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Animals : an open access journal from MDPI2025; 15(1); 102; doi: 10.3390/ani15010102

First Molecular and Phylogenetic Characterization of Equine Herpesvirus-1 (EHV-1) and Equine Herpesvirus-4 (EHV-4) in Morocco.

Abstract: This study aimed to investigate the molecular prevalence and genetic characterization of EHV-1 and EHV-4 in equid populations in Morocco. A total of 154 equids (114 horses, 9 donkeys, and 31 mules) were sampled, with nasal swabs and tissue samples subjected to multiplex real-time PCR for the detection of EHV-1 and EHV-4. Additionally, an isolate from the tissue of an aborted horse fetus was included in the analysis. A subset of EHV-positive samples underwent virus isolation followed by whole-genome sequencing. PCR assays revealed that 42 samples (27%) tested positive for EHV-4, while only 3 samples (1.94%) were positive for EHV-1. Attempts to isolate the virus from EHV-4-positive samples were unsuccessful. However, virus isolation was successful in an EHV-1-positive nasopharyngeal sample from a donkey. Phylogenetic and molecular characterization reclassified the EHV-1 isolated from the donkey as an EHV-8. Meanwhile, the EHV-1 isolated from the aborted fetal tissue was classified as a clade 1 EHV-1 virus. This study is the first to report the molecular prevalence and genetic characterization of EHV-1 and EHV-4 in equid populations in Morocco, providing valuable insights into the distribution and genetic diversity of these viruses in the region.
Publication Date: 2025-01-05 PubMed ID: 39795045PubMed Central: PMC11718982DOI: 10.3390/ani15010102Google Scholar: Lookup
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  • 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.

Research Overview

  • This study investigates the presence and genetic makeup of Equine Herpesvirus types 1 and 4 (EHV-1 and EHV-4) in horses, donkeys, and mules in Morocco, marking the first molecular characterization of these viruses in the region.

Background and Objectives

  • Equine Herpesviruses, mainly EHV-1 and EHV-4, cause respiratory illness, abortion, and neurological disease in equids.
  • Understanding the molecular prevalence and genetic diversity of these viruses helps in disease control and epidemiology.
  • The study aims to detect the presence of EHV-1 and EHV-4 in Moroccan equid populations and characterize the viruses genetically using advanced molecular techniques.

Materials and Methods

  • Samples Collected: 154 equids consisting of 114 horses, 9 donkeys, and 31 mules.
  • Sample Types: Nasal swabs and tissue samples, including tissue from an aborted horse fetus.
  • Detection Method: Multiplex real-time PCR to identify EHV-1 and EHV-4 in samples.
  • Virus Isolation: Selected PCR-positive samples were subjected to virus isolation attempts.
  • Whole-genome Sequencing: Conducted on isolates obtained from virus-positive samples to assess genetic characteristics.

Key Findings

  • Prevalence: 42 samples (27%) were positive for EHV-4 and only 3 samples (1.94%) tested positive for EHV-1, indicating EHV-4 is more prevalent in Moroccan equids.
  • Virus Isolation Results: Attempts to isolate EHV-4 from positive samples failed, potentially due to sample quality or virus viability issues.
  • A successful virus isolation occurred from an EHV-1-positive nasopharyngeal sample from a donkey.
  • Phylogenetic Reclassification: The EHV-1 strain isolated from the donkey was genetically reclassified as EHV-8, indicating the circulation of a distinct equine herpesvirus not initially anticipated.
  • The EHV-1 isolated from the aborted fetus was classified as clade 1, a recognized group within EHV-1 viruses linked to abortion cases.

Significance and Implications

  • This is the first report detailing the molecular prevalence and genetic characterization of EHV-1 and EHV-4 in Morocco’s equids.
  • The study provides baseline data on the distribution of equine herpesviruses in this geographical region, which is crucial for disease monitoring and control strategies.
  • The detection and reclassification of an EHV-8 strain emphasize the need for broader surveillance of equine herpesviruses beyond the commonly studied EHV-1 and EHV-4.
  • The information on virus genetics may aid in understanding transmission patterns, virus evolution, and vaccine development in Moroccan and potentially broader North African equid populations.

