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Viruses2021; 13(9); doi: 10.3390/v13091686

Prevalence of Nasal Shedding of Equid Gammaherpesviruses in Healthy Swiss Horses.

Abstract: Equid Gamma herpesvirus (eGHV) infections have been reported worldwide and may be correlated with clinical signs, e.g., affecting the respiratory tract in young horses. eGHV are shed by healthy horses as well as horses with respiratory tract disease. The prevalence in healthy Swiss horses is unknown to date but this data would provide valuable information for causal diagnosis in clinical cases and formulation of biosecurity recommendations. Nasal swabs from 68 healthy horses from 12 Swiss stables and 2 stables near the Swiss border region in Germany were analyzed by panherpes nested PCR. Positive samples were sequenced. A multivariable model was used to determine if sex, age, breed, canton, or stable had a significant effect on the shedding status of each detected eGHV. Overall, the eGHV prevalence was 59% (n = 68); the prevalence for equid herpesvirus-2 (EHV-2), equid herpesvirus-5 (EHV-5) and asinine herpesvirus-5 (AHV-5) was 38%, 12% and 9%, respectively. Co-infections with multiple eGHVs were observed in 25% of the positive samples. The odds of shedding EHV-2 decreased with age (p = 0.01) whereas the odds of shedding AHV-5 increased with age (p = 0.04). Breed, sex, canton, or stable had no significant association with eGHV shedding. As EHV-2 shedding was common in healthy horses a positive PCR result must be interpreted with caution regarding the formulation of biosecurity recommendations and causal diagnosis. As EHV-5 and AHV-5 shedding was less common than EHV-2, a positive test result is more likely to be of clinical relevance. Shedding of multiple eGHV complicates the interpretation of positive test results in a horse.
Publication Date: 2021-08-25 PubMed ID: 34578268PubMed Central: PMC8473365DOI: 10.3390/v13091686Google Scholar: Lookup
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  • Journal Article

Summary

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This research explores the prevalence of Equid Gammaherpesviruses (eGHV) in healthy Swiss horses and concludes that a high percentage of them shed this type of virus. The study also investigates the impact of various factors such as sex, age, breed, canton, and stable on this virus shedding.

Objective of the Study

  • The study aims to determine the prevalence of nasal shedding of eGHV in healthy Swiss horses and its correlation with clinical signs, particularly in the young ones. These viruses have been linked to respiratory diseases in horses.

Research Methodology

  • Nasal swabs from 68 healthy horses from 12 Swiss stables and 2 stables near the Swiss border region in Germany were collected and analyzed.
  • The extracted samples were tested using panherpes nested PCR to detect the presence of eGHVs.
  • Positive samples underwent sequencing for in-depth analysis.
  • The researchers employed a multivariable model to ascertain if sex, age, breed, canton, or stable had any significant effect on the shedding status of each detected eGHV.

Research Findings

  • The overall eGHV prevalence found was 59%. The prevalence for equid herpesvirus-2 (EHV-2), equid herpesvirus-5 (EHV-5) and asinine herpesvirus-5 (AHV-5) was 38%, 12% and 9% respectively.
  • Co-infections with multiple eGHVs were observed in 25% of the positive samples.
  • Age was found to be significant in eGHV shedding, with the odds of shedding EHV-2 decreasing with age. On the other hand, the odds of shedding AHV-5 increased with age.
  • No significant associations were found between eGHV shedding and breed, sex, canton, or stable of the horse.

Implications of the Study

  • In light of the common shedding of EHV-2 in healthy horses, it suggests that a positive PCR result must be interpreted cautiously when making biosecurity recommendations and causal diagnoses.
  • As the shedding of EHV-5 and AHV-5 was found to be less common than EHV-2, a positive test result is more likely to be clinically relevant.
  • Shedding of more than one eGHV confuses the interpretation of positive test results in a horse, suggesting the need for a more precise testing and interpretation approach.

