Analyze Diet
The veterinary quarterly2024; 44(1); 1-6; doi: 10.1080/01652176.2023.2288876

Investigation of the seroprevalence to equine coronavirus and SARS-CoV-2 in healthy adult horses recently imported to the United States.

Abstract: Adult horses are susceptible to equine coronavirus (ECoV) and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), although, only ECoV has been linked to clinical disease. Little information is available regarding the seroprevalence against ECoV and SARS-CoV-2 in adult healthy horses. The goal of the present study was to determine the seroprevalence against two coronaviruses known to infect horses using convenience samples collected from horses recently imported from Europe to the United States from 2019 to 2023. A total of 385 banked serum samples were tested against ECoV and SARS-CoV-2 using previously validated ELISA assays. Prevalence factors including date of arrival in the United States, signalment and country of origin were available for the majority of the horses. A total of 9/385 (2.3%) and 4/385 (1.0%) horses tested seropositive for ECoV and SARS-CoV-2, respectively. The ECoV seropositive horses were all mares, ages 4 to 26 years (median 9 years) and originated from Germany, the Netherlands, Ireland, Belgium and Italy. These mares were predominantly imported during the summer and fall months. All SARS-CoV-2 seropositive horses were mares ages 5 to 10 years (median 7.5 years) imported from the Netherlands and the United Kingdom. The majority of the SARS-CoV-2 seropositive horses were imported during the colder months of the year. The study results support the presence of ECoV in Europe and report on the first SARS-CoV-2 seropositive healthy adult horses outside the United States. Commingling for movements by air and close contact to humans may predispose transmission with ECoV and SARS-CoV-2, respectively.
Publication Date: 2024-03-18 PubMed ID: 38010292PubMed Central: PMC10949836DOI: 10.1080/01652176.2023.2288876Google 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.

This research examines the prevalence of both equine coronavirus (ECoV) and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in adult horses that have been recently imported to the United States.

Overview

Adult horses can be infected by both equine coronavirus (ECoV) and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). However, only ECoV has been associated with clinical disease in these animals. The researchers aimed to determine the prevalence of these infections in healthy adult horses that have been recently imported to the United States from Europe.

Method

  • The study was conducted on serum samples obtained from 385 horses imported from Europe to the United States between 2019 and 2023.
  • All samples were tested for signs of infection by both ECoV and SARS-CoV-2 using already validated ELISA testing.
  • Additional factors such as the horse’s date of arrival in the United States, country of origin, and signalment were considered.

Findings

  • Out of the 385 tested horses, 9 (2.3%) were found to be seropositive for ECoV, and 4 (1.0%) for SARS-CoV-2.
  • The ECoV positive horses were exclusively mares ranging from 4 to 26 years old, and they predominantly originated from Germany, the Netherlands, Belgium, Ireland, and Italy. Most of these mares were imported during summer and fall months.
  • All the SARS-CoV-2 positive horses, similarly, were mares but between 5 to 10 years of age and they were imported from the Netherlands and the United Kingdom. Majority of these animals were imported during the colder months.

Conclusion

The findings from this study corroborate the presence of ECoV in Europe. It is also the first study to report SARS-CoV-2 in healthy adult horses outside of the United States. The researchers suggest that transmission of these viruses may occur due to close contact with humans and horse commingling during air transport.

Cite This Article

APA
Pusterla N, Lawton K, Barnum S. (2024). Investigation of the seroprevalence to equine coronavirus and SARS-CoV-2 in healthy adult horses recently imported to the United States. Vet Q, 44(1), 1-6. https://doi.org/10.1080/01652176.2023.2288876

Publication

ISSN: 1875-5941
NlmUniqueID: 7909485
Country: England
Language: English
Volume: 44
Issue: 1
Pages: 1-6

Researcher Affiliations

Pusterla, Nicola
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Lawton, Kaila
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Barnum, Samantha
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, CA, USA.

