Analyze Diet
Viruses2022; 14(4); doi: 10.3390/v14040713

Kinetics of the Equid Herpesvirus 2 and 5 Infections among Mares and Foals from Three Polish National Studs.

Abstract: Equid herpesvirus 2 (EHV-2) and 5 (EHV-5) are two γ-herpesviruses that are commonly detected from horses worldwide, based on several cross-sectional molecular surveys. Comparatively few studies examined the dynamics of γ-herpesvirus infection over time in a group of horses. The aim of the current study was to investigate the dynamics of EHV-2/5 infections among mares and their foals at three Polish national studs with different breeds of horses: Arabians, Thoroughbreds and Polish Konik horses. Nasal swabs were collected from each of 38 mare-foal pairs monthly for a period of 6 to 8 months. Virus-specific quantitative PCR assays were used to determine the viral load of EHV-2 and EHV-5 in each sample. All 76 horses sampled were positive for EHV-2 or EHV-5 on at least one sampling occasion. The majority (73/76, 96%) were infected with both EHV-2 and EHV-5. In general, the mean load of viral DNA was higher in samples from foals than from mares, but similar for EHV-2 and EHV-5 at most sampling occasions. There was, however, a considerable variability in the viral DNA load between samples collected at different times from the same foal, as well as between samples from different foals. The latter was more apparent for EHV-2 than for EHV-5. All foals became infected with both viruses early in life, before weaning, and remained positive on all, or most, subsequent samplings. The virus shedding by mares was more intermittent, indicating the existence of age-related differences. Overall, the data presented extend our knowledge of EHV-2/5 epidemiology among mares and foals.
Publication Date: 2022-03-29 PubMed ID: 35458443PubMed Central: PMC9031536DOI: 10.3390/v14040713Google 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 study focuses on understanding the dynamics of Equid herpesvirus 2 (EHV-2) and 5 (EHV-5) infections in mares and their foals from different breeds, at three Polish national stud farms over time.

Dynamics of EHV-2/5 Infections

  • The study aimed to investigate the infection dynamics between EHV-2 and 5 in different horse breeds in Poland – Arabians, Thoroughbreds and Polish Konik horses.
  • Virus-specific quantitative PCR assays were used to determine the viral load of EHV-2 and EHV-5 in each sample collected.
  • In total, 76 horses (38 mare-foal pairs) were involved in the study. Out of these, all horses were found to have at least one instance of either EHV-2 or EHV-5.
  • Results showed a heavy prevalence of EHV-2 and 5 among the sampled horses, with 96% (73 out of 76) found to be infected by both viruses at some point.

Variances in Viral Loads

  • The mean viral DNA load was observed to be higher in samples taken from foals than from mares, however, the load was similar for both types of viruses across sampling occasions.
  • Samples collected from the same foal at different times showed considerable variability in viral DNA load, as well as between samples from different foals.
  • Higher variability in viral DNA loads was detected for EHV-2 than for EHV-5.

Age-Related Differences in Virus Shedding

  • All foals became infected with both viruses early in life, before weaning, and remained positive during most of the subsequent samplings.
  • Viral shedding in mares was found to be more intermittent, highlighting the existence of age-related differences in virus shedding.

Outcome of the Study

  • The presented data from the current study added further insights into the epidemiology of EHV-2/5 in mare and foal cohorts.
  • The study underscores the high prevalence of EHV-2/5 in the horse population and points towards the need for further investigation to better understand the infection dynamics over time.

Cite This Article

APA
Stasiak K, Dunowska M, Rola J. (2022). Kinetics of the Equid Herpesvirus 2 and 5 Infections among Mares and Foals from Three Polish National Studs. Viruses, 14(4). https://doi.org/10.3390/v14040713

Publication

ISSN: 1999-4915
NlmUniqueID: 101509722
Country: Switzerland
Language: English
Volume: 14
Issue: 4

Researcher Affiliations

Stasiak, Karol
  • Department of Virology, National Veterinary Research Institute, 24-100 Pulawy, Poland.
Dunowska, Magdalena
  • School of Veterinary Science, Massey University, Palmerston North 4442, New Zealand.
Rola, Jerzy
  • Department of Virology, National Veterinary Research Institute, 24-100 Pulawy, Poland.

