Analyze Diet
Viruses2025; 17(8); 1076; doi: 10.3390/v17081076

Pegiviruses and Coronavirus: Biomolecular Prevalence and Phylogenetic Analysis of Strains Detected in Italian Horse Populations.

Abstract: Equestrian sports play a significant economic role in the horse industry. In recent years, numerous equine viruses have emerged, among which are equine Pegiviruses and the re-emerging Equine coronavirus (ECoV). These viruses are distributed globally and primarily cause subclinical infections with unknown morbidity, even if ECoV can occasionally induce febrile and diarrheic episodes. To broaden the data on the Italian equine population, a study was conducted to assess their prevalence in two distinct horse populations belonging to the Carabinieri Corps (CC) and the Italian Army (IA) of the Italian Armed Forces (IAF). Samples consisted of blood serum and rectal swabs of 436 horses collected within the national surveillance program for equine infectious anemia and gastrointestinal parasite monitoring and analyzed for ( and ) and ECoV by Real-Time RT PCR. The prevalence detected were 6.56% and 3.53%, respectively, for and for the IA, while for the CC, they were 10.13% and 0.84%. Only one sample tested positive for belonging to a horse of the CC. Phylogenetic analyses were carried out on the PCR-positive samples that were sequenced using Sanger protocols. Understanding the epidemiology of these viruses is essential for evaluating the implementation of effective prevention strategies.
Publication Date: 2025-08-02 PubMed ID: 40872790PubMed Central: PMC12390707DOI: 10.3390/v17081076Google 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.

Overview

  • This study investigates the prevalence and genetic relationships of equine Pegiviruses and Equine coronavirus (ECoV) in two distinct populations of horses within the Italian Armed Forces.
  • It provides insight into the distribution of these viruses among Italian horses, aiming to inform better disease control and prevention strategies.

Background and Importance

  • Equestrian sports and horse-related industries have considerable economic importance globally, including Italy.
  • Equine viruses such as Pegiviruses and Equine coronavirus (ECoV) have emerged or re-emerged, raising concerns for horse health.
  • Both viruses are typically associated with subclinical infections (infections without obvious symptoms), making their prevalence and impact difficult to assess.
  • ECoV can sometimes cause clinical symptoms such as fever and diarrhea, although it is not well understood how often or severe these cases might be.

Research Objectives

  • To determine the prevalence of equine Pegiviruses and ECoV in two Italian horse populations: the Carabinieri Corps (CC) and the Italian Army (IA).
  • To perform phylogenetic analyses on viral strains detected, helping to understand the genetic relationships and possible origins.
  • To contribute to epidemiological knowledge that could enhance prevention and control measures for these viral infections in horses.

Methodology

  • Sample Collection:
    • Blood serum and rectal swabs collected from 436 horses during ongoing national surveillance programs.
    • Animals were part of two groups: horses from the Carabinieri Corps (CC) and the Italian Army (IA).
  • Testing Procedures:
    • Real-Time Reverse Transcription Polymerase Chain Reaction (RT-PCR) was used to detect the presence of equine Pegiviruses and ECoV in collected samples.
  • Phylogenetic Analysis:
    • PCR-positive samples were sequenced using Sanger sequencing protocols.
    • The sequences were analyzed to determine the viruses’ evolutionary relationships and genetic diversity.

Results

  • Prevalence of Pegivirus and ECoV in Italian Army Horses (IA):
    • Pegivirus prevalence: 6.56%
    • ECoV prevalence: 3.53%
  • Prevalence of Pegivirus and ECoV in Carabinieri Corps Horses (CC):
    • Pegivirus prevalence: 10.13%
    • ECoV prevalence: 0.84%
  • Only one sample from CC tested positive for a specific Pegivirus strain ( , details not specified in the abstract).
  • Phylogenetic analysis confirmed the presence of genetically distinct viral strains, helping to categorize circulating viruses in these populations.

Conclusions and Implications

  • The study provides important baseline data about the circulation of Pegiviruses and ECoV in Italian military horses.
  • Differences in prevalence between the two horse populations suggest possible variability in exposure or susceptibility that needs further investigation.
  • Since most infections are subclinical, ongoing surveillance is crucial for early detection and management of potential outbreaks.
  • Phylogenetic analysis aids in understanding viral diversity and transmission dynamics, which is vital for developing targeted preventive strategies.
  • Overall, this research underlines the importance of molecular surveillance in maintaining equine health and supporting the equestrian industry’s economic stability.

