at least a day after positive identification in the nasal secretions and lasted between 2-7 days.
  • Both nasal shedding and viremia decreased over time but remained detectable in some cases for weeks post-inoculation.

Conclusions

  • Under controlled experimental conditions, blood and nasal secretion samples showed similar sensitivity in EHV-1 detection when sampled on multiple consecutive days.
  • In contrast, under observational study conditions, the detection of EHV-1 using nasal secretions as a sample was consistently more successful indicating that it may be a more viable and sensitive biological sample for EHV-1 detection in real-world settings.

Cite This Article

APA
Pusterla N, Dorman DC, Burgess BA, Goehring L, Gross M, Osterrieder K, Soboll Hussey G, Lunn DP. (2023). Viremia and nasal shedding for the diagnosis of equine herpesvirus-1 infection in domesticated horses. J Vet Intern Med, 38(3), 1765-1791. https://doi.org/10.1111/jvim.16958

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 38
Issue: 3
Pages: 1765-1791

Researcher Affiliations

Pusterla, Nicola
  • School of Veterinary Medicine, University of California, Davis, California, USA.
Dorman, David C
  • College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.
Burgess, Brandy A
  • College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Goehring, Lutz
  • College of Agriculture, Food and Environment, Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington, Kentucky, USA.
Gross, Margaret
  • College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.
Osterrieder, Klaus
  • Institut für Virologie, Freie Universität Berlin, Berlin, Germany.
Soboll Hussey, Gisela
  • College of Veterinary Medicine, Michigan State University, Veterinary Medical Center, East Lansing, Michigan, USA.
Lunn, David P
  • School of Veterinary Science, University of Liverpool, Leahurst Campus, Neston, UK.

MeSH Terms

  • Animals
  • Horses
  • Herpesvirus 1, Equid / isolation & purification
  • Viremia / veterinary
  • Viremia / diagnosis
  • Viremia / virology
  • Horse Diseases / virology
  • Horse Diseases / diagnosis
  • Herpesviridae Infections / veterinary
  • Herpesviridae Infections / diagnosis
  • Herpesviridae Infections / virology
  • Virus Shedding
  • Nose / virology
  • Real-Time Polymerase Chain Reaction / veterinary

Conflict of Interest Statement

Authors declare no conflict of interest.