Cite This Article

APA
El Brini Z, Cullinane A, Garvey M, Fassi Fihri O, Fellahi S, Amraoui F, Loutfi C, Sebbar G, Paillot R, Piro M. (2025). First Molecular and Phylogenetic Characterization of Equine Herpesvirus-1 (EHV-1) and Equine Herpesvirus-4 (EHV-4) in Morocco. Animals (Basel), 15(1), 102. https://doi.org/10.3390/ani15010102

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 15
Issue: 1
PII: 102

Researcher Affiliations

El Brini, Zineb
  • Department of Medicine, Surgery, and Reproduction, Agronomy and Veterinary Institute Hassan II, Rabat 10000, Morocco.
Cullinane, Ann
  • Virology Unit, The Irish Equine Centre, Johnstown, Naas, Co., W91 RH93 Kildare, Ireland.
Garvey, Marie
  • Virology Unit, The Irish Equine Centre, Johnstown, Naas, Co., W91 RH93 Kildare, Ireland.
Fassi Fihri, Ouafaa
  • Department of Microbiology, Immunology and Contagious Diseases, Agronomy and Veterinary Institute Hassan II, Rabat 10000, Morocco.
Fellahi, Siham
  • Department of Veterinary Pathology and Public Health, Agronomy and Veterinary Institute Hassan II, Rabat 10000, Morocco.
Amraoui, Farid
  • Society of Veterinary Pharmaceutical and Biological Productions (Biopharma), Rabat 10000, Morocco.
Loutfi, Chafiqa
  • Society of Veterinary Pharmaceutical and Biological Productions (Biopharma), Rabat 10000, Morocco.
Sebbar, Ghizlane
  • Society of Veterinary Pharmaceutical and Biological Productions (Biopharma), Rabat 10000, Morocco.
Paillot, Romain
  • Writtle School of Agriculture, Animal and Environmental Science, Faculty of Science and Engineering, Anglia Ruskin University, Lordship Road, Writtle, Chelmsford CM1 3RR, UK.
Piro, Mohammed
  • Department of Medicine, Surgery, and Reproduction, Agronomy and Veterinary Institute Hassan II, Rabat 10000, Morocco.

Conflict of Interest Statement

All authors declare no conflicts of interest.