Cite This Article

APA
(2025). Pegiviruses and Coronavirus: Biomolecular Prevalence and Phylogenetic Analysis of Strains Detected in Italian Horse Populations. Viruses, 17(8), 1076. https://doi.org/10.3390/v17081076

Publication

ISSN: 1999-4915
NlmUniqueID: 101509722
Country: Switzerland
Language: English
Volume: 17
Issue: 8
PII: 1076

Researcher Affiliations

MeSH Terms

  • Animals
  • Horses / virology
  • Italy / epidemiology
  • Phylogeny
  • Horse Diseases / virology
  • Horse Diseases / epidemiology
  • Prevalence
  • Coronavirus / genetics
  • Coronavirus / classification
  • Coronavirus / isolation & purification
  • Coronavirus Infections / veterinary
  • Coronavirus Infections / epidemiology
  • Coronavirus Infections / virology
  • Flaviviridae / genetics
  • Flaviviridae / classification
  • Flaviviridae / isolation & purification
  • Flaviviridae Infections / veterinary
  • Flaviviridae Infections / epidemiology
  • Flaviviridae Infections / virology
  • RNA, Viral / genetics

Grant Funding

  • RC IZSLT09/20 / MINISTRY OF HEALTH

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 90 references
  1. Williams J, Marlin D. Foreword—Emerging issues in equestrian practice.. Comp. Exerc. Physiol. 2020;16:1–4.
    doi: 10.3920/CEP20x001google scholar: lookup
  2. Paillot R. Special issue “equine Viruses”: Old “friends” and new foes?. Viruses 2020;12:153.
    doi: 10.3390/v12020153pmc: PMC7077308pubmed: 32013127google scholar: lookup
  3. Smith BL, Jones JH, Hornof WJ, Miles JA, Longworth KE, Willits NH. Effects of road transport on indices of stress in horses.. Equine Vet. J. 1996;28:446–454.
  4. Grandin T. Assessment of Stress during Handling and Transport.. J. Anim. Sci. 1997;75:249–257.
    doi: 10.2527/1997.751249xpubmed: 9027573google scholar: lookup
  5. Schmidt A, Biau S, Möstl E, Becker-Birck M, Morillon B, Aurich J, Faure JM, Aurich C. Changes in cortisol release and heart rate variability in sport horses during long-distance road transport.. Domest. Anim. Endocrinol. 2010;38:179–189.
  6. Reichert C, Campe A, Walter S, Pfaender S, Welsch K, Ruddat I, Sieme H, Feige K, Steinmann E, Cavalleri JMV. Frequent occurrence of nonprimate hepacivirus infections in Thoroughbred breeding horses—A cross-sectional study for the occurrence of infections and potential risk factors.. Vet. Microbiol. 2017;203:315–322.
    doi: 10.1016/j.vetmic.2017.03.030pubmed: 28619163google scholar: lookup
  7. Timoney PJ. Factors influencing the international spread of equine diseases.. Vet. Clin. N. Am. Equine Pract. 2000;16:537–551.
    doi: 10.1016/S0749-0739(17)30094-9pubmed: 11219348google scholar: lookup
  8. Spence KL, O’Sullivan TL, Poljak Z, Greer AL. Descriptive and network analyses of the equine contact network at an equestrian show in Ontario, Canada and implications for disease spread.. BMC Vet. Res. 2017;13:191.
    doi: 10.1186/s12917-017-1103-7pmc: PMC5480143pubmed: 28637457google scholar: lookup
  9. Dominguez M, Mapitse NJ, Akerström G, Devolz R, Mcewen J, Stewart B, Lam K. The HHP Framework, for Certified High-Health-Status Equine Athlete.. Bulletin De L’OMSA OIE; Paris, France: 2019. p. 3.
    doi: 10.20506/bull.2019.2.2976google scholar: lookup
  10. Chambers TM. A brief introduction to equine influenza and equine influenza viruses.. Methods Mol. Biol. 2020;2123:355–360.