MeSH Terms

  • Animals
  • Cross-Sectional Studies
  • DNA, Viral / genetics
  • Female
  • Herpesviridae Infections
  • Herpesvirus 1, Equid / genetics
  • Herpesvirus 4, Equid / genetics
  • Horse Diseases
  • Horses
  • Kinetics
  • Poland / epidemiology
  • Rhadinovirus / genetics

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 48 references
  1. Marenzoni M.L., Coppola G., Maranesi M., Passamonti F., Cappelli K., Capomaccio S., Verini Supplizi A., Thiry E., Coletti M.. Age-dependent prevalence of equid herpesvirus 5 infection.. Vet. Res. Commun. 2010;34:703–708.
    doi: 10.1007/s11259-010-9443-9pubmed: 20842426google scholar: lookup
  2. Wang L., Raidal S.L., Pizzirani A., Wilcox G.E.. 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
  3. Hue E.S., Fortier G.D., Fortier C.I., Leon A.M., Richard E.A., Legrand L.J., Pronost S.L.. Detection and quantitation of equid gammaherpesviruses (EHV-2, EHV-5) in nasal swabs using an accredited standardised quantitative PCR method.. J. Virol. Methods. 2014;198:18–25.
  4. Brault S.A., Maclachlan N.J.. Equid gammaherpesviruses: Persistent bystanders or true pathogens?. Vet. J. 2011;187:14–15.
    doi: 10.1016/j.tvjl.2010.02.015pubmed: 20335057google scholar: lookup
  5. Dunowska M., Meers J., Wilks C.. Isolation of equine herpesvirus type 5 in New Zealand.. N. Z. Vet. J. 1999;47:44–46.
    doi: 10.1080/00480169.1999.36109pubmed: 16032069google scholar: lookup
  6. Bell S.A., Balasuriya U.B., Gardner I.A., Barry P.A., Wilson W.D., Ferraro G.L., MacLachlan N.J.. Temporal detection of equine herpesvirus infections of a cohort of mares and their foals.. Vet. Microbiol. 2006;116:249–257.
    doi: 10.1016/j.vetmic.2006.05.002pubmed: 16774810google scholar: lookup
  7. Dunowska M., Wilks C., Studdert M., Meers J.. Viruses associated with outbreaks of equine respiratory disease in New Zealand.. N. Z. Vet. J. 2002;50:132–139.
    doi: 10.1080/00480169.2002.36299pubmed: 16032259google scholar: lookup
  8. Marenzoni M.L., Stefanetti V., Danzetta M.L., Timoney P.J.. Gammaherpesvirus infections in equids: A review.. Vet. Med. 2015;6:91–101.
    doi: 10.2147/VMRR.S39473pmc: PMC6065615pubmed: 30155436google scholar: lookup
  9. Fortier G., van Erck E., Fortier C., Richard E., Pottier D., Pronost S., Miszczak F., Thiry E., Lekeux P.. Herpesviruses in respiratory liquids of horses: Putative implication in airway inflammation and association with cytological features.. Vet. Microbiol. 2009;139:34–41.
    doi: 10.1016/j.vetmic.2009.04.021pubmed: 19427139google scholar: lookup
  10. Fortier G., Richard E., Hue E., Fortier C., Pronost S., Pottier D., Lemaitre L., Lekeux P., Borchers K., Thiry E.. Long-lasting airway inflammation associated with equid herpesvirus-2 in experimentally challenged horses.. Vet. J. 2013;197:492–495.
    doi: 10.1016/j.tvjl.2012.12.027pubmed: 23433569google scholar: lookup
  11. Houtsma A., Bedenice D., Pusterla N., Pugliese B., Mapes S., Hoffman A.M., Paxson J., Rozanski E., Mukherjee J., Wigley M.. Association between inflammatory airway disease of horses and exposure to respiratory viruses: A case control study.. Multidiscip. Respir. Med. 2015;10:33.
    doi: 10.1186/s40248-015-0030-3pmc: PMC4630835pubmed: 26535117google scholar: lookup
  12. Fortier G., Pronost S., Miszczak F., Fortier C., Léon A., Richard E., Van Erck E., Thiry E., Lekeux P.. Identification of equid herpesvirus-5 in respiratory liquids: A retrospective study of 785 samples taken in 2006–2007.. Vet. J. 2009;182:346–348.