References

This article includes 90 references
  1. Schoch CL, Ciufo S, Domrachev M, Hotton CL, Kannan S, Khovanskaya R, Leipe D, Mcveigh R, O’Neill K, Robbertse B. NCBI Taxonomy: A Comprehensive Update on Curation, Resources and Tools. Database J. Biol. Databases Curation 2020;2020:baaa062.
    doi: 10.1093/database/baaa062pmc: PMC7408187pubmed: 32761142google scholar: lookup
  2. Easton C, Fuentealba NA, Paullier C, Alonzo P, Carluccio J, Galosi CM. Immunohistochemical and Molecular Detection of Equine Herpesvirus 1 in Uruguay: -EN- -FR- Détection Immunohistochimique et Caractérisation Moléculaire de l’herpèsvirus Équin de Type 1 En Uruguay -ES- Detección Immunohistoquímica y Molecularcaracterización Del Herpesvirus Equino 1 En El Uruguay. Rev. Sci. Tech. OIE 2009;28:1085–1090.
    doi: 10.20506/rst.28.3.1957pubmed: 20462167google scholar: lookup
  3. Paillot R, Case R, Ross J, Newton R, Nugent J. Equine Herpes Virus-1: Virus, Immunity and Vaccines. Open Vet. Sci. J. 2008;2:68–91.
  4. Azab W, Lehmann MJ, Osterrieder N. Glycoprotein H and A4β1 Integrins Determine the Entry Pathway of Alphaherpesviruses. J. Virol. 2013;87:5937–5948.
    doi: 10.1128/JVI.03522-12pmc: PMC3648174pubmed: 23514881google scholar: lookup
  5. Oladunni FS, Horohov DW, Chambers TM. EHV-1: A Constant Threat to the Horse Industry. Front. Microbiol. 2019;10:2668.
    doi: 10.3389/fmicb.2019.02668pmc: PMC6901505pubmed: 31849857google 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. The Pathogenesis and Immune Evasive Mechanisms of Equine Herpesvirus Type 1. Front. Microbiol. 2021;12:662686.
    doi: 10.3389/fmicb.2021.662686pmc: PMC7970122pubmed: 33746936google scholar: lookup
  7. Ma G, Azab W, Osterrieder N. Equine Herpesviruses Type 1 (EHV-1) and 4 (EHV-4)—Masters of Co-Evolution and a Constant Threat to Equids and Beyond. Vet. Microbiol. 2013;167:123–134.
    doi: 10.1016/j.vetmic.2013.06.018pubmed: 23890672google scholar: lookup
  8. Allen GP, Kydd JH, Slater JD, Smith KC. Equid herpesvirus 1 (EHV-1) and equid herpesvirus 4 (EHV-4) infections. In: Coetzer J.A.W., Tustin R.C., editors. Infectious Diseases of Livestock. Oxford Press; Cape Town, South Africa: 2004. pp. 829–859. Chapter 76.
  9. Hussey G, Goehring LS, Lunn DP, Hussey SB, Huang T, Osterrieder N, Powell C, Hand J, Holz C, Slater J. Experimental Infection with Equine Herpesvirus Type 1 (EHV-1) Induces Chorioretinal Lesions. Vet. Res. 2013;44:118.
    doi: 10.1186/1297-9716-44-118pmc: PMC4028784pubmed: 24308772google scholar: lookup
  10. Lunn DP, Burgess BA, Dorman DC, Goehring LS, Gross P, Osterrieder K, Pusterla N, Soboll Hussey G. Updated ACVIM consensus statement on equine herpesvirus-1. J. Vet. Intern. Med. 2024;38:1290–1299.
    doi: 10.1111/jvim.17047pmc: PMC11099706pubmed: 38497217google scholar: lookup
  11. 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.
    doi: 10.1016/j.vetmic.2006.11.009pubmed: 17208393google scholar: lookup
  12. Osterrieder N, Van de Walle GR. Pathogenic Potential of Equine Alphaherpesviruses: The Importance of the Mononuclear Cell Compartment in Disease Outcome. Vet. Microbiol. 2010;143:21–28.
    doi: 10.1016/j.vetmic.2010.02.010pubmed: 20202764google scholar: lookup
  13. Pusterla N, Hussey GS. Equine Herpesvirus 1 Myeloencephalopathy. Vet. Clin. N. Am. Equine Pract. 2014;30:489–506.
    doi: 10.1016/j.cveq.2014.08.006pubmed: 25300635google scholar: lookup
  14. Borchers K, Wolfinger U, Ludwig H. Latency-Associated Transcripts of Equine Herpesvirus Type 4 in Trigeminal Ganglia of Naturally Infected Horses. J. Gen. Virol. 1999;80:2165–2171.
    doi: 10.1099/0022-1317-80-8-2165pubmed: 10466816google scholar: lookup
  15. Slater JD, Borchers K, Thackray AM, Field HJ. The Trigeminal Ganglion Is a Location for Equine Herpesvirus 1 Latency and Reactivation in the Horse. J. Gen. Virol. 1994;75:2007–2016.