    doi: 10.1007/978-1-0716-0346-8_26pubmed: 32170701google scholar: lookup
  11. Whitlock F, Murcia PR, Newton JR. A Review on Equine Influenza from a Human Influenza Perspective.. Viruses 2022;14:1312.
    doi: 10.3390/v14061312pmc: PMC9229935pubmed: 35746783google scholar: lookup
  12. Davis E, Rush BR, Cox J, DeBey B, Kapil S. Neonatal enterocolitis associated with coronavirus infection in a foal: A case report.. J. Vet. Diagnostic Investig. 2000;12:153–156.
    doi: 10.1177/104063870001200210pubmed: 10730946google scholar: lookup
  13. Guy JS, Breslin JJ, Breuhaus B, Vivrette S, Smith LG. Characterization of a coronavirus isolated from a diarrheic foal.. J. Clin. Microbiol. 2000;38:4523–4526.
  14. Burbelo PD, Dubovi EJ, Simmonds P, Medina JL, Henriquez JA, Mishra N, Wagner J, Tokarz R, Cullen JM, Iadarola MJ. Serology-Enabled Discovery of Genetically Diverse Hepaciviruses in a New Host.. J. Virol. 2012;86:6171–6178.
    doi: 10.1128/JVI.00250-12pmc: PMC3372197pubmed: 22491452google scholar: lookup
  15. Kapoor A, Simmonds P, Cullen JM, Scheel TKH, Medina JL, Giannitti F, Nishiuchi E, Brock KV, Burbelo PD, Rice CM. Identification of a Pegivirus (GB Virus-Like Virus) That Infects Horses.. J. Virol. 2013;87:7185–7190.
    doi: 10.1128/JVI.00324-13pmc: PMC3676142pubmed: 23596285google scholar: lookup
  16. Chandriani S, Skewes-Cox P, Zhong W, Ganem D.E, Divers T.J, Van Blaricum A.J, Tennant B.C, Kistler A.L. Identification of a previously undescribed divergent virus from the Flaviviridae family in an outbreak of equine serum hepatitis.. Proc. Natl. Acad. Sci. USA 2013;110:E1407–E1415.
    doi: 10.1073/pnas.1219217110pmc: PMC3625295pubmed: 23509292google scholar: lookup
  17. Postler T.S, Beer M, Blitvich B.J, Bukh J, de Lamballerie X, Drexler J.F, Imrie A, Kapoor A, Karganova G.G, Lemey P. Renaming of the genus Flavivirus to Orthoflavivirus and extension of binomial species names within the family Flaviviridae.. Arch. Virol. 2023;168:224.
    doi: 10.1007/s00705-023-05835-1pubmed: 37561168google scholar: lookup
  18. Divers T.J, Tennant B.C, Kumar A, McDonough S, Cullen J, Bhuva N, Jain K, Chauhan L.S, Scheel T.K.H, Lipkin W.I. New parvovirus associated with serum hepatitis in horses after inoculation of common biological product.. Emerg. Infect. Dis. 2018;24:303–310.
    doi: 10.3201/eid2402.171031pmc: PMC5782890pubmed: 29350162google scholar: lookup
  19. Rasche A, Lehmann F, Goldmann N, Nagel M, Moreira-Soto A, Nobach D, de Oliveira Carneiro I, Osterrieder N, Greenwood A.D, Steinmann E. A hepatitis B virus causes chronic infections in equids worldwide.. Proc. Natl. Acad. Sci. USA 2021;118:e2013982118.
    doi: 10.1073/pnas.2013982118pmc: PMC8020657pubmed: 33723007google scholar: lookup
  20. Uprety T, Sreenivasan C.C, Hause B.M, Li G, Odemuyiwa S.O, Locke S, Morgan J, Zeng L, Gilsenan W.F, Slovis N. Identification of a ruminant origin group b rotavirus associated with diarrhea outbreaks in foals.. Viruses 2021;13:1330.
    doi: 10.3390/v13071330pmc: PMC8310321pubmed: 34372536google scholar: lookup
  21. Simmonds P, Becher P, Bukh J, Gould E.A, Meyers G, Monath T, Muerhoff S, Pletnev A, Rico-Hesse R, Smith D.B. ICTV virus taxonomy profile: Flaviviridae.. J. Gen. Virol. 2017;98:2–3.
    doi: 10.1099/jgv.0.000672pmc: PMC5370391pubmed: 28218572google scholar: lookup
