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Pathogens (Basel, Switzerland)2021; 10(4); 423; doi: 10.3390/pathogens10040423

Environmental Detection and Potential Transmission of Equine Herpesviruses.

Abstract: Equine herpesviruses (EHV) are a major health concern for domestic and wild equids and represent one of the most economically important disease agents of horses. Most known EHVs are transmitted directly between individuals as a result of direct exposure to exudates and aerosols. However, accumulating evidence suggests that environmental transmission may play a role including air, water, and fomites. Here, we reviewed studies on environmental stability and transmission of EHVs, which may influence viral dynamics and the use of environmental samples for monitoring EHV shedding.
Publication Date: 2021-04-01 PubMed ID: 33916280PubMed Central: PMC8066653DOI: 10.3390/pathogens10040423Google Scholar: Lookup
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  • Journal Article
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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 study’s main focus is on the potential environmental transmission and detection of equine herpesviruses (EHVs), which are a major threat to both domesticated and wild horses, accounting for a significant economic impact.

Equine Herpesviruses Overview

  • The research discusses Equine herpesviruses (EHVs), which pose a significant health risk to domestic and wild horses. These viruses are among the primary disease agents affecting the horse industry. They are traditionally transmitted directly between animals through exposure to infected exudates and aerosols.

Environmental Transmission of EHVs

  • While most known EHV transmissions occur directly between horses, the authors suggest that environmental factors may also play a part in the transmission. These factors include air, water, and fomites (objects or materials that are likely to carry infection, such as clothes, utensils, and furniture).
  • This mode of transmission suggests that the viruses might have more stability in the environment than previously thought, making the surrounding habitat conductive for their survival and proliferation.

Monitoring EHV Shedding

  • This research discusses how understanding the environmental stability and transmission of EHV can influence viral dynamics. This knowledge could also aid in using environmental samples to monitor EHV shedding among equine populations.
  • EHV shedding is the process by which the virus is expelled from an infected horse and can potentially infect others. By studying the environment where this shedding occurs, it is possible to understand the dynamics of the virus and devise strategies to control its spread.

Economic Impact of EHV

  • The research also highlights that EHVs are economically significant, impacting the horse industry mainly through loss of horses, lowered productivity and the cost of disease control measures. These viruses can cause various conditions in horses, ranging from respiratory diseases to abortion, which can lead to significant economic losses.

Conclusion

  • Overall, this research sheds light on the potential environmental routes and stability of EHV transmission, which could influence its control methods. Further research is required to devise effective strategies for managing the transmission of EHVs in both domestic and wild equine populations.

Cite This Article

APA
Dayaram A, Seeber PA, Greenwood AD. (2021). Environmental Detection and Potential Transmission of Equine Herpesviruses. Pathogens, 10(4), 423. https://doi.org/10.3390/pathogens10040423

Publication

ISSN: 2076-0817
NlmUniqueID: 101596317
Country: Switzerland
Language: English
Volume: 10
Issue: 4
PII: 423

Researcher Affiliations

Dayaram, Anisha
  • Department of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research (IZW), 10315 Berlin, Germany.
  • Institute of Neurophysiology, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany.
Seeber, Peter A
  • Department of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research (IZW), 10315 Berlin, Germany.
  • Limnological Institute, University of Konstanz, 78464 Konstanz, Germany.
Greenwood, Alex D
  • Department of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research (IZW), 10315 Berlin, Germany.
  • Department of Veterinary Medicine, Freie Universität Berlin, 14163 Berlin, Germany.