    doi: 10.1099/0022-1317-75-8-2007pubmed: 8046404google scholar: lookup
  16. Welch HM, Bridges CG, Lyon AM, Griffiths L, Edington N. Latent Equid Herpesviruses 1 and 4: Detection and Distinction Using the Polymerase Chain Reaction and Co-Cultivation from Lymphoid Tissues. J. Gen. Virol. 1992;73:261–268.
    doi: 10.1099/0022-1317-73-2-261pubmed: 1347078google scholar: lookup
  17. Gilkerson JR, Bailey KE, Diaz-Méndez A, Hartley CA. Update on Viral Diseases of the Equine Respiratory Tract. Vet. Clin. N. Am. Equine Pract. 2015;31:91–104.
    doi: 10.1016/j.cveq.2014.11.007pubmed: 25648568google scholar: lookup
  18. Bannai H, Nemoto M, Tsujimura K, Yamanaka T, Kondo T, Matsumura T. Development of a Focus-Reduction Neutralizing Test for Detecting Equine Herpesvirus Type-1-Neutralizing Antibodies. J. Vet. Med. Sci. 2013;75:1209–1212.
    doi: 10.1292/jvms.13-0043pubmed: 23595119google scholar: lookup
  19. Lang A, de Vries M, Feineis S, Müller E, Osterrieder N, Damiani AM. Development of a Peptide ELISA for Discrimination between Serological Responses to Equine Herpesvirus Type 1 and 4. J. Virol. Methods. 2013;193:667–673.
  20. Balasuriya UBR, Crossley BM, Timoney PJ. A Review of Traditional and Contemporary Assays for Direct and Indirect Detection of Equid Herpesvirus 1 in Clinical Samples. J. Vet. Diagn. Investig. 2015;27:673–687.
    doi: 10.1177/1040638715605558pubmed: 26472746google scholar: lookup
  21. 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.
  22. Borchers K, Slater J. A Nested PCR for the Detection and Differentiation of EHV-1 and EHV-4. J. Virol. Methods. 1993;45:331–336.
    doi: 10.1016/0166-0934(93)90117-Apubmed: 8106604google scholar: lookup
  23. Carvalho R, Passos LMF, Martins AS. Development of a Differential Multiplex PCR Assay for Equine Herpesvirus 1 and 4 as a Diagnostic Tool. J. Vet. Med. Ser. B. 2000;47:351–359.
  24. Diallo IS, Hewitson G, Wright LL, Kelly MA, Rodwell BJ, Corney BG. Multiplex Real-Time PCR for the Detection and Differentiation of Equid Herpesvirus 1 (EHV-1) and Equid Herpesvirus 4 (EHV-4). Vet. Microbiol. 2007;123:93–103.
    doi: 10.1016/j.vetmic.2007.02.004pubmed: 17346907google scholar: lookup
  25. Kirisawa R, Endo A, Iwai H, Kawakami Y. Detection and Identification of Equine Herpesvirus-1 and -4 by Polymerase Chain Reaction. Vet. Microbiol. 1993;36:57–67.
    doi: 10.1016/0378-1135(93)90128-Tpubmed: 8236780google scholar: lookup
  26. Lawrence GL, Gilkerson J, Love DN, Sabine M, Whalley JM. Rapid, Single-Step Differentiation of Equid Herpesviruses 1 and 4 from Clinical Material Using the Polymerase Chain Reaction and Virus-Specific Primers. J. Virol. Methods. 1994;47:59–72.
    doi: 10.1016/0166-0934(94)90066-3pubmed: 8051234google scholar: lookup
  27. Varrasso A, Dynon K, Ficorilli N, Hartley C, Studdert M, Drummer H. Identification of Equine Herpesviruses 1 and 4 by Polymerase Chain Reaction. Aust. Vet. J. 2001;79:563–569.
  28. Henry BE, Robinson RA, Dauenhauer SA, Atherton SS, Hayward GS, O’Callaghan DJ. Structure of the Genome of Equine Herpesvirus Type 1. Virology 1981;115:97–114.
    doi: 10.1016/0042-6822(81)90092-1pubmed: 6270904google scholar: lookup
  29. Pellett PE, Roizman B. Herpesviridae: A Brief Introduction. In: Howley PM, editor. Fields Virology. 5th ed. Lippincott, Williams and Wilkins; Philadelphia, PA, USA: 2007. pp. 2480–2499.
  30. Telford EAR, Watson MS, McBride K, Davison AJ. The DNA Sequence of Equine Herpesvirus-1. Virology 1992;189:304–316.
    doi: 10.1016/0042-6822(92)90706-Upubmed: 1318606google scholar: lookup
  31. Whalley JM, Robertson GR, Davison AJ. Analysis of the Genome of Equine Herpesvirus Type 1: Arrangement of Cleavage Sites for Restriction Endonucleases EcoRI, BglII and BamHI. J. Gen. Virol. 1981;57:307–323.
    doi: 10.1099/0022-1317-57-2-307pubmed: 6275028google scholar: lookup