References

This article includes 85 references
  1. Slater J. Equine herpesviruses. .
  2. Tewari SC, Prasad S. Comparative diagnostic value of the gel diffusion test and virus isolation in cell culture for detecting equine herpesvirus type 1 (EHV‐1). Rev Sci Tech 1983;2:1067‐1074.
    pubmed: 32993212
  3. Pusterla N, Madigan JE, Leutenegger CM. Real‐time polymerase chain reaction: a novel molecular diagnostic tool for equine infectious diseases. J Vet Intern Med 2006;20:3‐12.
    pubmed: 16496917
  4. Ataseven VS, Dağalp SB, Güzel M, Başaran Z, Tan MT, Geraghty B. Prevalence of equine herpesvirus‐1 and equine herpesvirus‐4 infections in equidae species in Turkey as determined by ELISA and multiplex nested PCR. Res Vet Sci 2009;86:339‐344.
    pubmed: 18649902
  5. Brown JA, Mapes S, Ball BA, Hodder ADJ, Liu IKM, Pusterla N. Prevalence of equine herpesvirus‐1 infection among thoroughbreds residing on a farm on which the virus was endemic. J Am Vet Med Assoc 2007;231:577‐580.
    pubmed: 17696859
  6. Damiani AM, de Vries M, Reimers G, Winkler S, Osterrieder N. A severe equine herpesvirus type 1 (EHV‐1) abortion outbreak caused by a neuropathogenic strain at a breeding farm in northern Germany. Vet Microbiol 2014;172:555‐562.
    pubmed: 25042527
  7. Estell KE, Dawson DR, Magdesian KG. Quantitative molecular viral loads in 7 horses with naturally occurring equine herpesvirus‐1 infection. Equine Vet J 2015;47:689‐693.
    pubmed: 25212737
  8. Marenzoni ML, Passamonti F, Cappelli K. Clinical, serological and molecular investigations of EHV‐1 and EHV‐4 in 15 unweaned thoroughbred foals. Vet Rec 2008;162:337‐341.
    pubmed: 18344498
  9. McFadden AM, Hanlon D, McKenzie RK. The first reported outbreak of equine herpesvirus myeloencephalopathy in New Zealand. N Z Vet J 2016;64:125‐134.
    pubmed: 26414406
  10. Ohta M, Nemoto M, Tsujimura K. Evaluation of the usefulness of a PCR assay performed at a clinical laboratory for the diagnosis of respiratory disease induced by equine herpesvirus type 1 in the field. J Equine Sci 2011;22:53‐56.
    pmc: PMC4013993pubmed: 24833987
  11. Pronost S, Legrand L, Pitel PH. Outbreak of equine herpesvirus myeloencephalopathy in France: a clinical and molecular investigation. Transbound Emerg Dis 2012;59:256‐263.
    pubmed: 21975071
  12. Pusterla N, Mapes S, Wilson WD. Diagnostic sensitivity of nasopharyngeal and nasal swabs for the molecular detection of EHV‐1. Vet Rec 2008;162:520‐521.
    pubmed: 18424850
  13. Pusterla N, Mapes S, Wilson WD. Use of viral loads in blood and nasopharyngeal secretions for the diagnosis of EHV‐1 infection in field cases. Vet Rec 2008;162:728‐729.
    pubmed: 18515763
  14. Pusterla N, Mapes S, Madigan JE. Prevalence of EHV‐1 in adult horses transported over long distances. Vet Rec 2009;165:473‐475.
    pubmed: 19850855
  15. Pusterla N, Wilson WD, Mapes S. Characterization of viral loads, strain and state of equine herpesvirus‐1 using real‐time PCR in horses following natural exposure at a racetrack in California. Vet J 2009;179:230‐239.
    pubmed: 18024200
  16. Pusterla N, Kass PH, Mapes S. Surveillance programme for important equine infectious respiratory pathogens in the USA. Vet Rec 2011;169:12.
    pubmed: 21676986
  17. Pusterla N, Mapes S, Akana N. Prevalence factors associated with equine herpesvirus type 1 infection in equids with upper respiratory tract infection and/or acute onset of neurological signs from 2008 to 2014. Vet Rec 2016;178:70.
    pubmed: 26607427
  18. Pusterla N, Barnum S, Miller J. Investigation of an EHV‐1 outbreak in the United States caused by a new H752 genotype. Pathogens 2021;10:747.