    doi: 10.1016/j.tvjl.2008.07.004pubmed: 18757217google scholar: lookup
  13. Back H., Ullman K., Berndtsson L.T., Riihimäki M., Penell J., Ståhl K., Valarcher J.-F., Pringle J.. Viral load of equine herpesviruses 2 and 5 in nasal swabs of actively racing Standardbred trotters: Temporal relationship of shedding to clinical findings and poor performance.. Vet. Microbiol. 2015;179:142–148.
    doi: 10.1016/j.vetmic.2015.06.002pubmed: 26093774google scholar: lookup
  14. Hartley C.A., Dynon K.J., Mekuria Z.H., El-Hage C.M., Holloway S.A., Gilkerson J.R.. Equine gammaherpesviruses: Perfect parasites?. Vet. Microbiol. 2013;167:86–92.
    doi: 10.1016/j.vetmic.2013.05.031pubmed: 23845734google scholar: lookup
  15. Nordengrahn A., Rusvai M., Merza M., Ekstrom J., Morein B., Belak S.. Equine herpesvirus type 2 (EHV-2) as a predisposing factor for rhodococcus equi pneumonia in foals: Prevention of the bifactorial disease with EHV-2 immunostimulating complexes.. Vet. Microbiol. 1996;51:55–68.
    doi: 10.1016/0378-1135(96)00032-6pubmed: 8828122google scholar: lookup
  16. Brault S.A., Blanchard M.T., Gardner I.A., Stott J.L., Pusterla N., Mapes S.M., Vernau W., Dejong K.D., Maclachlan N.J.. The immune response of foals to natural infection with equid herpesvirus-2 and its association with febrile illness.. Vet. Immunol. Immunopathol. 2010;137:136–141.
    doi: 10.1016/j.vetimm.2010.05.010pubmed: 20646766google scholar: lookup
  17. Brault S.A., Bird B.H., Balasuriya U.B., MacLachlan N.J.. Genetic heterogeneity and variation in viral load during equid herpesvirus-2 infection of foals.. Vet. Microbiol. 2011;147:253–261.
    doi: 10.1016/j.vetmic.2010.06.031pubmed: 20655670google scholar: lookup
  18. Browning G.F., Studdert M.J.. Genomic heterogeneity of equine betaherpesviruses.. J. Gen. Virol. 1987;68:1441–1447.
    doi: 10.1099/0022-1317-68-5-1441pubmed: 2883251google scholar: lookup
  19. Dunowska M., Holloway S.A., Wilks C.R., Meers J.. Genomic variability of equine herpesvirus-5.. Arch. Virol. 2000;145:1359–1371.
    doi: 10.1007/s007050070095pubmed: 10963342google scholar: lookup
  20. Kershaw O., von Oppen T., Glitz F., Deegen E., Ludwig H., Borchers K.. Detection of equine herpesvirus type 2 (EHV-2) in horses with keratoconjunctivitis.. Virus Res. 2001;80:93–99.
    doi: 10.1016/S0168-1702(01)00299-4pubmed: 11597754google scholar: lookup
  21. Rushton J.O., Kolodziejek J., Nell B., Weissenbock H., Nowotny N.. Keratoconjunctivitis in a group of Icelandic horses with suspected gamma-herpesvirus involvement.. Equine Vet. J. 2016;48:427–429.
    doi: 10.1111/evj.12465pubmed: 26032576google scholar: lookup
  22. Borchers K., Ebert M., Fetsch A., Hammond T., Sterner-Kock A.. Prevalence of equine herpesvirus type 2 (EHV-2) DNA in ocular swabs and its cell tropism in equine conjunctiva.. Vet. Microbiol. 2006;118:260–266.
    doi: 10.1016/j.vetmic.2006.07.024pubmed: 16996233google scholar: lookup
  23. Hollingsworth S.R., Pusterla N., Kass P.H., Good K.L., Brault S.A., Maggs D.J.. Detection of equine herpesvirus in horses with idiopathic keratoconjunctivitis and comparison of three sampling techniques.. Vet. Ophthalmol. 2015;18:416–421.
    doi: 10.1111/vop.12250pubmed: 25594353google scholar: lookup