  32. Yalamanchili RR, O’Callaghan DJ. Sequence and Organization of the Genomic Termini of Equine Herpesvirus Type 1. Virus Res. 1990;15:149–161.
    doi: 10.1016/0168-1702(90)90005-Vpubmed: 2157316google scholar: lookup
  33. Laabassi F, Hue E, Fortier C, Morilland E, Legrand L, Hans A, Pronost S. Epidemiology and Molecular Detection of Equine Herpesviruses in Western Algeria in 2011. Vet. Microbiol. 2017;207:205–209.
    doi: 10.1016/j.vetmic.2017.06.017pubmed: 28757025google scholar: lookup
  34. Badr C, Souiai O, Arbi M, El Behi I, Essaied MS, Khosrof I, Benkahla A, Chabchoub A, Ghram A. Epidemiological and Phylogeographic Study of Equid Herpesviruses in Tunisia. Pathogens 2022;11:1016.
    doi: 10.3390/pathogens11091016pmc: PMC9504996pubmed: 36145448google scholar: lookup
  35. Wagner WN, Bogdan J, Haines D, Townsend HGG, Misra V. Detection of Equine Herpesvirus and Differentiation of Equine Herpesvirus Type 1 from Type 4 by the Polymerase Chain Reaction. Can. J. Microbiol. 1992;38:1193–1196.
    doi: 10.1139/m92-196pubmed: 1335829google scholar: lookup
  36. Diallo IS, Hewitson G, Wright L, Rodwell BJ, Corney BG. Detection of Equine Herpesvirus Type 1 Using a Real-Time Polymerase Chain Reaction. J. Virol. Methods. 2006;131:92–98.
  37. JPM Pro 17.0.0. JMP Statistical Discovery LLC 2022, SAS Campus Drive; Cary, NC, USA: 2022.
  38. Garvey M, Lyons R, Hector R, 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;8:7.
    doi: 10.3390/pathogens8010007pmc: PMC6471309pubmed: 30650561google scholar: lookup
  39. Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R. Clustal W and Clustal X Version 2.0. Bioinformatics 2007;23:2947–2948.
    doi: 10.1093/bioinformatics/btm404pubmed: 17846036google scholar: lookup
  40. Hall TA. BioEdit: A User-Friendly Biological Sequence Alignment Editor and Analysis Program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 1999;41:95–98.
  41. Vereecke N, Carnet F, Pronost S, Vanschandevijl K, Theuns S, Nauwynck H. Genome Sequences of Equine Herpesvirus 1 Strains from a European Outbreak of Neurological Disorders Linked to a Horse Gathering in Valencia, Spain, in 2021. Microbiol. Resour. Announc. 2021;10:e00333-21.
    doi: 10.1128/MRA.00333-21pmc: PMC8188346pubmed: 34016681google scholar: lookup
  42. Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies. Mol. Biol. Evol. 2015;32:268–274.
    doi: 10.1093/molbev/msu300pmc: PMC4271533pubmed: 25371430google scholar: lookup
  43. Letunic I, Bork P. Interactive Tree Of Life (ITOL): An Online Tool for Phylogenetic Tree Display and Annotation. Bioinformatics 2007;23:127–128.
    doi: 10.1093/bioinformatics/btl529pubmed: 17050570google scholar: lookup
  44. Bryant NA, Wilkie GS, Russell CA, Compston L, Grafham D, Clissold L, McLay K, Medcalf L, Newton R, Davison AJ. Genetic Diversity of Equine Herpesvirus 1 Isolated from Neurological, Abortigenic and Respiratory Disease Outbreaks. Transbound. Emerg. Dis. 2018;65:817–832.
    doi: 10.1111/tbed.12809pmc: PMC5947664pubmed: 29423949google scholar: lookup
  45. Darling ACE, Mau B, Blattner FR, Perna NT. Mauve: Multiple Alignment of Conserved Genomic Sequence With Rearrangements. Genome Res. 2004;14:1394–1403.
    doi: 10.1101/gr.2289704pmc: PMC442156pubmed: 15231754google scholar: lookup
  46. Guindon S, Gascuel O. A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood. Syst. Biol. 2003;52:696–704.
    doi: 10.1080/10635150390235520pubmed: 14530136google scholar: lookup
  47. Simão FA, Waterhouse RM, Ioannidis P, Kriventseva EV, Zdobnov EM. BUSCO: Assessing Genome Assembly and Annotation Completeness with Single-Copy Orthologs. Bioinformatics 2015;31:3210–3212.
    doi: 10.1093/bioinformatics/btv351pubmed: 26059717google scholar: lookup