Cite This Article

APA
Scheurer L, Bachofen C, Hardmeier I, Lechmann J, Schoster A. (2021). Prevalence of Nasal Shedding of Equid Gammaherpesviruses in Healthy Swiss Horses. Viruses, 13(9). https://doi.org/10.3390/v13091686

Publication

ISSN: 1999-4915
NlmUniqueID: 101509722
Country: Switzerland
Language: English
Volume: 13
Issue: 9

Researcher Affiliations

Scheurer, Laura
  • Klinik für Pferdemedizin, Departement für Pferde, Vetsuisse Fakultät Zürich, Winterthurerstrasse 260, 8057 Zürich, Switzerland.
Bachofen, Claudia
  • Institut für Virologie, Vetsuisse Fakultät Zürich, Winterthurerstrasse 266a, 8057 Zürich, Switzerland.
Hardmeier, Isabelle
  • Klinik für Pferdemedizin, Departement für Pferde, Vetsuisse Fakultät Zürich, Winterthurerstrasse 260, 8057 Zürich, Switzerland.
Lechmann, Julia
  • Institut für Virologie, Vetsuisse Fakultät Zürich, Winterthurerstrasse 266a, 8057 Zürich, Switzerland.
Schoster, Angelika
  • Klinik für Pferdemedizin, Departement für Pferde, Vetsuisse Fakultät Zürich, Winterthurerstrasse 260, 8057 Zürich, Switzerland.

MeSH Terms

  • Animals
  • Antibodies, Viral / blood
  • DNA, Viral / genetics
  • Female
  • Gammaherpesvirinae / isolation & purification
  • Gammaherpesvirinae / physiology
  • Germany / epidemiology
  • Herpesvirus 1, Equid / classification
  • Herpesvirus 1, Equid / genetics
  • Herpesvirus 1, Equid / isolation & purification
  • Herpesvirus 1, Equid / physiology
  • Horse Diseases / epidemiology
  • Horse Diseases / virology
  • Horses
  • Male
  • Nose / virology
  • Respiratory Tract Diseases / epidemiology
  • Respiratory Tract Diseases / veterinary
  • Respiratory Tract Diseases / virology
  • Switzerland / epidemiology
  • Viremia
  • Virus Shedding

Conflict of Interest Statement

The authors report no conflicts of interest in the present work.