  24. Williams K.J., Maes R., Del Piero F., Lim A., Wise A., Bolin D.C., Caswell J., Jackson C., Robinson N.E., Derksen F.. Equine multinodular pulmonary fibrosis: A newly recognized herpesvirus-associated fibrotic lung disease.. Vet. Pathol. 2007;44:849–862.
    doi: 10.1354/vp.44-6-849pubmed: 18039898google scholar: lookup
  25. Nordengrahn A., Merza M., Ros C., Lindholmc A., Palfl V., Hannant D., Belak S.. Prevalence of equine herpesvirus types 2 and 5 in horse populations by using type-specific PCR assays.. Vet. Res. 2002;33:251–259.
    doi: 10.1051/vetres:2002013pubmed: 12056476google scholar: lookup
  26. Torfason E.G., Thorsteinsdottir L., Torsteinsdottir S., Svansson V.. Study of equid herpesviruses 2 and 5 in Iceland with a type-specific polymerase chain reaction.. Res. Vet. Sci. 2008;85:605–611.
    doi: 10.1016/j.rvsc.2008.01.003pubmed: 18336849google scholar: lookup
  27. 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
  28. Akkutay A.Z., Osterrieder N., Damiani A., Tischer B.K., Borchers K., Alkan F.. Prevalence of equine gammaherpesviruses on breeding farms in Turkey and development of a TaqMan MGB real-time PCR to detect equine herpesvirus 5 (EHV-5). Arch. Virol. 2014;159:2989–2995.
    doi: 10.1007/s00705-014-2165-5pubmed: 25008897google scholar: lookup
  29. Ataseven V.S., Bilge-Dagalp S., Oguzoglu T.C., Karapinar Z., Guzel M., Tan M.T.. Detection and sequence analysis of equine gammaherpesviruses from horses with respiratory tract disease in Turkey.. Transbound. Emerg. Dis. 2010;57:271–276.
  30. Diallo I.S., Hewitson G.R., de Jong A., Kelly M.A., Wright D.J., Corney B.G., Rodwell B.J.. 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
  31. McBrearty K.A., Murray A., Dunowska M.. A survey of respiratory viruses in New Zealand horses.. N. Z. Vet. J. 2013;61:254–261.
    doi: 10.1080/00480169.2012.745211pubmed: 23425354google scholar: lookup
  32. Negussie H., Gizaw D., Tesfaw L., Li Y., Oguma K., Sentsui H., Tessema T.S., Nauwynck H.J.. 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
  33. Back H., Ullman K., Leijon M., Soderlund R., Penell J., Stahl K., Pringle J., Valarcher J.F.. Genetic variation and dynamics of infections of equid herpesvirus 5 in individual horses.. J. Gen. Virol. 2016;97:169–178.
    doi: 10.1099/jgv.0.000332pubmed: 26518010google scholar: lookup
  34. Mekuria Z.H., El-Hage C., Ficorilli N.P., Washington E.A., Gilkerson J.R., Hartley C.A.. Mapping B lymphocytes as major reservoirs of naturally occurring latent equine herpesvirus 5 infection.. J. Gen. Virol. 2017;98:461–470.
    doi: 10.1099/jgv.0.000668pubmed: 27902371google scholar: lookup
  35. Drummer H.E., Reubel G.H., Studdert M.J.. Equine gammaherpesvirus 2 (EHV2) is latent in B lymphocytes.. Arch. Virol. 1996;141:495–504.
    doi: 10.1007/BF01718313pubmed: 8645091google scholar: lookup
  36. Rizvi S.M., Slater J.D., Wolfinger U., Borchers K., Field H.J., Slade A.J.. Detection and distribution of equine herpesvirus 2 DNA in the central and peripheral nervous systems of ponies.. J. Gen. Virol. 1997;78:1115–1118.
    doi: 10.1099/0022-1317-78-5-1115pubmed: 9152431google scholar: lookup
  37. Stasiak K., Dunowska M., Rola J.. Prevalence and sequence analysis of equid herpesviruses from the respiratory tract of Polish horses.. Virol. J. 2018;15:106.
    doi: 10.1186/s12985-018-1018-3pmc: PMC6042439pubmed: 29996858google scholar: lookup