  48. Jain C, Rodriguez-R LM, Phillippy AM, Konstantinidis KT, Aluru S. High Throughput ANI Analysis of 90K Prokaryotic Genomes Reveals Clear Species Boundaries. Nat. Commun. 2018;9:5114.
    doi: 10.1038/s41467-018-07641-9pmc: PMC6269478pubmed: 30504855google scholar: lookup
  49. Pusterla N, Mapes S, Akana N, Barnett C, MacKenzie C, Gaughan E, Craig B, Chappell D, Vaala W. 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.
    doi: 10.1136/vr.103424pubmed: 26607427google scholar: lookup
  50. Ko S, Kang JG, Yeh JY, Moon JS, Choi GC, Won S, Chae JS. First Report on Molecular Detection of Equine Upper Respiratory Infectious Viruses in Republic of Korea. J. Equine Vet. Sci. 2013;33:628–636.
  51. Negussie H, Gizaw D, Tesfaw L, Li Y, Oguma K, Sentsui H, Tessema TS, Nauwynck HJ. Detection of Equine Herpesvirus (EHV) -1, -2, -4 and -5 in Ethiopian Equids with and without Respiratory Problems and Genetic Characterization of EHV-2 and EHV-5 Strains. Transbound. Emerg. Dis. 2017;64:1970–1978.
    doi: 10.1111/tbed.12601pubmed: 28102009google scholar: lookup
  52. Seo MG, Ouh IO, Lee SK, Lee JS, Kwon OD, Kwak D. Molecular Detection and Genetic Characteristics of Equine Herpesvirus in Korea. Pathogens 2020;9:110.
    doi: 10.3390/pathogens9020110pmc: PMC7168308pubmed: 32053974google scholar: lookup
  53. Taktaz Hafshejani T, Nekoei S, Vazirian B, Doosti A, Khamesipour F, Anyanwu MU. Molecular Detection of Equine Herpesvirus Types 1 and 4 Infection in Healthy Horses in Isfahan Central and Shahrekord Southwest Regions, Iran. BioMed Res. Int. 2015;2015:1–7.
    doi: 10.1155/2015/917854pmc: PMC4569764pubmed: 26421307google scholar: lookup
  54. Izume S, Kirisawa R, Ohya K, Ohnuma A, Kimura T, Omatsu T, Katayama Y, Mizutani T, Fukushi H. The Full Genome Sequences of 8 Equine Herpesvirus Type 4 Isolates from Horses in Japan. J. Vet. Med. Sci. 2017;79:206–212.
    doi: 10.1292/jvms.16-0506pmc: PMC5289262pubmed: 27840393google scholar: lookup
  55. Patel JR, Heldens J. Equine Herpesviruses 1 (EHV-1) and 4 (EHV-4)—Epidemiology, Disease and Immunoprophylaxis: A Brief Review. Vet. J. 2005;170:14–23.
    doi: 10.1016/j.tvjl.2004.04.018pubmed: 15993786google scholar: lookup
  56. Turan N, Yildirim F, Altan E, Sennazli G, Gurel A, Diallo I, Yilmaz H. Molecular and Pathological Investigations of EHV-1 and EHV-4 Infections in Horses in Turkey. Res. Vet. Sci. 2012;93:1504–1507.
    doi: 10.1016/j.rvsc.2012.01.019pubmed: 22401978google scholar: lookup
  57. Pavulraj S, Eschke K, Theisen J, Westhoff S, Reimers G, Andreotti S, Osterrieder N, Azab W. Equine Herpesvirus Type 4 (EHV-4) Outbreak in Germany: Virological, Serological, and Molecular Investigations. Pathogens 2021;10:810.
    doi: 10.3390/pathogens10070810pmc: PMC8308676pubmed: 34202127google scholar: lookup
  58. Matsumura T, Sugiura T, Imagawa H, Fukunaga Y, Kamada M. Epizootiological Aspects of Type 1 and Type 4 Equine Herpesvirus Infections among Horse Populations. J. Vet. Med. Sci. 1992;54:207–211.
    doi: 10.1292/jvms.54.207pubmed: 1318750google scholar: lookup
  59. El Brini Z, Fassi Fihri O, Paillot R, Lotfi C, Amraoui F, El Ouadi H, Dehhaoui M, Colitti B, Alyakine H, Piro M. Seroprevalence of Equine Herpesvirus 1 (EHV-1) and Equine Herpesvirus 4 (EHV-4) in the Northern Moroccan Horse Populations. Animals 2021;11:2851.
    doi: 10.3390/ani11102851pmc: PMC8532652pubmed: 34679874google scholar: lookup
  60. Getachew M, Alemayehu F, Chala C, Amare B, Kassa D, Burden F, Wernery R, Wernery U. A Cross-Sectional Sero-Survey of Some Infectious Diseases of Working Equids in Central Ethiopia. J. Vet. Med. Anim. Health. 2014;6:231–238.
  61. Yildirim Y, Yilmaz V, Kirmizigul AH. Equine herpesvirus type 1 (EHV-1) and 4 (EHV-4) infections in horses and donkeys in northeastern Turkey. Iran. J. Vet. Res. 2015;16:341–344.
    pmc: PMC4782672pubmed: 27175200
