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Journal of veterinary internal medicine2018; 32(6); 2099-2104; doi: 10.1111/jvim.15318

Investigation of an experimental infection model of equine coronavirus in adult horses.

Abstract: Equine coronavirus (ECoV) is a recently reported enteric disease of adult horses. Natural infection by ECoV has been reported in adult horses worldwide, whereas experimental infection has only been reported in juvenile horses. An experimental infection model is needed to study the clinical presentation, laboratory abnormalities, and pathophysiological changes associated with ECoV. Objective: To investigate the clinical, hematologic, molecular, and serological features of adult horses experimentally infected with ECoV. Methods: Eight adult horses. Methods: Four horses were intragastrically infected with fecal material containing 10 genome equivalents of ECoV. Four additional horses were exposed daily to the feces from the experimentally-infected horses. Monitoring included physical examinations, as well as daily nasal swab, whole blood, and fecal collection for molecular detection of ECoV. Blood was collected every other day for hematologic analysis and weekly for serologic analysis. Results: All 8 horses shed ECoV in feces. Six of the 8 horses (75%) exhibited mild, clinical disease with soft, formed manure; 1 horse exhibited transient pyrexia. All horses maintained total white cell counts within normal limits, but 3 horses developed transient lymphopenia. No statistically significant differences (P = .20) were observed in quantity of fecal shedding of ECoV between the 2 groups. Conclusions: Experimental infection of adult horses with ECoV was associated with mild and self-limiting clinical signs, transient lymphopenia, and fecal shedding of ECoV, which mimics natural infection. No differences between experimentally-infected horses and horses exposed to ECoV-containing feces were identified. Results of our study support a fecal-oral route of transmission.
Publication Date: 2018-10-24 PubMed ID: 30353949PubMed Central: PMC6271284DOI: 10.1111/jvim.15318Google Scholar: Lookup
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  • Journal Article

Summary

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This research article discusses a study on adult horses experimentally infected with Equine coronavirus (ECoV), establishing that this disease typically causes minor symptoms, temporary lymphopenia, and ECoV shedding in feces, and is likely transmitted via a fecal-oral route.

Research Background

  • The study investigates an experimental infection model of equine coronavirus (ECoV) in adult horses. The coronavirus ECoV primarily impacts adult horses and has been reported worldwide. However, its experimental infection has been predominantly reported in young horses.

Research Objectives and Methods

  • The objective of the research was to investigate clinical, hematologic, molecular, and serological aspects of adult horses experimentally infected with ECoV. To fulfil this purpose, eight adult horses were selected for the experiment.
  • The research model involved intragastrically infecting four horses among the group with fecal matter that contained ten genome equivalents of ECoV. The remaining four were exposed daily to the feces from the experimentally infected horses.
  • Monitoring was done through daily physical exams, nasal swabbing, whole blood collection, and fecal collection for detecting the presence of ECoV. Blood for hematologic analysis was collected on alternate days while a weekly collection of blood was done for serologic analysis.

Research Results

  • All eight horses exhibited ECoV shedding in their feces. Furthermore, six out of eight horses (75%) showed mild clinical signs, including soft, formed manure. One horse experienced transient pyrexia.
  • The total white cell counts remained within normal boundaries for all the horses, even though three developed transient lymphopenia. There was no statistically significant difference observed in the amount of fecal ECoV shedding between the two groups of horses.

Conclusions

  • The conclusions drawn from the study indicate that the experimental infection of adult horses with ECoV corresponds with mild and temporary clinical signs, fleeting lymphopenia, and fecal shedding of ECoV. This closely mirrors natural infection scenarios.
  • There were no discernible differences identified between the horses that were experimentally infected and horses that were exposed to ECoV-containing feces, suggesting that the fecal-oral path is a likely route of transmission.

Cite This Article

APA
Schaefer E, Harms C, Viner M, Barnum S, Pusterla N. (2018). Investigation of an experimental infection model of equine coronavirus in adult horses. J Vet Intern Med, 32(6), 2099-2104. https://doi.org/10.1111/jvim.15318

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 32
Issue: 6
Pages: 2099-2104

Researcher Affiliations

Schaefer, Emily
  • William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis, Davis, California.
Harms, Corey
  • William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis, Davis, California.
Viner, Molly
  • William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis, Davis, California.
Barnum, Samantha
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, Davis, California.
Pusterla, Nicola
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, Davis, California.

MeSH Terms

  • Animals
  • Betacoronavirus 1
  • Coronavirus Infections / pathology
  • Coronavirus Infections / transmission
  • Coronavirus Infections / veterinary
  • Coronavirus Infections / virology
  • Disease Models, Animal
  • Feces / virology
  • Female
  • Horse Diseases / pathology
  • Horse Diseases / transmission
  • Horse Diseases / virology
  • Horses
  • Lymphocyte Count / veterinary
  • Male
  • Real-Time Polymerase Chain Reaction / veterinary
  • Virus Shedding