  22. Tomlinson J.E, Wolfisberg R, Fahnøe U, Sharma H, Renshaw R.W, Nielsen L, Nishiuchi E, Holm C, Dubovi E, Rosenberg B.R. Equine pegiviruses cause persistent infection of bone marrow and are not associated with hepatitis.. PLoS Pathog. 2020;16:e1008677.
  23. Yu Y, Wan Z, Wang J.H, Yang X, Zhang C. Review of human pegivirus: Prevalence, transmission, pathogenesis, and clinical implication.. Virulence 2022;13:324–341.
  24. Sibley S.D, Lauck M, Bailey A.L, Hyeroba D, Tumukunde A, Weny G, Chapman C.A, O’Connor D.H, Goldberg T.L, Friedrich T.C. Discovery and characterization of distinct simian pegiviruses in three wild African old world monkey species.. PLoS ONE 2014;9:e98569.
  25. Porter A.F, Pettersson J.H.O, Chang W.S, Harvey E, Rose K, Shi M, Eden J.S, Buchmann J, Moritz C, Holmes E.C. Novel hepaci- And pegi-like viruses in native Australian wildlife and non-human primates.. Virus Evol. 2020;6:veaa064.
    doi: 10.1093/ve/veaa064pmc: PMC7673076pubmed: 33240526google scholar: lookup
  26. Heffron A.S, Lauck M, Somsen E.D, Townsend E.C, Bailey A.L, Sosa M, Eickhoff J, Capuano S, Newman C.M, Kuhn J.H. Discovery of a novel simian pegivirus in common marmosets (Callithrix jacchus) with lymphocytic enterocolitis.. Microorganisms 2020;8:1509.
  27. Quan P.L, Firth C, Conte J.M, Williams S.H, Zambrana-Torrelio C.M, Anthony S.J, Ellison J.A, Gilbert A.T, Kuzmin I.V, Niezgoda M. Bats are a major natural reservoir for hepaciviruses and pegiviruses.. Proc. Natl. Acad. Sci. USA 2013;110:8194–8199.
    doi: 10.1073/pnas.1303037110pmc: PMC3657805pubmed: 23610427google scholar: lookup
  28. Van Nguyen D, Van Nguyen C, Bonsall D, Ngo T.T, Carrique-Mas J, Pham A.H, Bryant J.E, Thwaites G, Baker S, Woolhouse M. Detection and characterization of homologues of human hepatitis viruses and pegiviruses in rodents and bats in Vietnam.. Viruses 2018;10:102.
    doi: 10.3390/v10030102pmc: PMC5869495pubmed: 29495551google scholar: lookup
  29. Firth C, Bhat M, Firth M.A, Williams S.H, Frye M.J, Simmonds P, Conte J.M, Ng J, Garcia J, Bhuva N.P. Detection of zoonotic pathogens and characterization of novel viruses carried by commensal Rattus norvegicus in New York city.. mBio 2014;5:e01933-14.
    doi: 10.1128/mBio.01933-14pmc: PMC4205793pubmed: 25316698google scholar: lookup
  30. Kapoor A, Simmonds P, Scheel T.K.H, Hjelle B, Cullen J.M, Burbelo P.D, Chauhan L.V, Duraisamy R, Sanchez Leon M, Jain K. Identification of rodent homologs of hepatitis C virus and pegiviruses.. mBio 2013;4:e00216-13.
    doi: 10.1128/mBio.00216-13pmc: PMC3622934pubmed: 23572554google scholar: lookup
  31. Zhu W, Yang J, Lu S, Huang Y, Jin D, Pu J, Liu L, Li Z, Shi M, Xu J. Novel pegiviruses infecting wild birds and rodents. Virol. Sin. 2022;37:208–214.
    doi: 10.1016/j.virs.2022.01.013pmc: PMC9170927pubmed: 35234631google scholar: lookup
  32. Baechlein C, Grundhoff A, Fischer N, Alawi M, Hoeltig D, Waldmann KH, Becher P. Pegivirus infection in domestic pigs, Germany. Emerg. Infect. Dis. 2016;22:1312–1314.
    doi: 10.3201/eid2207.160024pmc: PMC4918184pubmed: 27314228google scholar: lookup
  33. Nishizawa T, Usui R, Narabu Y, Takahashi M, Murata K, Okamoto H. Identification of a novel pegivirus in pet cats (Felis silvestris catus) in Japan. Virus Res. 2021;301:198452.