  62. Foote CE, Love DN, Gilkerson JR, Whalley JM. Detection of EHV-1 and EHV-4 DNA in Unweaned Thoroughbred Foals from Vaccinated Mares on a Large Stud Farm. Equine Vet. J. 2004;36:341–345.
    doi: 10.2746/0425164044890634pubmed: 15163042google scholar: lookup
  63. de Souza Hunol Lara MdCC, Villalobos EMC, Cunha EMS, de Oliveira JV, de Castro Nassar AF, Silva LMP, Okuda LH, de Campos Nogueira Romaldini AH, Cunha MS, Marques EC. Occurrence of Viral Diseases in Donkeys (Equus Asinus) in São Paulo State, Brazil. Braz. J. Vet. Res. Anim. Sci. 2017;54:154.
  64. Pusterla N, Mapes S, Wademan C, White A, Estell K, Swain E. Investigation of the Role of Mules as Silent Shedders of EHV-1 during an Outbreak of EHV-1 Myeloencephalopathy in California. Vet. Rec. 2012;170:465.
    doi: 10.1136/vr.100598pubmed: 22472540google scholar: lookup
  65. Slater J. Equine Herpesviruses. In: Sellon DC, Long MT, editors. Equine Infectious Diseases. Saunders Elsevier; St. Louis, MO, USA: 2007. pp. 134–153.
  66. Ploszay G, Rola J, Larska M, Zmudzinski JF. First Report on Equine Herpesvirus Type 4 Isolation in Poland—Evaluation of Diagnostic Tools. Pol. J. Vet. Sci. 2013;16:493–500.
    doi: 10.2478/pjvs-2013-0069pubmed: 24195284google scholar: lookup
  67. Burgess BA, Tokateloff N, Manning S, Lohmann K, Lunn DP, Hussey SB, Morley PS. Nasal Shedding of Equine Herpesvirus-1 from Horses in an Outbreak of Equine Herpes Myeloencephalopathy in W Estern C Anada. J. Vet. Intern. Med. 2012;26:384–392.
  68. Marenzoni ML, Passamonti F, Cappelli K, Veronesi F, Capomaccio S, Verini Supplizi A, Valente C, Autorino G, Coletti M. Clinical, Serological and Molecular Investigations of EHV-1 and EHV-4 in 15 Unweaned Thoroughbred Foals. Vet. Rec. 2008;162:337–341.
    doi: 10.1136/vr.162.11.337pubmed: 18344498google scholar: lookup
  69. Dynon K, Black W, Ficorilli N, Hartley C, Studdert M. Detection of Viruses in Nasal Swab Samples from Horses with Acute, Febrile, Respiratory Disease Using Virus Isolation, Polymerase Chain Reaction and Serology. Aust. Vet. J. 2007;85:46–50.
  70. Stasiak K, Dunowska M, Hills SF, Rola J. Genetic Characterization of Equid Herpesvirus Type 1 from Cases of Abortion in Poland. Arch. Virol. 2017;162:2329–2335.
    doi: 10.1007/s00705-017-3376-3pmc: PMC5506511pubmed: 28451902google scholar: lookup
  71. 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 C2254/H752 Strain in French Horses Showing No Major Impact on the Strain Behaviour. Viruses 2020;12:1160.
    doi: 10.3390/v12101160pmc: PMC7650556pubmed: 33066315google scholar: lookup
  72. Gradzki Z, Boguta L. Use of PCR and Cell Culture Method in the Diagnosis and Differentiation of EHV1 and EHV4 Infections in Horses. Med. Weter. 2009;65:546–551.
  73. Diallo IS, Hewitson GR, de Jong A, Kelly MA, Wright DJ, Corney BG, Rodwell BJ. Equine Herpesvirus Infections in Yearlings in South-East Queensland. Arch. Virol. 2008;153:1643–1649.
    doi: 10.1007/s00705-008-0158-ypubmed: 18677574google scholar: lookup
  74. Afify AF, Ahmed BM, Salem SA, El-Sanousi AA. First Isolation and Identification of EHV-4 during Abortion Outbreak among Arabian Horses in Egypt Reflects an Alteration in Pathogenic Potentiality of EHV-4. J. Virol. Sci. 2017;2:92–101.
  75. Gryspeerdt AC, Vandekerckhove AP, Garré B, Barbé F, Van de Walle GR, Nauwynck HJ. 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.
    doi: 10.1016/j.vetmic.2009.10.015pubmed: 19926232google scholar: lookup
  76. Rimstad E, Evensen Ø. The Identification of Equid Herpesvirus 1 in Paraffin-Embedded Tissues from Aborted Fetuses by Polymerase Chain Reaction and Immunohistochemistry. J. Vet. Diagn. Investig. 1993;5:174–183.
    doi: 10.1177/104063879300500206pubmed: 8389598google scholar: lookup
  77. 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:e0192301.
  78. Browning GF, Ficorilli N, Studdert MJ. Asinine Herpesvirus Genomes: Comparison with Those of the Equine Herpesviruses. Arch. Virol. 1988;101:183–190.