Grant Funding

  • SAW-2015-IZW-1 440 / Leibniz-Gemeinschaft

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 51 references
  1. Reed SM, Toribio RE. Equine herpesvirus 1 and 4.. Vet Clin North Am Equine Pract 2004 Dec;20(3):631-42.
    doi: 10.1016/j.cveq.2004.09.001pubmed: 15519823google scholar: lookup
  2. Lunn DP, Davis-Poynter N, Flaminio MJ, Horohov DW, Osterrieder K, Pusterla N, Townsend HG. Equine herpesvirus-1 consensus statement.. J Vet Intern Med 2009 May-Jun;23(3):450-61.
  3. van Maanen C. Equine herpesvirus 1 and 4 infections: an update.. Vet Q 2002 Jun;24(2):58-78.
    doi: 10.1080/01652176.2002.9695126pubmed: 12095082google scholar: lookup
  4. Patel JR, Heldens J. Equine herpesviruses 1 (EHV-1) and 4 (EHV-4)--epidemiology, disease and immunoprophylaxis: a brief review.. Vet J 2005 Jul;170(1):14-23.
    doi: 10.1016/j.tvjl.2004.04.018pubmed: 15993786google scholar: lookup
  5. Pascoe RR. The effect of equine coital exanthema on the fertility of mares covered by stallions exhibiting the clinical disease.. Aust Vet J 1981 Mar;57(3):111-4.
  6. Hebia I, Fiéni F, Duchamp G, Destrumelle S, Pellerin JL, Zientara S, Vautherot JF, Bruyas JF. Potential risk of equine herpes virus 1 (EHV-1) transmission by equine embryo transfer.. Theriogenology 2007 Jun;67(9):1485-91.
  7. Azab W, Dayaram A, Greenwood AD, Osterrieder N. How Host Specific Are Herpesviruses? Lessons from Herpesviruses Infecting Wild and Endangered Mammals.. Annu Rev Virol 2018 Sep 29;5(1):53-68.
  8. Abdelgawad A, Azab W, Damiani AM, Baumgartner K, Will H, Osterrieder N, Greenwood AD. Zebra-borne equine herpesvirus type 1 (EHV-1) infection in non-African captive mammals.. Vet Microbiol 2014 Feb 21;169(1-2):102-6.
    doi: 10.1016/j.vetmic.2013.12.011pubmed: 24440374google scholar: lookup
  9. Wohlsein P, Lehmbecker A, Spitzbarth I, Algermissen D, Baumgärtner W, Böer M, Kummrow M, Haas L, Grummer B. Fatal epizootic equine herpesvirus 1 infections in new and unnatural hosts.. Vet Microbiol 2011 May 5;149(3-4):456-60.
    doi: 10.1016/j.vetmic.2010.11.024pubmed: 21167662google scholar: lookup
  10. Foote CE, Love DN, Gilkerson JR, Wellington JE, Whalley JM. EHV-1 and EHV-4 infection in vaccinated mares and their foals.. Vet Immunol Immunopathol 2006 May 15;111(1-2):41-6.
    doi: 10.1016/j.vetimm.2006.01.007pubmed: 16513181google scholar: lookup
  11. Pusterla N, Mapes S. Evaluation of an air tester for the sampling of aerosolised equine herpesvirus type 1.. Vet Rec 2008 Sep 6;163(10):306-8.
    doi: 10.1136/vr.163.10.306pubmed: 18776179google scholar: lookup
  12. Goehring LS, Landolt GA, Morley PS. Detection and management of an outbreak of equine herpesvirus type 1 infection and associated neurological disease in a veterinary teaching hospital.. J Vet Intern Med 2010 Sep-Oct;24(5):1176-83.
  13. Saklou NT, Burgess BA, Ashton LV, Morley PS, Goehring LS. Environmental persistence of equid herpesvirus type-1.. Equine Vet J 2021 Mar;53(2):349-355.
    doi: 10.1111/evj.13313pubmed: 32557765google scholar: lookup
  14. Dayaram A, Seeber P, Courtiol A, Soilemetzidou S, Tsangaras K, Franz M, McEwen GK, Azab W, Kaczensky P, Melzheimer J, East ML, Ganbaatar O, Walzer C, Osterrieder N, Greenwood AD. Seasonal host and ecological drivers may promote restricted water as a viral vector.. Sci Total Environ 2021 Jun 15;773:145446.
  15. Seeber PA, Soilemetzidou SE, East ML, Walzer C, Greenwood AD. Equine behavioral enrichment toys as tools for non-invasive recovery of viral and host DNA.. Zoo Biol 2017 Sep;36(5):341-344.
    doi: 10.1002/zoo.21380pubmed: 28901631google scholar: lookup
  16. Ataseven VS, Dağalp BS, Başaran Z, Keskin S. Seroepidemiological studies of equine herpesviruses 1 (EHV-1) and 4 (EHV-4) infections in working horses from the eastern Turkey. Vet. Fak. Derg. 2010;50:039–042.
  17. Seeber PA, Dayaram A, Sicks F, Osterrieder N, Franz M, Greenwood AD. Noninvasive Detection of Equid Herpesviruses in Fecal Samples.. Appl Environ Microbiol 2019 Feb 1;85(3).
    doi: 10.1128/AEM.02234-18pmc: PMC6344631pubmed: 30446563google scholar: lookup