MeSH Terms

  • Humans
  • Horses
  • Animals
  • Female
  • United States / epidemiology
  • Betacoronavirus 1
  • SARS-CoV-2
  • Seroepidemiologic Studies
  • Horse Diseases / epidemiology
  • COVID-19 / epidemiology
  • COVID-19 / veterinary

Conflict of Interest Statement

No potential conflict of interest was reported by the authors.

References

This article includes 35 references
  1. Berryhill EH, Magdesian KG, Aleman M, Pusterla N. Clinical presentation, diagnostic findings, and outcome of adult horses with equine coronavirus infection at a veterinary teaching hospital: 33 cases (2012–2018).. Vet J 248:95–100.
    doi: 10.1016/j.tvjl.2019.05.001pmc: PMC7110482pubmed: 31113572google scholar: lookup
  2. Bosco-Lauth AM, Walker A, Guilbert L, Porter S, Hartwig A, McVicker E, Bielefeldt-Ohmann H, Bowen RA. Susceptibility of livestock to SARS-CoV-2 infection.. Emerg Microbes Infect 10(1):2199–2201.
  3. Bryan J, Marr CM, Mackenzie CJ, Mair TS, Fletcher A, Cash R, Phillips M, Pusterla N, Mapes S, Foote AK. Detection of equine coronavirus in horses in the United Kingdom.. Vet Rec 184(4):123–123.
    doi: 10.1136/vr.105098pubmed: 30530800google scholar: lookup
  4. Davis E, Rush BR, Cox J, DeBey B, Kapil S. Neonatal enterocolitis associated with coronavirus infection in a foal: a case report.. J Vet Diagn Invest 12(2):153–156.
    doi: 10.1177/104063870001200210pubmed: 10730946google scholar: lookup
  5. Decaro N, Grassi A, Lorusso E, Patterson EI, Lorusso A, Desario C, Anderson ER, Vasinioti V, Wastika CE, Hughes GL. Long-term persistence of neutralizing SARS-CoV-2 antibodies in pets.. Transbound Emerg Dis 69(5):3073–3076.
    doi: 10.1111/tbed.14308pmc: PMC8662060pubmed: 34469620google scholar: lookup
  6. Deng J, Jin Y, Liu Y, Sun J, Hao L, Bai J, Huang T, Lin D, Jin Y, Tian K. Serological survey of SARS-CoV-2 for experimental, domestic, companion and wild animals excludes intermediate hosts of 35 different species of animals.. Transbound Emerg Dis 67(4):1745–1749.
    doi: 10.1111/tbed.13577pmc: PMC7264586pubmed: 32303108google scholar: lookup
  7. Dominguez M, Münstermann S, de Guindos I, Timoney P. Equine disease events resulting from international horse movements: systematic review and lessons learned.. Equine Vet J 48(5):641–653.
    doi: 10.1111/evj.12523pubmed: 26509734google scholar: lookup
  8. Englund L, Pringle J. New diseases and increased risk of diseases in companion animals and horses due to transport.. Acta Vet Scand Suppl 100:19–25.
    pubmed: 16429803
  9. Felici M, Cogger N, Riley CB, Padalino B. Pilot study on annual horse movements by air and the possible effect of the Covid-19 pandemic.. J Equine Vet Sci 121:104208.
    doi: 10.1016/j.jevs.2022.104208pubmed: 36596349google scholar: lookup
  10. Fielding CL, Higgins JK, Higgins JC, McIntosh S, Scott E, Giannitti F, Mete A, Pusterla N. Disease associated with equine coronavirus infection and high case fatality rate.. J Vet Intern Med 29(1):307–310.
    doi: 10.1111/jvim.12480pmc: PMC4858071pubmed: 25319406google scholar: lookup
  11. Giannitti F, Diab S, Mete A, Stanton JB, Fielding L, Crossley B, Sverlow K, Fish S, Mapes S, Scott L. Necrotizing enteritis and hyperammonemic encephalopathy associated with equine coronavirus infection in equids.. Vet Pathol 52(6):1148–1156.