  34. Lyons S, Kapoor A, Schneider BS, Wolfe ND, Culshaw G, Corcoran B, Durham AE, Burden F, McGorum BC, Simmonds P. Viraemic frequencies and seroprevalence of non-primate hepacivirus and equine pegiviruses in horses and other mammalian species. J. Gen. Virol. 2014;95:1701–1711.
    doi: 10.1099/vir.0.065094-0pubmed: 24814924google scholar: lookup
  35. De Souza AJS, Malheiros AP, de Sousa ERP, Moreira ACN, Silva AL, das Chagas AAC, Freitas PEB, Gemaque BS, de Figueiredo HF, de Sá LRM. First report of equine Pegivirus in South America, Brazil. Acta Trop. 2015;152:56–59.
  36. Lu G, Sun L, Xu T, He D, Wang Z, Ou S, Jia K, Yuan L, Li S. First description of hepacivirus and pegivirus infection in domestic Horses in China: A study in guangdong province, heilongjiang province and Hong Kong district. PLoS ONE 2016;11:e0155662.
  37. Postel A, Cavalleri JMV, Pfaender S, Walter S, Steinmann E, Fischer N, Feige K, Haas L, Becher P. Frequent presence of hepaci and pegiviruses in commercial equine serum pools. Vet. Microbiol. 2016;182:8–14.
    doi: 10.1016/j.vetmic.2015.10.032pubmed: 26711022google scholar: lookup
  38. Lu G, Fu C, Huang J, Xu H, Wu P, Ping X, Li S. Molecular characterization of a genetically divergent equine pegivirus strain identified in China. Arch. Virol. 2018;163:249–252.
    doi: 10.1007/s00705-017-3602-zpubmed: 29094242google scholar: lookup
  39. Tang W, Zhu N, Wang H, Gao Y, Wan Z, Cai Q, Yu S, Tang S. Identification and genetic characterization of equine Pegivirus in China. J. Gen. Virol. 2018;99:768–776.
    doi: 10.1099/jgv.0.001063pubmed: 29658859google scholar: lookup
  40. Figueiredo AS, de Moraes MVDS, Soares CC, Chalhoub FLL, de Filippis AMB, dos Santos DRL, de Almeida FQ, Godoi TLOS, de Souza AM, Burdman TR. First description of Theiler’s disease-associated virus infection and epidemiological investigation of equine pegivirus and equine hepacivirus coinfection in Brazil. Transbound. Emerg. Dis. 2019;66:1737–1751.
    doi: 10.1111/tbed.13210pubmed: 31017727google scholar: lookup
  41. Rodrigues TCS, Subramaniam K, McCulloch SD, Goldstein JD, Schaefer AM, Fair PA, Reif JS, Bossart GD, Waltzek TB. Genomic characterization of a novel pegivirus species from free-ranging bottlenose dolphins (Tursiops truncatus) in the Indian River Lagoon, Florida. Virus Res. 2019;263:98–101.
  42. Wu Z, Wu Y, Zhang W, Merits A, Simmonds P, Wang M, Jia R, Zhu D, Liu M, Zhao X. The First Nonmammalian Pegivirus Demonstrates Efficient In Vitro Replication and High Lymphotropism. J. Virol. 2020;94:e01150-20.
    doi: 10.1128/JVI.01150-20pmc: PMC7527067pubmed: 32759314google scholar: lookup
  43. Divers TJ, Tomlinson JE, Tennant BC. The history of Theiler’s disease and the search for its aetiology. Vet. J. 2022;287:105878.
    doi: 10.1016/j.tvjl.2022.105878pubmed: 35907440google scholar: lookup
  44. Tomlinson JE, Tennant BC, Struzyna A, Mrad D, Browne N, Whelchel D, Johnson PJ, Jamieson C, Löhr CV, Bildfell R. Viral testing of 10 cases of Theiler’s disease and 37 in-contact horses in the absence of equine biologic product administration: A prospective study (2014–2018). J. Vet. Intern. Med. 2019;33:258–265.
    doi: 10.1111/jvim.15362pmc: PMC6335540pubmed: 30520132google scholar: lookup
  45. Tomlinson JE, Kapoor A, Kumar A, Tennant BC, Laverack MA, Beard L, Delph K, Davis E, Schott H, Lascola K. Viral testing of 18 consecutive cases of equine serum hepatitis: A prospective study (2014–2018). J. Vet. Intern. Med. 2019;33:251–257.