  18. Seeber PA, McEwen GK, Löber U, Förster DW, East ML, Melzheimer J, Greenwood AD. Terrestrial mammal surveillance using hybridization capture of environmental DNA from African waterholes.. Mol Ecol Resour 2019 Nov;19(6):1486-1496.
    doi: 10.1111/1755-0998.13069pubmed: 31349392google scholar: lookup
  19. Seeber PA, Quintard B, Sicks F, Dehnhard M, Greenwood AD, Franz M. Environmental stressors may cause equine herpesvirus reactivation in captive Grévy's zebras (Equus grevyi).. PeerJ 2018;6:e5422.
    doi: 10.7717/peerj.5422pmc: PMC6109370pubmed: 30155350google scholar: lookup
  20. Mars MH, de Jong MC, van Maanen C, Hage JJ, van Oirschot JT. Airborne transmission of bovine herpesvirus 1 infections in calves under field conditions.. Vet Microbiol 2000 Sep 15;76(1):1-13.
    doi: 10.1016/S0378-1135(00)00218-2pubmed: 10925036google scholar: lookup
  21. Jackson MM, Lynch P. Guideline for isolation precautions in hospitals, 1996.. Am J Infect Control 1996 Jun;24(3):203-6.
    doi: 10.1016/s0196-6553(96)90015-2pubmed: 8806999google scholar: lookup
  22. DOLL ER, McCOLLUM WH, BRYANS JT, CROWE ME. Effect of physical and chemical environment on the viability of equine rhinopneumonitis virus propagated in hamsters.. Cornell Vet 1959 Jan;49(1):75-81.
    pubmed: 13619295
  23. Eugster AK. Isolation of bovine herpesvirus III from diarrheic feces. Vet. Microbiol. 1979;3:199–204.
  24. Walter J, Balzer HJ, Seeh C, Fey K, Bleul U, Osterrieder N. Venereal shedding of equid herpesvirus-1 (EHV-1) in naturally infected stallions.. J Vet Intern Med 2012 Nov-Dec;26(6):1500-4.
  25. Pavone S, Sforna M, Gialletti R, Prato S, Marenzoni ML, Mandara MT. Extensive myenteric ganglionitis in a case of equine chronic intestinal pseudo-obstruction associated with EHV-1 infection.. J Comp Pathol 2013 May;148(4):289-93.
    doi: 10.1016/j.jcpa.2012.07.004pubmed: 22935089google scholar: lookup
  26. Whitwell KE, Blunden AS. Pathological findings in horses dying during an outbreak of the paralytic form of Equid herpesvirus type 1 (EHV-1) infection.. Equine Vet J 1992 Jan;24(1):13-9.
  27. Del Piero F, Wilkins PA, Timoney PJ, Kadushin J, Vogelbacker H, Lee JW, Berkowitz SJ, La Perle KM. Fatal nonneurological EHV-1 infection in a yearling filly.. Vet Pathol 2000 Nov;37(6):672-6.
    doi: 10.1354/vp.37-6-672pubmed: 11105961google scholar: lookup
  28. Pluháček J, Tučková V, King SR. Overmarking behaviour of zebra males: No scent masking, but a group cohesion function across three species. Behav. Ecol. Sociobiol. 2019;73:1–11.
    doi: 10.1007/s00265-019-2744-2google scholar: lookup
  29. Boyd LE. Time budgets of adult Przewalski horses: Effects of sex, reproductive status and enclosure. Appl. Anim. Behav. Sci. 1988;21:19–39.
  30. Crowell-Davis SL, Houpt KA. Coprophagy by foals: effect of age and possible functions.. Equine Vet J 1985 Jan;17(1):17-9.
  31. Bell SA, Pusterla N, Balasuriya UB, Mapes SM, Nyberg NL, MacLachlan NJ. Isolation of a gammaherpesvirus similar to asinine herpesvirus-2 (AHV-2) from a mule and a survey of mules and donkeys for AHV-2 infection by real-time PCR.. Vet Microbiol 2008 Jul 27;130(1-2):176-83.
    doi: 10.1016/j.vetmic.2007.12.013pubmed: 18280676google scholar: lookup
  32. Steuer P, Südekum KH, Müller DW, Franz R, Kaandorp J, Clauss M, Hummel J. Is there an influence of body mass on digesta mean retention time in herbivores? A comparative study on ungulates.. Comp Biochem Physiol A Mol Integr Physiol 2011 Nov;160(3):355-64.
    doi: 10.1016/j.cbpa.2011.07.005pubmed: 21777685google scholar: lookup
  33. 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 Jul;34(7):1666-71.
  34. Webster Marketon JI, Glaser R. Stress hormones and immune function.. Cell Immunol 2008 Mar-Apr;252(1-2):16-26.
    doi: 10.1016/j.cellimm.2007.09.006pubmed: 18279846google scholar: lookup
  35. Vissani MA, Perglione CO, Zabal O, Alvarez G, Thiry E, Barrandeguy M, Parreño V. Topical Ganciclovir Reduces Viral Excretion in Mares With Equine Coital Exanthema.. J Equine Vet Sci 2020 Nov;94:103199.
    doi: 10.1016/j.jevs.2020.103199pubmed: 33077066google scholar: lookup