    pmc: PMC8231618pubmed: 34199153
  19. Pusterla N, James K, Barnum S, Delwart E. Investigation of three newly identified equine parvoviruses in blood and nasal fluid samples of clinically healthy horses and horses with acute onset of respiratory disease. Animals (Basel) 2021;11:3006.
    pmc: PMC8532786pubmed: 34680025
  20. Studdert MJ, Hartley CA, Dynon K. Outbreak of equine herpesvirus type 1 myeloencephalitis: new insights from virus identification by PCR and the application of an EHV‐1‐specific antibody detection ELISA. Vet Rec 2003;153:417‐423.
    pubmed: 14582730
  21. Sutton G, Garvey M, Cullinane A. 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;11:916.
    pmc: PMC6832873pubmed: 31590336
  22. Walter J, Seeh C, Fey K, Bleul U, Osterrieder N. Clinical observations and management of a severe equine herpesvirus type 1 outbreak with abortion and encephalomyelitis. Acta Vet Scand 2013;55:19.
    pmc: PMC3630004pubmed: 23497661
  23. Wang L, Raidal SL, Pizzirani A, Wilcox GE. Detection of respiratory herpesviruses in foals and adult horses determined by nested multiplex PCR. Vet Microbiol 2007;121:18‐28.
    pubmed: 17208393
  24. Bannai H, Nemoto M, Tsujimura K. Comparison of protective efficacies between intranasal and intramuscular vaccination of horses with a modified live equine herpesvirus type‐1 vaccine. Vet Microbiol 2018;222:18‐24.
    pubmed: 30080668
  25. Bannai H, Kambayashi Y, Nemoto M, Ohta M, Tsujimura K. Experimental challenge of horses after prime‐boost immunization with a modified live equid alphaherpesvirus 1 vaccine administered by two different routes. Arch Virol 2023;168:27.
    pubmed: 36596958
  26. Breathnach CC, Yeargan MR, Sheoran AS. The mucosal humoral immune response of the horse to infective challenge and vaccination with equine herpesvirus‐1 antigens. Equine Vet J 2001;33:651‐657.
    pubmed: 11770985
  27. Breathnach CC, Yeargan MR, Timoney JF, Allen GP. Detection of equine herpesvirus‐specific effector and memory cytotoxic immunity in the equine upper respiratory tract. Vet Immunol Immunopathol 2006;111:117‐125.
    pubmed: 16472871
  28. Bridges CG, Edington N. Genetic restriction of cytolysis during equid herpesvirus 1 subtype 2 infection. Clin Exp Immunol 1987;70:276‐282.
    pmc: PMC1542070pubmed: 2827921
  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;147:176‐181.
    pmc: PMC7114471pubmed: 19896512
  30. Burki F, Rossmanith W, Nowotny N. Viremia and abortions are not prevented by 2 commercial equine herpesvirus‐1 vaccines after experimental challenge of horses. Vet Quart 1990;12:80‐86.
    pubmed: 2163560
  31. Burrows R, Goodridge D, Denyer MS. Trials of an inactivated equid herpesvirus 1 vaccine: challenge with a subtype 1 virus. Vet Rec 1984;114:369‐374.
    pubmed: 6328728
  32. Cornick J, Martens J, Martens R, Crandell R, McConnell S, Kit S. Safety and efficacy of a thymidine kinase negative equine herpesvirus‐1 vaccine in young horses. Can J Vet Res 1990;54:260‐266.
    pmc: PMC1255647pubmed: 2162730
  33. Dolby CA, Hannant D, Mumford JA. Response of ponies to adjuvanted EHV‐1 whole virus vaccine and challenge with virus of the homologous strain. Br Vet J 1995;151:27‐37.
    pubmed: 7735868
  34. Edington N, Bridges CG. One way protection between equid herpesvirus 1 and 4 in vivo. Res Vet Sci 1990;48:235‐239.
    pubmed: 2159176
  35. Edington N, Smyth B, Griffiths L. The role of endothelial cell infection in the endometrium, placenta and foetus of equid herpesvirus 1 (EHV‐1) abortions. J Comp Pathol 1991;104:379‐387.