    doi: 10.1111/jvim.15368pmc: PMC6335536pubmed: 30520162google scholar: lookup
  46. Lu G, Huang J, Yang Q, Xu H, Wu P, Fu C, Li S. Identification and genetic characterization of hepacivirus and pegivirus in commercial equine serum products in China. PLoS ONE 2017;12:e0189208.
  47. Altan E, Li Y, Sabino-Santos G Jr, Sawaswong V, Barnum S, Pusterla N, Deng X, Delwart E. Viruses in Horses with Neurologic and Respiratory Diseases. Viruses 2019;11:942.
    doi: 10.3390/v11100942pmc: PMC6832430pubmed: 31614994google scholar: lookup
  48. Paim WP, Weber MN, Cibulski SP, da Silva MS, Puhl DE, Budaszewski RF, Varela APM, Mayer FQ, Canal CW. Characterization of the viral genomes present in commercial batches of horse serum obtained by high-throughput sequencing. Biologicals 2019;61:1–7.
  49. Cavalleri JMV, Korbacska-Kutasi O, Leblond A, Paillot R, Pusterla N, Steinmann E, Tomlinson J. European College of Equine Internal Medicine consensus statement on equine flaviviridae infections in Europe. J. Vet. Intern. Med. 2022;36:1858–1871.
    doi: 10.1111/jvim.16581pmc: PMC9708432pubmed: 36367340google scholar: lookup
  50. Nemoto M, Oue Y, Murakami S, Kanno T, Bannai H, Tsujimura K, Yamanaka T, Kondo T. Complete genome analysis of equine coronavirus isolated in Japan. Arch. Virol. 2015;160:2903–2906.
    doi: 10.1007/s00705-015-2565-1pmc: PMC7086706pubmed: 26271151google scholar: lookup
  51. Pusterla N, Vin R, Leutenegger C, Mittel LD, Divers TJ. Equine coronavirus: An emerging enteric virus of adult horses. Equine Vet. Educ. 2016;28:216–223.
    doi: 10.1111/eve.12453pmc: PMC7163714pubmed: 32313392google scholar: lookup
  52. Woo PCY, De Groot RJ, Haagmans B, Lau SKP, Neuman BW, Perlman S, Sola I, Van Der Hoek L, Wong ACP, Yeh SH. ICTV Virus Taxonomy Profile: Coronaviridae 2023. J. Gen. Virol. 2023;104:001843.
    doi: 10.1099/jgv.0.001843pmc: PMC12135074pubmed: 37097842google scholar: lookup
  53. Franzo G, Drigo M, Legnardi M, Grassi L, Pasotto D, Menandro ML, Cecchinato M, Tucciarone CM. Bovine coronavirus: Variability, evolution, and dispersal patterns of a no longer neglected betacoronavirus. Viruses 2020;12:1285.
    doi: 10.3390/v12111285pmc: PMC7697035pubmed: 33182765google scholar: lookup
  54. Vlasova AN, Saif LJ. Bovine Coronavirus and the Associated Diseases. Front. Vet. Sci. 2021;8:643220.
    doi: 10.3389/fvets.2021.643220pmc: PMC8044316pubmed: 33869323google scholar: lookup
  55. Mora-Díaz JC, Piñeyro PE, Houston E, Zimmerman J, Giménez-Lirola LG. Porcine hemagglutinating encephalomyelitis virus: A review. Front. Vet. Sci. 2019;6:53.
    doi: 10.3389/fvets.2019.00053pmc: PMC6402421pubmed: 30873421google scholar: lookup
  56. Wang Q, Vlasova AN, Kenney SP, Saif LJ. Emerging and re-emerging coronaviruses in pigs. Curr. Opin. Virol. 2019;34:39–49.
  57. Bender SJ, Weiss SR. Pathogenesis of murine coronavirus in the central nervous system. J. Neuroimmune Pharmacol. 2010;5:336–354.
    doi: 10.1007/s11481-010-9202-2pmc: PMC2914825pubmed: 20369302google scholar: lookup
  58. Grabherr S, Ludewig B, Pikor NB. Insights into coronavirus immunity taught by the murine coronavirus. Eur. J. Immunol. 2021;51:1062–1070.
    doi: 10.1002/eji.202048984pmc: PMC8250324pubmed: 33687066google scholar: lookup