  36. Seitz SR, Leon JS, Schwab KJ, Lyon GM, Dowd M, McDaniels M, Abdulhafid G, Fernandez ML, Lindesmith LC, Baric RS, Moe CL. Norovirus infectivity in humans and persistence in water.. Appl Environ Microbiol 2011 Oct;77(19):6884-8.
    doi: 10.1128/AEM.05806-11pmc: PMC3187119pubmed: 21856841google scholar: lookup
  37. Bae J, Schwab KJ. Evaluation of murine norovirus, feline calicivirus, poliovirus, and MS2 as surrogates for human norovirus in a model of viral persistence in surface water and groundwater.. Appl Environ Microbiol 2008 Jan;74(2):477-84.
    doi: 10.1128/AEM.02095-06pmc: PMC2223264pubmed: 18065626google scholar: lookup
  38. Bofill-Mas S, Albinana-Gimenez N, Clemente-Casares P, Hundesa A, Rodriguez-Manzano J, Allard A, Calvo M, Girones R. Quantification and stability of human adenoviruses and polyomavirus JCPyV in wastewater matrices.. Appl Environ Microbiol 2006 Dec;72(12):7894-6.
    doi: 10.1128/AEM.00965-06pmc: PMC1694247pubmed: 17028225google scholar: lookup
  39. Espinosa AC, Mazari-Hiriart M, Espinosa R, Maruri-Avidal L, Méndez E, Arias CF. Infectivity and genome persistence of rotavirus and astrovirus in groundwater and surface water.. Water Res 2008 May;42(10-11):2618-28.
    doi: 10.1016/j.watres.2008.01.018pubmed: 18291437google scholar: lookup
  40. Ewald PW. Transmission modes and the evolution of virulence : With special reference to cholera, influenza, and AIDS.. Hum Nat 1991 Mar;2(1):1-30.
    doi: 10.1007/BF02692179pubmed: 24222188google scholar: lookup
  41. Dayaram A, Franz M, Schattschneider A, Damiani AM, Bischofberger S, Osterrieder N, Greenwood AD. Long term stability and infectivity of herpesviruses in water.. Sci Rep 2017 Apr 21;7:46559.
    doi: 10.1038/srep46559pmc: PMC5399353pubmed: 28429732google scholar: lookup
  42. Garvey M, Lyons R, Hector RD, Walsh C, Arkins S, Cullinane A. Molecular Characterisation of Equine Herpesvirus 1 Isolates from Cases of Abortion, Respiratory and Neurological Disease in Ireland between 1990 and 2017.. Pathogens 2019 Jan 15;8(1).
    doi: 10.3390/pathogens8010007pmc: PMC6471309pubmed: 30650561google scholar: lookup
  43. Abdelgawad A, Damiani A, Ho SY, Strauss G, Szentiks CA, East ML, Osterrieder N, Greenwood AD. Zebra Alphaherpesviruses (EHV-1 and EHV-9): Genetic Diversity, Latency and Co-Infections.. Viruses 2016 Sep 20;8(9).
    doi: 10.3390/v8090262pmc: PMC5035975pubmed: 27657113google scholar: lookup
  44. Stommel C, Hofer H, Grobbel M, East ML. Large mammals in Ruaha National Park, Tanzania, dig for water when water stops flowing and water bacterial load increases. Mamm. Biol. 2016;81:21–30.
  45. Donovan TA, Schrenzel MD, Tucker T, Pessier AP, Bicknese B, Busch MD, Wise AG, Maes R, Kiupel M, McKnight C, Nordhausen RW. Meningoencephalitis in a polar bear caused by equine herpesvirus 9 (EHV-9).. Vet Pathol 2009 Nov;46(6):1138-43.
    doi: 10.1354/vp.09-VP-0007-D-CRpubmed: 19605910google scholar: lookup
  46. Ghanem YM, Fukushi H, Ibrahim ES, Ohya K, Yamaguchi T, Kennedy M. Molecular phylogeny of equine herpesvirus 1 isolates from onager, zebra and Thomson's gazelle.. Arch Virol 2008;153(12):2297-302.
    doi: 10.1007/s00705-008-0247-ypubmed: 19002555google scholar: lookup
  47. Greenwood AD, Tsangaras K, Ho SY, Szentiks CA, Nikolin VM, Ma G, Damiani A, East ML, Lawrenz A, Hofer H, Osterrieder N. A potentially fatal mix of herpes in zoos.. Curr Biol 2012 Sep 25;22(18):1727-31.
    doi: 10.1016/j.cub.2012.07.035pubmed: 22902751google scholar: lookup
  48. Arnemo JM, Ahlqvist P, Andersen R, Berntsen F, Ericsson G, Odden J, Brunberg S, Segerström P, Swenson JE. Risk of capture-related mortality in large free-ranging mammals: Experiences from Scandinavia. Wildl. Biol. 2006;12:109–113.
  49. Dickens MJ, Delehanty DJ, Romero M. Stress: An inevitable component of animal translocation. Biol. Conserv. 2010;143:1329–1341.
  50. 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 Dec 20;118(3-4):260-6.
    doi: 10.1016/j.vetmic.2006.07.024pubmed: 16996233google scholar: lookup
  51. Barnard BJ, Paweska JT. Prevalence of antibodies against some equine viruses in zebra (Zebra burchelli) in the Kruger National Park, 1991-1992.. Onderstepoort J Vet Res 1993 Sep;60(3):175-9.
    pubmed: 7970572