References

This article includes 43 references
  1. 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;140:245–258.
    doi: 10.1007/BF01309860pubmed: 7710353google scholar: lookup
  2. Agius CT, Crabb BS, Telford EA, Davison AJ, Studdert MJ. Comparative studies of the structural proteins and glycoproteins of equine herpesviruses 2 and 5.. J. Gen. Virol. 1994;75:2707–2717.
    doi: 10.1099/0022-1317-75-10-2707pubmed: 7931157google scholar: lookup
  3. Negussie H, Gizaw D, Tessema TS, Nauwynck HJ. Equine Herpesvirus-1 Myeloencephalopathy, an Emerging Threat of Working Equids in Ethiopia.. Transbound. Emerg. Dis. 2017;64:389–397.
    doi: 10.1111/tbed.12377pubmed: 26010868google scholar: lookup
  4. Dall Agnol AM, Beuttemmuller EA, Pilz D, Leme RA, Saporiti V, Headley SA, Alfieri AF, Alfieri AA. Detection of Equid gammaherpesvirus 2 and 5 DNA in the upper respiratory tract of asymptomatic horses from Southern Brazil.. Braz. J. Microbiol. 2019;50:875–878.
    doi: 10.1007/s42770-019-00100-7pmc: PMC6863341pubmed: 31187445google scholar: lookup
  5. Pellett PE, Roizman B. The family Herpesviridae: A brief introduction.. 2007. In: Knipe DM, Howley PM, Griffin DE, Lamb RA, Martin MA, Roizman B, Straus SEE, editors. Fields Virology. 5th ed. Lippincott Williams & Wilkins; Philadelphia, PA, USA: pp. 2479–2499.
  6. 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.2018.00224pmc: PMC6167981pubmed: 30320126google scholar: lookup
  7. Rajcani J, Durmanova V. Mechanisms of replication of alpha- and betaherpesviruses and their pathogenesis.. Bratisl Lek Listy 2001;102:505–514.
    pubmed: 11901707
  8. 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
  9. Dunowska M, Wilks CR, Studdert MJ, 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
  10. Borchers K, Wolfinger U, Goltz M, Broll H, Ludwig H. Distribution and relevance of equine herpesvirus type 2 (EHV-2) infections.. Arch. Virol. 1997;142:917–928.
    doi: 10.1007/s007050050128pubmed: 9191857google scholar: lookup
  11. 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
  12. Fortier G, van Erck E, Pronost S, Lekeux P, Thiry E. Equine gammaherpesviruses: Pathogenesis, epidemiology and diagnosis.. Vet. J. 2010;186:148–156.
    doi: 10.1016/j.tvjl.2009.08.017pubmed: 19766026google scholar: lookup
  13. Dunowska M, Meers J, Johnson RD, Wilks CR. Influence of equine herpesvirus type 2 infection on monocyte chemoattractant protein 1 gene transcription in equine blood mononuclear cells.. Res. Vet. Sci. 2001;71:111–113.
    doi: 10.1053/rvsc.2001.0493pubmed: 11883888google scholar: lookup
  14. Williams KJ, Maes R, Del Piero F, Lim A, Wise A, Bolin DC, Caswell J, Jackson C, Robinson NE, 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
  15. Wong DM, Belgrave RL, Williams KJ, Del Piero F, Alcott CJ, Bolin SR, Marr CM, Nolen-Walston R, Myers RK, Wilkins PA. Multinodular pulmonary fibrosis in five horses.. J. Am. Vet. Med. Assoc. 2008;232:898–905.
    doi: 10.2460/javma.232.6.898pubmed: 18341449google scholar: lookup
  16. Scheurer L, Bachofen C, Herteman N, Hilbe M, Wolfer N, Schoster A. A case series highlighting the role of different gamma-herpesviruses in Equine Multinodular Pulmonary Fibrosis.. Schweiz. Arch. Tierheilkd. 2020;162:245–256.
    doi: 10.17236/sat00255pubmed: 32234694google scholar: lookup
  17. Van Cleemput J, Poelaert KCK, Laval K, Nauwynck HJ. Unravelling the first key steps in equine herpesvirus type 5 (EHV5) pathogenesis using ex vivo and in vitro equine models.. Vet. Res. 2019;50:13.
    doi: 10.1186/s13567-019-0630-6pmc: PMC6380010pubmed: 30777128google scholar: lookup
  18. Williams KJ. Gammaherpesviruses and pulmonary fibrosis: Evidence from humans, horses, and rodents.. Vet. Pathol. 2014;51:372–384.
    doi: 10.1177/0300985814521838pubmed: 24569614google scholar: lookup
  19. Gomez De Witte FG, Frank N, Wilkes RP, Novak JM. Association of asinine herpesvirus-5 with pyogranulomatous pneumonia in a mare.. J. Vet. Intern. Med. 2012;26:1064–1068.
  20. Dunowska M, Wilks CR, Studdert MJ, 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
  21. McBrearty KA, 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
  22. Akkutay AZ, Osterrieder N, Damiani A, Tischer BK, 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
  23. 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
  24. 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