    doi: 10.1007/BF01310999pubmed: 2845891google scholar: lookup
  79. van Maanen K, van der Zaag E, Buter R, van den Wollenberg L, van Oldruitenborgh-Oosterbaan MS. Asinine Herpesvirus-3 (Equine Herpesvirus-8)-associated Neurological Disease in a Donkey. Vet. Rec. Case Rep. 2017;5:e000498.
  80. Wang T, Hu L, Wang Y, Liu W, Liu G, Zhu M, Zhang W, Wang C, Ren H, Li L. Identification of Equine Herpesvirus 8 in Donkey Abortion: A Case Report. Virol. J. 2022;19:10.
    doi: 10.1186/s12985-021-01738-2pmc: PMC8734136pubmed: 34991640google scholar: lookup
  81. MAPMDREF Annuaire Statistique Du Maroc, Format Excel. Site Institutionnel Du Haut-Commissariat Au Plan Du Royaume Du Maroc. Consulté à L’adresse: 2021. [(accessed on 28 January 2024)]. Available online: https://www.hcp.ma/downloads/annuaire-statistique-du-maroc-format-excel_t22392.html.
  82. 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;80:4047–4060.
  83. Sutton G, Garvey M, Cullinane A, Jourdan M, Fortier C, Moreau P, Foursin M, Gryspeerdt A, Maisonnier V, Marcillaud-Pitel C. 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.
    doi: 10.3390/v11100916pmc: PMC6832873pubmed: 31590336google scholar: lookup
  84. Sutton G, Normand C, Carnet F, Couroucé A, Garvey M, Castagnet S, Fortier CI, Hue ES, Marcillaud-Pitel C, Legrand L. Equine Herpesvirus 1 Variant and New Marker for Epidemiologic Surveillance, Europe, 2021. Emerg. Infect. Dis. 2021;27:2738–2739.
    doi: 10.3201/eid2710.210704pmc: PMC8462333pubmed: 34546162google scholar: lookup
  85. 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.2019.00059pmc: PMC6409500pubmed: 30886853google scholar: lookup
  86. Vandekerckhove AP, Glorieux S, Gryspeerdt AC, Steukers L, Van Doorsselaere J, Osterrieder N, Van de Walle GR, Nauwynck HJ. Equine Alphaherpesviruses (EHV-1 and EHV-4) Differ in Their Efficiency to Infect Mononuclear Cells during Early Steps of Infection in Nasal Mucosal Explants. Vet. Microbiol. 2011;152:21–28.
    doi: 10.1016/j.vetmic.2011.03.038pubmed: 21536394google scholar: lookup
  87. Cuxson JL, Hartley CA, Ficorilli NP, Symes SJ, Devlin JM, Gilkerson JR. Comparing the Genetic Diversity of ORF30 of Australian Isolates of 3 Equid Alphaherpesviruses. Vet. Microbiol. 2014;169:50–57.
    doi: 10.1016/j.vetmic.2013.12.007pubmed: 24418044google scholar: lookup
  88. Perkins GA, Goodman LB, Tsujimura K, Van de Walle GR, Kim SG, Dubovi EJ, Osterrieder N. Investigation of the Prevalence of Neurologic Equine Herpes Virus Type 1 (EHV-1) in a 23-Year Retrospective Analysis (1984–2007). Vet. Microbiol. 2009;139:375–378.
    doi: 10.1016/j.vetmic.2009.06.033pubmed: 19615831google scholar: lookup
  89. Pronost S, Cook RF, Fortier G, Timoney PJ, Balasuriya UBR. Relationship between Equine Herpesvirus-1 Myeloencephalopathy and Viral Genotype. Equine Vet. J. 2010;42:672–674.
  90. Vissani MA, Becerra ML, Olguín Perglione C, Tordoya MS, Miño S, Barrandeguy M. Neuropathogenic and Non-Neuropathogenic Genotypes of Equid Herpesvirus Type 1 in Argentina. Vet. Microbiol. 2009;139:361–364.
    doi: 10.1016/j.vetmic.2009.06.025pubmed: 19589651google scholar: lookup

Citations

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  1. Kutumbetov L, Myrzakhmetova B, Tussipova A, Zhapparova G, Tlenchiyeva T, Bissenbayeva K, Nurabayev S, Kerimbayev A. Development and Preclinical Evaluation of a Lyophilized Vaccine Against Equine Herpesvirus Type 4 (EHV-4).. Vaccines (Basel) 2025 May 31;13(6).
    doi: 10.3390/vaccines13060604pubmed: 40573935google scholar: lookup
  2. Ji Y, Xu D, Si W, Zhang Y, Khan MZ, Zhao X, Liu W. Characterization and Pathogenicity of Equine Herpesvirus Type 8 Using In-Vitro and In-Vivo Models.. Vet Sci 2025 Apr 15;12(4).
    doi: 10.3390/vetsci12040367pubmed: 40284869google scholar: lookup