Grant Funding

  • Boehringer Ingelheim

References

This article includes 14 references
  1. 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 2000 Mar;12(2):153-6.
    pubmed: 10730946doi: 10.1177/104063870001200210google scholar: lookup
  2. Giannitti F, Diab S, Mete A, Stanton JB, Fielding L, Crossley B, Sverlow K, Fish S, Mapes S, Scott L, Pusterla N. Necrotizing Enteritis and Hyperammonemic Encephalopathy Associated With Equine Coronavirus Infection in Equids.. Vet Pathol 2015 Nov;52(6):1148-56.
    pubmed: 25648965doi: 10.1177/0300985814568683google scholar: lookup
  3. Miszczak F, Tesson V, Kin N, Dina J, Balasuriya UB, Pronost S, Vabret A. First detection of equine coronavirus (ECoV) in Europe.. Vet Microbiol 2014 Jun 25;171(1-2):206-9.
  4. Oue Y, Morita Y, Kondo T, Nemoto M. Epidemic of equine coronavirus at Obihiro Racecourse, Hokkaido, Japan in 2012.. J Vet Med Sci 2013;75(9):1261-5.
    pubmed: 23648375doi: 10.1292/jvms.13-0056google scholar: lookup
  5. 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 2015 Jan;29(1):307-10.
    pmc: PMC4858071pubmed: 25319406doi: 10.1111/jvim.12480google scholar: lookup
  6. Guy JS, Breslin JJ, Breuhaus B, Vivrette S, Smith LG. Characterization of a coronavirus isolated from a diarrheic foal.. J Clin Microbiol 2000 Dec;38(12):4523-6.
  7. Zaki AM, van Boheemen S, Bestebroer TM, Osterhaus AD, Fouchier RA. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia.. N Engl J Med 2012 Nov 8;367(19):1814-20.
    pubmed: 23075143doi: 10.1056/nejmoa1211721google scholar: lookup
  8. Pusterla N, Mapes S, Wademan C, White A, Ball R, Sapp K, Burns P, Ormond C, Butterworth K, Bartol J, Magdesian KG. Emerging outbreaks associated with equine coronavirus in adult horses.. Vet Microbiol 2013 Feb 22;162(1):228-31.
  9. Nemoto M, Oue Y, Morita Y, Kanno T, Kinoshita Y, Niwa H, Ueno T, Katayama Y, Bannai H, Tsujimura K, Yamanaka T, Kondo T. Experimental inoculation of equine coronavirus into Japanese draft horses.. Arch Virol 2014 Dec;159(12):3329-34.
    pmc: PMC7087042pubmed: 25139547doi: 10.1007/s00705-014-2205-1google scholar: lookup
  10. 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 2016 Jul;28(4):414-8.
    pubmed: 27216723doi: 10.1177/1040638716649643google scholar: lookup
  11. Pusterla N, Holzenkaempfer N, Mapes S, Kass P. Prevalence of equine coronavirus in nasal secretions from horses with fever and upper respiratory tract infection.. Vet Rec 2015 Sep 19;177(11):289.
    pubmed: 26260064doi: 10.1136/vr.103263google scholar: lookup
  12. Magdesian G, Dwyer RM, Arguedas MG, Diarrhea V. Viral diarrhea. Equine Infectious Diseases 2nd ed. St Louis: Elsevier; 2014:198‐203.
  13. Saif LJ. Bovine respiratory coronavirus.. Vet Clin North Am Food Anim Pract 2010 Jul;26(2):349-64.
    pmc: PMC4094360pubmed: 20619189doi: 10.1016/j.cvfa.2010.04.005google scholar: lookup
  14. Zhang J, Guy JS, Snijder EJ, Denniston DA, Timoney PJ, Balasuriya UB. Genomic characterization of equine coronavirus.. Virology 2007 Dec 5;369(1):92-104.
    pmc: PMC7103287pubmed: 17706262doi: 10.1016/j.virol.2007.06.035google scholar: lookup

Citations

This article has been cited 8 times.
  1. Stummer M, Frisch V, Glitz F, Hinney B, Spergser J, Krücken J, Diekmann I, Dimmel K, Riedel C, Cavalleri JV, Rümenapf T, Joachim A, Lyrakis M, Auer A. Presence of Equine and Bovine Coronaviruses, Endoparasites, and Bacteria in Fecal Samples of Horses with Colic.. Pathogens 2023 Aug 15;12(8).
    doi: 10.3390/pathogens12081043pubmed: 37624003google scholar: lookup
  2. Hepworth-Warren KL, Erwin SJ, Moore CB, Talbot JR, Young KAS, Neault MJ, Haugland JC, Robertson JB, Blikslager AT. Risk factors associated with an outbreak of equine coronavirus at a large farm in North Carolina.. Front Vet Sci 2023;10:1060759.
    doi: 10.3389/fvets.2023.1060759pubmed: 36937023google scholar: lookup
  3. Uzal FA, Arroyo LG, Navarro MA, Gomez DE, Asín J, Henderson E. Bacterial and viral enterocolitis in horses: a review.. J Vet Diagn Invest 2022 May;34(3):354-375.
    doi: 10.1177/10406387211057469pubmed: 34763560google scholar: lookup
  4. Willette JA, Kopper JJ, Kogan CJ, Seguin MA, Schott HC. Effect of season and geographic location in the United States on detection of potential enteric pathogens or toxin genes in horses ≥6-mo-old.. J Vet Diagn Invest 2022 May;34(3):407-411.
    doi: 10.1177/10406387211056054pubmed: 34763559google scholar: lookup
  5. Luethy D, Feldman R, Stefanovski D, Aitken MR. Risk factors for laminitis and nonsurvival in acute colitis: Retrospective study of 85 hospitalized horses (2011-2019).. J Vet Intern Med 2021 Jul;35(4):2019-2025.
    doi: 10.1111/jvim.16147pubmed: 33938584google scholar: lookup
  6. Haake C, Cook S, Pusterla N, Murphy B. Coronavirus Infections in Companion Animals: Virology, Epidemiology, Clinical and Pathologic Features.. Viruses 2020 Sep 13;12(9).
    doi: 10.3390/v12091023pubmed: 32933150google scholar: lookup
  7. Wright S. Highlights of recent clinically relevant papers.. Equine Vet Educ 2019 Mar;31(3):114-115.
    doi: 10.1111/eve.13054pubmed: 32313397google scholar: lookup
  8. 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 2019 Jun;248:95-100.
    doi: 10.1016/j.tvjl.2019.05.001pubmed: 31113572google scholar: lookup