Citations

This article has been cited 4 times.
  1. Pusterla N, Barnum S, Young A, Mendonsa E, Lee S, Hankin S, Brittner S, Finno CJ. Molecular Monitoring of EHV-1 in Silently Infected Performance Horses through Nasal and Environmental Sample Testing.. Pathogens 2022 Jun 24;11(7).
    doi: 10.3390/pathogens11070720pubmed: 35889966google scholar: lookup
  2. Mureşan A, Mureşan C, Siteavu M, Avram E, Bochynska D, Taulescu M. An Outbreak of Equine Herpesvirus-4 in an Ecological Donkey Milk Farm in Romania.. Vaccines (Basel) 2022 Mar 18;10(3).
    doi: 10.3390/vaccines10030468pubmed: 35335100google scholar: lookup
  3. Nielsen SS, Alvarez J, Bicout DJ, Calistri P, Canali E, Drewe JA, Garin-Bastuji B, Gonzales Rojas JL, Gortázar C, Herskin M, Michel V, Miranda Chueca MÁ, Roberts HC, Padalino B, Pasquali P, Spoolder H, Ståhl K, Calvo AV, Viltrop A, Winckler C, Carvelli A, Paillot R, Broglia A, Kohnle L, Baldinelli F, Van der Stede Y. Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): infection with Equine Herpesvirus-1.. EFSA J 2022 Jan;20(1):e07036.
    doi: 10.2903/j.efsa.2022.7036pubmed: 35035581google scholar: lookup
  4. Vissani MA, Damiani AM, Barrandeguy ME. Equine Coital Exanthema: New Insights on the Knowledge and Leading Perspectives for Treatment and Prevention.. Pathogens 2021 Aug 20;10(8).
    doi: 10.3390/pathogens10081055pubmed: 34451519google scholar: lookup