  25. Bell SA, Balasuriya UB, Gardner IA, Barry PA, Wilson WD, Ferraro GL, MacLachlan NJ. 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
  26. Nordengrahn A, Merza M, Ros C, Lindholmc A, Palfl V, Hannant D, Belák 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
  27. Marenzoni ML, Coppola G, Maranesi M, Passamonti F, Capelli K, Capomaccio S, Supplizi AV, 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
  28. Schoster A, Scheurer L, Hardmeier I, Bachofen C. Material intended for publication: Prevalence of EHV-1 and -4 antibodies and nasal shedding depending on vaccination status in healthy Swiss horses.. Manuscript in preparation for submission.
  29. VanDevanter DR, Warrener P, Bennett L, Schultz ER, Coulter S, Garber RL, Rose TM. Detection and analysis of diverse herpesviral species by consensus primer PCR.. J. Clin. Microbiol. 1996;34:1666–1671.
  30. Ehlers B, Borchers K, Grund C, Frölich K, Ludwig H, Buhk HJ. Detection of new DNA polymerase genes of known and potentially novel herpesviruses by PCR with degenerate and deoxyinosine-substituted primers.. Virus Genes. 1999;18:211–220.
    doi: 10.1023/A:1008064118057pubmed: 10456789google scholar: lookup
  31. Lechmann J, Bachofen C, Ackermann M. Investigation into the Virome of Swiss Water Buffaloes.. 2016. Institute of Virology, Vetsuisse Faculty, University of Zürich; Zürich, Switzerland: p. 47. CH-8057 Zürich.
  32. 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
  33. Jerele S, Davis E, Mapes S, Pusterla N, Navas González FJ, Iglesias Pastrana C, Abdelfattah EM, McLean A. Survey of Serum Amyloid A and Bacterial and Viral Frequency Using qPCR Levels in Recently Captured Feral Donkeys from Death Valley National Park (California). Animals. 2020;10:1086.
    doi: 10.3390/ani10061086pmc: PMC7341296pubmed: 32585994google scholar: lookup
  34. Rushton JO, Kolodziejek J, Nell B, Nowotny N. Prevalence of asinine herpesvirus type 5 (AsHV-5) infection in clinically normal Lipizzaner horses.. Vet. J. 2014;200:200–203.
    doi: 10.1016/j.tvjl.2013.10.035pubmed: 24709517google scholar: lookup
  35. Kleiboeker SB, Schommer SK, Johnson PJ, Ehlers B, Turnquist SE, Boucher M, Kreeger JM. Association of two newly recognized herpesviruses with interstitial pneumonia in donkeys (Equus asinus). J. Vet. Diagn. Investig. 2002;14:273–280.
    doi: 10.1177/104063870201400401pubmed: 12152805google scholar: lookup
  36. Vengust M, Wen X, Bienzle D. Herpesvirus-associated neurological disease in a donkey.. J. Vet. Diagn. Investig. 2008;20:820–823.
    doi: 10.1177/104063870802000620pubmed: 18987238google scholar: lookup
  37. Back H, Kendall A, Grandón R, Ullman K, Treiberg-Berndtsson L, Ståhl K, Pringle J. Equine multinodular pulmonary fibrosis in association with asinine herpesvirus type 5 and equine herpesvirus type 5: A case report.. Acta Vet. Scand. 2012;54:57.
    doi: 10.1186/1751-0147-54-57pmc: PMC3511884pubmed: 23009194google scholar: lookup
  38. Telford EA, Studdert MJ, Agius CT, Watson MS, Aird HC, Davison AJ. Equine herpesviruses 2 and 5 are gamma-herpesviruses.. Virology. 1993;195:492–499.
    doi: 10.1006/viro.1993.1400pubmed: 8337826google scholar: lookup
  39. Thorsteinsdóttir L, Jónsdóttir S, Stefánsdóttir SB, Andrésdóttir V, Wagner B, Marti E, Torsteinsdóttir 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.
  40. 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.
  41. Pérez-Tris J, Bensch S. Diagnosing genetically diverse avian malarial infections using mixed-sequence analysis and TA-cloning.. Parasitology. 2005;131:15–23.
    doi: 10.1017/S003118200500733Xpubmed: 16038392google scholar: lookup
  42. Marenzoni ML, Passamonti F, Lepri E, Cercone M, Capomaccio S, Cappelli K, Felicetti M, Coppola G, Coletti M, Thiry E. Quantification of Equid herpesvirus 5 DNA in clinical and necropsy specimens collected from a horse with equine multinodular pulmonary fibrosis.. J. Vet. Diagn. Investig. 2011;23:802–806.
    doi: 10.1177/1040638711407890pubmed: 21908328google scholar: lookup
  43. Pusterla N, Magdesian KG, Mapes SM, Zavodovskaya R, Kass PH. Assessment of quantitative polymerase chain reaction for equine herpesvirus-5 in blood, nasal secretions and bronchoalveolar lavage fluid for the laboratory diagnosis of equine multinodular pulmonary fibrosis.. Equine Vet. J. 2017;49:34–38.
    doi: 10.1111/evj.12545pubmed: 26639080google scholar: lookup