    pubmed: 1651960
  36. Foote CE, Raidal SL, Pecenpetelovska G, Wellington JE, Whalley JM. Inoculation of mares and very young foals with EHV‐1 glycoproteins D and B reduces virus shedding following respiratory challenge with EHV‐1. Vet Immunol Immunopathol 2006;111:97‐108.
    pubmed: 16504306
  37. Gardiner DW, Lunn DP, Goehring LS. Strain impact on equine herpesvirus type 1 (EHV‐1) abortion models: viral loads in fetal and placental tissues and foals. Vaccine 2012;30:6564‐6572.
    pubmed: 22944628
  38. Garré B, Gryspeerdt A, Croubels S, de Backer P, Nauwynck H. Evaluation of orally administered valacyclovir in experimentally EHV1‐infected ponies. Vet Microbiol 2009;135:214‐221.
    pubmed: 18986780
  39. Gibson JS, Slater JD, Awan AR, Field HJ. Pathogenesis of equine herpesvirus‐1 in specific pathogen‐free foals: primary and secondary infections and reactivation. Arch Virol 1992;123:351‐366.
    pubmed: 1314051
  40. Gibson JS, Slater JD, Field HJ. The pathogenicity of Ab4p, the sequenced strain of equine herpesvirus‐1, in specific pathogen‐free foals. Virology 1992;189:317‐319.
    pubmed: 1318607
  41. Gibson JS, O'Neill T, Thackray A, Hannant D, Field HJ. Serological responses of specific pathogen‐free foals to equine herpesvirus‐1: primary and secondary infection, and reactivation. Vet Microbiol 1992;32:199‐214.
    pubmed: 1333670
  42. Gibson JS, Slater JD, Field HJ. The activity of (S)‐1‐[(3‐hydroxy‐2‐phosphonyl methoxy) propyl] cytosine (HPMPC) against equine herpesvirus‐1 (EHV‐1) in cell cultures, mice and horses. Antiviral Res 1992;19:219‐232.
    pubmed: 1332605
  43. Gleeson LJ, Coggins L. Response of pregnant mares to equine herpesvirus 1 (EHV1). Cornell Vet 1980;70:391‐400.
    pubmed: 6257449
  44. Goehring LS, van Maanen C, Berendsen M. Experimental infection with neuropathogenic equid herpesvirus type 1 (EHV‐1) in adult horses. Vet J 2010;186:180‐187.
    pubmed: 19726209
  45. Goehring LS, Wagner B, Bigbie R. Control of EHV‐1 viremia and nasal shedding by commercial vaccines. Vaccine 2010;28:5203‐5211.
    pubmed: 20538091
  46. Goodman LB, Loregian A, Perkins GA. A point mutation in a herpesvirus polymerase determines neuropathogenicity. PLoS Pathog 2007;3:e160.
    pmc: PMC2065875pubmed: 17997600
  47. Gryspeerdt AC, Vandekerckhove AP, Garre B. Differences in replication kinetics and cell tropism between neurovirulent and non‐neurovirulent EHV1 strains during the acute phase of infection in horses. Vet Microbiol 2010;142:242‐253.
    pubmed: 19926232
  48. Gupta AK, Rattan B, Malik P. Experimental infection of donkeys with EHV‐1 of horse origin—a study. J Equine Sci 2000;11:29‐33.
  49. Hannant D, Jessett DM, O'Neill T, Dolby CA, Cook RF, Mumford JA. Responses of ponies to equid herpesvirus‐1 ISCOM vaccination and challenge with virus of the homologous strain. Res Vet Sci 1993;54:299‐305.
    pubmed: 8393207
  50. Heldens JG, Hannant D, Cullinane AA. Clinical and virological evaluation of the efficacy of an inactivated EHV1 and EHV4 whole virus vaccine (Duvaxyn EHV1,4). Vaccination/challenge experiments in foals and pregnant mares. Vaccine 2001;19:4307‐4317.
    pubmed: 11457558
  51. Holz CL, Nelli RK, Wilson ME. Viral genes and cellular markers associated with neurological complications during herpesvirus infections. J Gen Virol 2017;98:1439‐1454.
    pubmed: 28631601
  52. Hussey SB, Clark R, Lunn KF. Detection and quantification of equine herpesvirus‐1 viremia and nasal shedding by real‐time polymerase chain reaction. J Vet Diagn Invest 2006;18:335‐342.
    pubmed: 16921871