  59. Banerjee A, Kulcsar K, Misra V, Frieman M, Mossman K. Bats and coronaviruses. Viruses 2019;11:41.
    doi: 10.3390/v11010041pmc: PMC6356540pubmed: 30634396google scholar: lookup
  60. Tang G, Liu Z, Chen D. Human coronaviruses: Origin, host and receptor. J. Clin. Virol. 2022;155:105246.
    doi: 10.1016/j.jcv.2022.105246pmc: PMC9301904pubmed: 35930858google scholar: lookup
  61. Zhang J, Guy JS, Snijder EJ, Denniston DA, Timoney PJ, Balasuriya UBR. Genomic characterization of equine coronavirus. Virology 2007;369:92–104.
    doi: 10.1016/j.virol.2007.06.035pmc: PMC7103287pubmed: 17706262google scholar: lookup
  62. 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. 2011;150:41–48.
  63. 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. 2013;162:228–231.
  64. Miszczak F, Tesson V, Kin N, Dina J, Balasuriya UBR, Pronost S, Vabret A. First detection of equine coronavirus (ECoV) in Europe. Vet. Microbiol. 2014;171:206–209.
  65. Slovis NM, Elam J, Estrada M, Leutenegger CM. Infectious agents associated with diarrhoea in neonatal foals in central Kentucky: A comprehensive molecular study. Equine Vet. J. 2014;46:311–316.
    doi: 10.1111/evj.12119pmc: PMC7163618pubmed: 23773143google scholar: lookup
  66. Kooijman LJ, James K, Mapes SM, Theelen MJP, Pusterla N. Seroprevalence and risk factors for infection with equine coronavirus in healthy horses in the USA. Vet. J. 2017;220:91–94.
    doi: 10.1016/j.tvjl.2017.01.007pmc: PMC7110631pubmed: 28190504google scholar: lookup
  67. 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. 2019;184:123.
    doi: 10.1136/vr.105098pubmed: 30530800google scholar: lookup
  68. Pusterla N, James K, Mapes S, Bain F. Frequency of molecular detection of equine coronavirus in faeces and nasal secretions in 277 horses with acute onset of fever. Vet. Rec. 2019;184:385.
    doi: 10.1136/vr.104919pubmed: 30850426google scholar: lookup
  69. Sanz MG, Kwon SY, Pusterla N, Gold JR, Bain F, Evermann J. Evaluation of equine coronavirus fecal shedding among hospitalized horses. J. Vet. Intern. Med. 2019;33:918–922.
    doi: 10.1111/jvim.15449pmc: PMC6430884pubmed: 30788861google scholar: lookup
  70. Mattei DN, Kopper JJ, Sanz MG. Equine Coronavirus-Associated Colitis in Horses: A Retrospective Study. J. Equine Vet. Sci. 2020;87:102906.
    doi: 10.1016/j.jevs.2019.102906pmc: PMC7126555pubmed: 32172908google scholar: lookup
  71. 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. 2021;77:101668.
    doi: 10.1016/j.cimid.2021.101668pubmed: 34004508google scholar: lookup
  72. 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 2021;11:894.
    doi: 10.3390/ani11030894pmc: PMC8004030pubmed: 33800990google scholar: lookup
  73. Fouché N, Remy-Wohlfender F, Blau D, Franzen J, Gurtner C, Seuberlich T, Unger L, Gerber V. Characterization of an outbreak of equine coronavirus infection in adult horses in Switzerland. Schweiz. Arch. Tierheilkd. 2022;164:733–739.
    doi: 10.17236/sat00372pubmed: 36193783google scholar: lookup
  74. Pusterla N, Vin R, Leutenegger CM, Mittel LD, Divers TJ. Enteric coronavirus infection in adult horses. Vet. J. 2018;231:13–18.
    doi: 10.1016/j.tvjl.2017.11.004pmc: PMC7110460pubmed: 29429482google scholar: lookup
  75. Berryhill EH, Magdesia 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;248:95–100.