  38. Dunowska M., Wilks C.R., Studdert M.J., Meers J.. Equine respiratory viruses in foals in New Zealand.. N. Z. Vet. J. 2002;50:140–147.
    doi: 10.1080/00480169.2002.36300pubmed: 16032260google scholar: lookup
  39. Murray M.J., Eichorn E.S., Dubovi E.J., Ley W.B., Cavey D.M.. Equine herpesvirus type 2: Prevalence and seroepidemiology in foals.. Equine Vet. J. 1996;28:432–436.
  40. Fornal A., Kowalska K., Zabek T., Piestrzynska-Kajtoch A., Musial A.D., Ropka-Molik K.. Genetic diversity and population structure of polish konik horse based on individuals from all the male founder lines and microsatellite markers.. Animals 2020;10:1569.
    doi: 10.3390/ani10091569pmc: PMC7552212pubmed: 32899310google scholar: lookup
  41. Fu Z.F., Robinson A.J., Horner G.W., Dickinson L.G., Grimmett J.B., Marshall R.B.. Respiratory disease in foals and the epizootiology of equine herpesvirus type 2 infection.. N. Z. Vet. J. 1986;34:152–155.
    doi: 10.1080/00480169.1986.35331pubmed: 16031314google scholar: lookup
  42. Dunowska M., Howe L., Hanlon D., Stevenson M.. Kinetics of equid herpesvirus type 2 infections in a group of thoroughbred foals.. Vet. Microbiol. 2011;152:176–180.
    doi: 10.1016/j.vetmic.2011.04.017pubmed: 21616610google scholar: lookup
  43. Thorsteinsdottir L., Jonsdottir S., Stefansdottir S.B., Andresdottir V., Wagner B., Marti E., Torsteinsdottir S., Svansson V.. The effect of maternal immunity on the equine gammaherpesvirus type 2 and 5 viral load and antibody response.. PLoS ONE 2019;14:e0218576.
  44. Stasiak K., Dunowska M., Trewick S., Rola J.. Genetic variation in the glycoprotein b sequence of equid herpesvirus 5 among horses of various breeds at polish national studs.. Pathogens 2021;10:322.
    doi: 10.3390/pathogens10030322pmc: PMC7998979pubmed: 33803246google scholar: lookup
  45. Muscat K.E., Padalino B., Hartley C.A., Ficorilli N., Celi P., Knight P., Raidal S., Gilkerson J.R., Muscatello G.. Equine transport and changes in equid herpesvirus’ status.. Front. Vet. Sci. 2018;5:224.
    doi: 10.3389/fvets.2018.00224pmc: PMC6167981pubmed: 30320126google scholar: lookup
  46. Costantini D., Seeber P.A., Soilemetzidou S.E., Azab W., Bohner J., Buuveibaatar B., Czirjak G.A., East M.L., Greunz E.M., Kaczensky P.. Physiological costs of infection: Herpesvirus replication is linked to blood oxidative stress in equids.. Sci. Rep. 2018;8:10347.
    doi: 10.1038/s41598-018-28688-0pmc: PMC6037783pubmed: 29985431google scholar: lookup
  47. Lansade L., Foury A., Reigner F., Vidament M., Guettier E., Bouvet G., Soulet D., Parias C., Ruet A., Mach N.. Progressive habituation to separation alleviates the negative effects of weaning in the mother and foal.. Psychoneuroendocrinology 2018;97:59–68.
  48. Henry S., Sigurjonsdottir H., Klapper A., Joubert J., Montier G., Hausberger M.. Domestic foal weaning: Need for re-thinking breeding practices?. Animals 2020;10:361.
    doi: 10.3390/ani10020361pmc: PMC7070483pubmed: 32102206google scholar: lookup

Citations

This article has been cited 2 times.
  1. Stasiak K, Dunowska M, Rola J. Genetic Diversity of Equid Herpesvirus 5 in Temporal Samples from Mares and Their Foals at Three Polish National Studs. Int J Mol Sci 2025 Aug 27;26(17).
    doi: 10.3390/ijms26178298pubmed: 40943220google scholar: lookup
  2. 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 Sep 5;11(9).
    doi: 10.3390/pathogens11091016pubmed: 36145448google scholar: lookup