  53. Hussey GS, Goehring LS, Lunn DP. Experimental infection with equine herpesvirus type 1 (EHV‐1) induces chorioretinal lesions. Vet Res 2013;44:118.
    pmc: PMC4028784pubmed: 24308772
  54. Kydd JH, Wattrang E, Hannant D. Pre‐infection frequencies of equine herpesvirus‐1 specific, cytotoxic T lymphocytes correlate with protection against abortion following experimental infection of pregnant mares. Vet Immunol Immunopathol 2003;96:207‐217.
    pubmed: 14592733
  55. Kydd JH, Hannant D, Robinson RS, Bryant N, Osterrieder N. Vaccination of foals with a modified live, equid herpesvirus‐1 gM deletion mutant (RacHΔgM) confers partial protection against infection. Vaccine 2020;38:388‐398.
    pubmed: 31629571
  56. Martens JG, Martens RJ, Crandell RA. Molecular confirmation of an abortigenic strain of equine herpesvirus 1 (subtype 1) in a pregnant mare study. Cornell Vet 1989;79:363‐371.
    pubmed: 2548809
  57. Maxwell LK, Bentz BG, Gilliam LL. 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;78:1126‐1139.
    pmc: PMC6440545pubmed: 28945127
  58. Minke JM, Fischer L, Baudu P. Use of DNA and recombinant canarypox viral (ALVAC) vectors for equine herpes virus vaccination. Vet Immunol Immunopathol 2006;111:47‐57.
    pubmed: 16580075
  59. Mohd‐Azmi ML, Gibson J, Rixon F. Protection of specific‐pathogen‐free (Spf) foals from severe equine herpesvirus type‐1 (Ehv‐1) infection following immunization with non‐infectious L‐particles. J Microbiol 2002;40:183‐192.
  60. Mori E, Mori CM, Massironi SM. Detection of equid herpesvirus 1 DNA by polymerase chain reaction after experimental inoculation of horses with a Brazilian A4/72 strain. Braz J Vet Res Anim Sci 2009;46:253‐261.
  61. O'Neill T, Kydd JH, Allen GP, Wattrang E, Mumford JA, Hannant D. Determination of equid herpesvirus 1‐specific, CD8+, cytotoxic T lymphocyte precursor frequencies in ponies. Vet Immunol Immunopathol 1999;70:43‐54.
    pubmed: 10507286
  62. Patel JR, Földi J, Bateman H, Williams J, Didlick S, Stark R. Equid herpesvirus (EHV‐1) live vaccine strain C147: efficacy against respiratory diseases following EHV types 1 and 4 challenges. Vet Microbiol 2003;92:1‐17.
    pubmed: 12488066
  63. Patel JR, Bateman H, Williams J, Didlick S. Derivation and characterisation of a live equid herpes virus‐1 (EHV‐1) vaccine to protect against abortion and respiratory disease due to EHV‐1. Vet Microbiol 2003;91:23‐39.
    pubmed: 12441229
  64. Patel JR, Didlick S, Bateman H. Efficacy of a live equine herpesvirus‐1 (EHV‐1) strain C147 vaccine in foals with maternally‐derived antibody: protection against EHV‐1 infection. Equine Vet J 2004;36:447‐451.
    pubmed: 15253088
  65. Perkins GA, Van de Walle GR, Pusterla N. Evaluation of metaphylactic RNA interference to prevent equine herpesvirus type 1 infection in experimental herpesvirus myeloencephalopathy in horses. Am J Vet Res 2013;74:248‐256.
    pubmed: 23363350
  66. Perkins G, Babasyan S, Stout AE. Intranasal IgG4/7 antibody responses protect horses against equid herpesvirus‐1 (EHV‐1) infection including nasal virus shedding and cell‐associated viremia. Virology 2019;531:219‐232.
    pubmed: 30928700
  67. Schnabel CL, Babasyan S, Rollins A. An equine herpesvirus type 1 (EHV‐1) Ab4 open reading frame 2 deletion mutant provides immunity and protection from EHV‐1 infection and disease. J Virol 2019;93:e01011‐19.
    pmc: PMC6819910pubmed: 31462575
  68. Seahorn TL, Carter GK, Martens JG. Effects of human alpha interferon on experimentally induced equine herpesvirus‐1 infection in horses. Am J Vet Res 1990;51:2006‐2010.
    pubmed: 1964771