    doi: 10.1016/j.tvjl.2019.05.001pmc: PMC7110482pubmed: 31113572google scholar: lookup
  76. Kambayashi Y, Nemoto M, Tsujimura K, Ohta M, Bannai H. Serosurveillance of equine coronavirus infection among Thoroughbreds in Japan. Equine Vet. J. 2023;55:481–486.
    doi: 10.1111/evj.13857pubmed: 35822940google scholar: lookup
  77. Pusterla N. Equine Coronaviruses. Vet. Clin. N. Am.—Equine Pract. 2023;39:55–71.
    doi: 10.1016/j.cveq.2022.11.008pubmed: 36737293google scholar: lookup
  78. 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;29:307–310.
    doi: 10.1111/jvim.12480pmc: PMC4858071pubmed: 25319406google scholar: lookup
  79. 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. 2015;52:1148–1156.
    doi: 10.1177/0300985814568683pubmed: 25648965google scholar: lookup
  80. 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. 2014;159:3329–3334.
    doi: 10.1007/s00705-014-2205-1pmc: PMC7087042pubmed: 25139547google scholar: lookup
  81. 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. 2018;32:2099–2104.
    doi: 10.1111/jvim.15318pmc: PMC6271284pubmed: 30353949google scholar: lookup
  82. Kambayashi Y, Kishi D, Ueno T, Ohta M, Bannai H, Tsujimura K, Kinoshita Y, Nemoto M. Distribution of equine coronavirus RNA in the intestinal and respiratory tracts of experimentally infected horses.. Arch. Virol. 2022;167:1611–1618.
    doi: 10.1007/s00705-022-05488-6pmc: PMC9152306pubmed: 35639190google scholar: lookup
  83. 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;177:289.
    doi: 10.1136/vr.103263pubmed: 26260064google scholar: lookup
  84. 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.2023.1060759pmc: PMC10020641pubmed: 36937023google scholar: lookup
  85. Drzewnioková P, Festa F, Panzarin V, Lelli D, Moreno A, Zecchin B, De Benedictis P, Leopardi S. Best molecular tools to investigate coronavirus diversity in mammals: A comparison.. Viruses 2021;13:1975.
    doi: 10.3390/v13101975pmc: PMC8538982pubmed: 34696405google scholar: lookup
  86. Rausch T, Fritz MHY, Untergasser A, Benes V. Tracy: Basecalling, alignment, assembly and deconvolution of sanger chromatogram trace files.. BMC Genom. 2020;21:230.
    doi: 10.1186/s12864-020-6635-8pmc: PMC7071639pubmed: 32171249google scholar: lookup
  87. Xu S, Li L, Luo X, Chen M, Tang W, Zhan L, Dai Z, Lam TT, Guan Y, Yu G. Ggtree: A serialized data object for visualization of a phylogenetic tree and annotation data.. iMeta 2022;1:5–8.
    doi: 10.1002/imt2.56pmc: PMC10989815pubmed: 38867905google scholar: lookup
  88. Belyaev AS, Chong S, Novikov A, Kongpachith A, Masiarz FR, Lim M, Kim JP. Hepatitis G Virus Encodes Protease Activities Which Can Effect Processing of the Virus Putative Nonstructural Proteins.. J. Virol. 1998;72:868–872.
    doi: 10.1128/JVI.72.1.868-872.1998pmc: PMC109451pubmed: 9420302google scholar: lookup
  89. Qi PF, Gao XY, Ji JK, Zhang Y, Yang SH, Cheng KH, Cui N, Zhu ML, Hu T, Dong X. Identification of a recombinant equine coronavirus in donkey, China.. Emerg. Microbes Infect. 2022;11:1010–1013.
  90. Ramsay JD, Evanoff R, Wilkinson TE, Divers TJ, Knowles DP, Mealey RH. Experimental transmission of equine hepacivirus in horses as a model for hepatitis C virus.. Hepatology 2015;61:1533–1546.
    doi: 10.1002/hep.27689pubmed: 25580897google scholar: lookup

Citations

This article has been cited 0 times.