    doi: 10.1177/0300985814568683pubmed: 25648965google scholar: lookup
  12. Guy JS, Breslin JJ, Breuhaus B, Vivrette S, Smith LG. Characterization of a coronavirus isolated from a diarrheic foal.. J Clin Microbiol 38(12):4523–4526.
  13. Hierweger MM, Remy-Wohlfender F, Franzen J, Koch MC, Blau D, Schoster A, Nicholson P, Gerber V, Gurtner C, Fouché N. Outbreak of equine coronavirus disease in adult horses, Switzerland 2021.. Transbound Emerg Dis 69(4):1691–1694.
    doi: 10.1111/tbed.14501pubmed: 35243797google scholar: lookup
  14. Kambayashi Y, Bannai H, Tsujimura K, Hirama A, Ohta M, Nemoto M. Outbreak of equine coronavirus infection among riding horses in Tokyo, Japan.. Comp Immunol Microbiol Infect Dis 77:101668.
    doi: 10.1016/j.cimid.2021.101668pubmed: 34004508google scholar: lookup
  15. Kambayashi Y, Nemoto M, Tsujimura K, Ohta M, Bannai H. Serosurveillance of equine coronavirus infection among Thoroughbreds in Japan.. Equine Vet J 55(3):481–486.
    doi: 10.1111/evj.13857pubmed: 35822940google scholar: lookup
  16. Kannan S, Shaik Syed Ali P, Sheeza A. Omicron (B.1.1.529) - variant of concern - molecular profile and epidemiology: a mini review.. Eur Rev Med Pharmacol Sci 25(24):8019–8022.
    doi: 10.26355/eurrev_202112_27653pubmed: 34982466google scholar: lookup
  17. Kooijman LJ, James K, Mapes SM, Theelen MJ, Pusterla N. Seroprevalence and risk factors for infection with equine coronavirus in healthy horses in the USA.. Vet J 220:91–94.
    doi: 10.1016/j.tvjl.2017.01.007pmc: PMC7110631pubmed: 28190504google scholar: lookup
  18. Kooijman LJ, Mapes SM, Pusterla N. Development of an equine coronavirus-specific enzyme-linked immunosorbent assay to determine serologic responses in naturally infected horses.. J Vet Diagn Invest 28(4):414–418.
    doi: 10.1177/1040638716649643pubmed: 27216723google scholar: lookup
  19. Lawton K, Keller SM, Barnum S, Arredondo-Lopez C, Spann K, Pusterla N. Seroprevalence of SARS-CoV-2 in 1186 equids presented to a veterinary medical teaching hospital in California from 2020 to 2022.. Viruses 14(11):2497.
    doi: 10.3390/v14112497pmc: PMC9696554pubmed: 36423106google scholar: lookup
  20. Lawton KOY, Arthur RM, Moeller BC, Barnum S, Pusterla N. Investigation of the role of healthy and sick equids in the COVID-19 pandemic through serological and molecular testing.. Animals 12(5):614.
    doi: 10.3390/ani12050614pmc: PMC8909032pubmed: 35268183google scholar: lookup
  21. Liu Y, Hu G, Wang Y, Ren W, Zhao X, Ji F, Zhu Y, Feng F, Gong M, Ju X. Functional and genetic analysis of viral receptor ACE2 orthologs reveals a broad potential host range of SARS-CoV-2.. Proc Natl Acad Sci USA 118(12):e2025373118.
    doi: 10.1073/pnas.2025373118pmc: PMC8000431pubmed: 33658332google scholar: lookup
  22. Long QX, Tang XJ, Shi QL, Li Q, Deng HJ, Yuan J, Hu JL, Xu W, Zhang Y, Lv FJ. Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections.. Nat Med 26(8):1200–1204.
    doi: 10.1038/s41591-020-0965-6pubmed: 32555424google scholar: lookup
  23. Miszczak F, Tesson V, Kin N, Dina J, Balasuriya UB, Pronost S, Vabret A. First detection of equine coronavirus (ECoV) in Europe.. Vet Microbiol 171(1–2):206–209.