  69. Slater JD, Gibson JS, Field HJ. Pathogenicity of a thymidine kinase‐deficient mutant of equine herpesvirus 1 in mice and specific pathogen‐free foals. J Gen Virol 1993;74:819‐828.
    pubmed: 8388018
  70. Smith KC, Whitwell KE, Mumford JA, Hannant D, Blunden AS, Tearle JP. Virulence of the V592 isolate of equid herpesvirus‐1 in ponies. J Comp Pathol 2000;122:288‐297.
    pubmed: 10805982
  71. Soboll G, Hussey SB, Whalley JM. Antibody and cellular immune responses following DNA vaccination and EHV‐1 infection of ponies. Vet Immunol Immunopathol 2006;111:81‐95.
    pubmed: 16549215
  72. Soboll G, Breathnach CC, Kydd JH, Hussey SB, Mealey RM, Lunn DP. Vaccination of ponies with the IE gene of EHV‐1 in a recombinant modified live vaccinia vector protects against clinical and virological disease. Vet Immunol Immunopathol 2010;135:108‐117.
    pubmed: 20018383
  73. Soboll Hussey G, Hussey SB, Wagner B. Evaluation of immune responses following infection of ponies with an EHV‐1 ORF1/2 deletion mutant. Vet Res 2011;42:23.
    pmc: PMC3045331pubmed: 21314906
  74. Stokes A, Corteyn AH, Murray PK. Clinical signs and humoral immune response in horses following equine herpesvirus type‐1 infection and their susceptibility to equine herpesvirus type‐4 challenge. Res Vet Sci 1991;51:141‐148.
    pubmed: 1664967
  75. Sutton G, Thieulent C, Fortier C. 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;12:1160.
    pmc: PMC7650556pubmed: 33066315
  76. Tewari D, Gibson JS, Slater JD. Modulation of the serological response of specific pathogen‐free (EHV‐free) foals to EHV‐1 by previous infection with EHV‐4 or a TK‐deletion mutant of EHV‐1. Arch Virol 1993;132:101‐120.
    pubmed: 8394686
  77. Thieulent CJ, Sutton G, Toquet MP. Oral administration of valganciclovir reduces clinical signs, virus shedding and cell‐associated viremia in ponies experimentally infected with the equid herpesvirus‐1 C2254 variant. Pathogens 2022;11:539.
    pmc: PMC9148010pubmed: 35631060
  78. Tsujimura K, Shiose T, Yamanaka T. Equine herpesvirus type 1 mutant defective in glycoprotein E gene as candidate vaccine strain. J Vet Med Sci 2009;71:1439‐1448.
    pubmed: 19959893
  79. Van der Meulen K, Caij B, Pensaert M. Absence of viral envelope proteins in equine herpesvirus 1‐infected blood mononuclear cells during cell‐associated viremia. Vet Microbiol 2006;113:265‐273.
    pubmed: 16387454
  80. Van de Walle GR, May MA, Peters ST. A vectored equine herpesvirus type 1 (EHV‐1) vaccine elicits protective immune responses against EHV‐1 and H3N8 equine influenza virus. Vaccine 2010;28:1048‐1055.
    pubmed: 19897066
  81. Wagner B, Perkins G, Babasyan 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:e0169072.
    pmc: PMC5207648pubmed: 28045974
  82. Wimer CL, Schnabel CL, Perkins G. The deletion of the ORF1 and ORF71 genes reduces virulence of the neuropathogenic EHV‐1 strain Ab4 without host immunity in horses. PloS One 2018;13:e0206679.
    pmc: PMC6237298pubmed: 30440016
  83. Zarski LM, Weber PSD, Lee Y, Soboll HG. Transcriptomic profiling of equine and viral genes in peripheral blood mononuclear cells in horses during equine herpesvirus 1 infection. Pathogens 2021;10:43.
    pmc: PMC7825769pubmed: 33430330
  84. Pusterla N, Hussey GS, Goehring LS. Equine herpesvirus‐1 myeloencephalopathy. Vet Clin North Am Equine Pract 2022;38:339‐362.
    pubmed: 35811201
  85. Toohey‐Kurth KL, Mulrooney DM, Hinkley S. Best practices for performance of real‐time PCR assays in veterinary diagnostic laboratories. J Vet Diagn Invest 2020;32:815‐825.
    pmc: PMC7649542pubmed: 32996402