  24. 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 5:224.
    doi: 10.3389/fvets.2018.00224pmc: PMC6167981pubmed: 30320126google scholar: lookup
  25. Nemoto M, Oue Y, Morita Y, Kanno T, Kinoshita Y, Niwa H, Ueno T, Katayama Y, Bannai H, Tsujimura K. Experimental inoculation of equine coronavirus into Japanese draft horses.. Arch Virol 159(12):3329–3334.
    doi: 10.1007/s00705-014-2205-1pmc: PMC7087042pubmed: 25139547google scholar: lookup
  26. Nemoto M, Schofield W, Cullinane A. The first detection of equine coronavirus in adult horses and foals in Ireland.. Viruses 11(10):946.
    doi: 10.3390/v11100946pmc: PMC6832964pubmed: 31615132google scholar: lookup
  27. Oue Y, Ishihara R, Edamatsu H, Morita Y, Yoshida M, Yoshima M, Hatama S, Murakami K, Kanno T. Isolation of an equine coronavirus from adult horses with pyrogenic and enteric disease and its antigenic and genomic characterization in comparison with the NC99 strain.. Vet Microbiol 150(1–2):41–48.
  28. Oue Y, Morita Y, Kondo T, Nemoto M. Epidemic of equine coronavirus at Obihiro Racecourse, Hokkaido, Japan in 2012.. J Vet Med Sci 75(9):1261–1265.
    doi: 10.1292/jvms.13-0056pubmed: 23648375google scholar: lookup
  29. Pusterla N, Chaillon A, Ignacio C, Smith DM, Barnum S, Lawton KOY, Smith G, Pickering B. SARS-CoV-2 seroconversion in an adult horse with direct contact to a COVID-19 individual.. Viruses 14(5):1047.
    doi: 10.3390/v14051047pmc: PMC9145940pubmed: 35632788google scholar: lookup
  30. Pusterla N, Mapes S, Wademan C, White A, Ball R, Sapp K, Burns P, Ormond C, Butterworth K, Bartol J. Emerging outbreaks associated with equine coronavirus in adult horses.. Vet Microbiol 162(1):228–231.
  31. Sack A, Oladunni FS, Gonchigoo B, Chambers TM, Gray GC. Zoonotic diseases from horses: a systematic review.. Vector Borne Zoonotic Dis 20(7):484–495.
    doi: 10.1089/vbz.2019.2541pmc: PMC7339018pubmed: 32077811google scholar: lookup
  32. Schaefer E, Harms C, Viner M, Barnum S, Pusterla N. Investigation of an experimental infection model of equine coronavirus in adult horses.. J Vet Intern Med 32(6):2099–2104.
    doi: 10.1111/jvim.15318pmc: PMC6271284pubmed: 30353949google scholar: lookup
  33. Schvartz G, Tirosh-Levy S, Barnum S, David D, Sol A, Pusterla N, Steinman A. Seroprevalence and risk factors for exposure to equine coronavirus in apparently healthy horses in Israel.. Animals 11(3):894.
    doi: 10.3390/ani11030894pmc: PMC8004030pubmed: 33800990google scholar: lookup
  34. Tråvén M, Näslund K, Linde N, Linde B, Silván A, Fossum C, Hedlund KO, Larsson B. Experimental reproduction of winter dysentery in lactating cows using BCV - comparison with BCV infection in milk-fed calves.. Vet Microbiol 81(2):127–151.
  35. Villanueva-Saz S, Martínez M, Rueda P, Bolea S, Pérez MD, Verde M, Yzuel A, Hurtado-Guerrero R, Pardo J, Santiago L. The dynamics of neutralizing antibodies against SARS-CoV-2 in cats naturally exposed to virus reveals an increase in antibody activity after re-infection.. Vet Res Commun 47(4):2179–2184.
    doi: 10.1007/s11259-023-10087-0pmc: PMC10014409pubmed: 36918467google scholar: lookup