Analyze Diet

Bovine and ovine deltapapillomavirus coinfection associated with equine sarcoid.

Abstract: Papillomaviruses (PV) are significant agents capable of inducing simple, multiple, and/or proliferative lesions in the dermis and epidermis of animals, known as cutaneous papillomatosis. These lesions can be benign or malignant and have been identified in various hosts, including mammals, birds, reptiles, and fish. PVs are strictly species- and tissue-specific, although some established and unusual cases of cross-infection, such as BPV in equine sarcoids, have been reported. Sarcoids are horses' most common skin tumors, which can be locally aggressive and cause significant clinical signs. It is recurrently associated with Bos taurus papillomavirus (BPV) and, more recently, Ovis aries papillomavirus (OaPV). Interestingly, OaPV2s, initially identified in sheep, have been detected in other species, such as horses, cattle, and pigs. Therefore, the present study aimed to detect and sequence PVs in an equine sarcoid through rolling circle amplification followed by high-throughput sequencing (RCA-HTS) on the Illumina MiSeq platform. Sequencing yielded 387,923 reads and 17 contigs classified as Deltapapillomavirus genus. A complete BPV1 genome, with 99% coverage, was sequenced, and partial E1 and L1 genes of OaPV2 were detected. Histopathological analysis revealed fibroblastic sarcoid, which has been associated with BPV1 and OaPVs. Our results agree with recent BPV and OaPV2 association observations in sarcoid lesions in equine and swine. This broad host range of OaPVs deserves attention, as it may indicate potential interspecies transmission that is not yet fully understood, especially in coinfections, which could influence viral dynamics, transmission patterns, and disease outcomes. Until now, only OaPV1, 3, and 4 had been detected in equine sarcoids; thus, this is the first detection of OaPV2 in an equine sarcoid. In conclusion, OaPV2 should be considered a potential etiological agent of sarcoids, particularly in association with BPV1.
Publication Date: 2025-08-22 PubMed ID: 40844556PubMed Central: PMC12660604DOI: 10.1007/s42770-025-01759-xGoogle 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 research investigates the presence of bovine and ovine deltapapillomaviruses in equine sarcoid tumors, providing evidence of coinfection and expanding knowledge on viral involvement in these common horse skin tumors.

Background on Papillomaviruses and Sarcoids

  • Pv Characteristics:
    • PVs are viruses that cause skin lesions—including papillomas or tumors—in a wide variety of animals such as mammals, birds, reptiles, and fish.
    • They typically have strict species and tissue specificity, meaning each virus usually infects certain species and tissue types.
    • However, some exceptions exist where PVs infect other species, which is unusual but reported, like bovine papillomavirus (BPV) in horses.
  • Sarcoids in Horses:
    • Sarcoids are the most common skin tumors in horses and are characterized by aggressive but non-metastatic growth.
    • They cause clinical issues due to their persistence and local invasiveness.
    • Previous studies link sarcoids primarily to BPV, especially BPV1 and BPV2.
    • More recently, ovine papillomaviruses (OaPV), specifically found in sheep, have also been implicated in these tumors.
  • Cross-Species Infection:
    • OaPV2, initially discovered in sheep, has been detected in various other species including horses, cattle, and pigs.
    • This cross-species detection raises questions about interspecies viral transmission and its implications.

Research Aim and Methodology

  • The study aimed to detect and analyze papillomavirus genomes in an equine sarcoid sample.
  • Techniques used:
    • Rolling Circle Amplification (RCA): A technique to amplify circular viral DNA efficiently.
    • High-Throughput Sequencing (HTS) on Illumina MiSeq platform: Allowed comprehensive sequencing and identification of papillomavirus genomes in the sample.
  • Data generated:
    • 387,923 sequencing reads
    • 17 contigs classified into the Deltapapillomavirus genus

Key Findings

  • Viral Genomes Detected:
    • A nearly complete genome of BPV1 was sequenced with 99% coverage.
    • Partial sequences of the E1 and L1 genes of OaPV2 were identified, indicating coinfection.
  • Histopathology:
    • The lesion was confirmed to be a fibroblastic sarcoid, a type commonly associated with BPV1 and ovine papillomaviruses.
  • Novelty:
    • This is the first reported detection of OaPV2 in an equine sarcoid.
    • Previously, only OaPV1, 3, and 4 had been found in such lesions.

Implications and Conclusions

  • Broadened Host Range:
    • The detection of OaPV2 in horses suggests a wider host range for these viruses than previously recognized.
    • This might mean interspecies transmission is occurring but not yet fully understood.
  • Coinfection Impact:
    • Coexistence of BPV1 and OaPV2 in sarcoids could influence how viruses interact, their transmission dynamics, and disease severity or outcomes.
  • Etiological Considerations:
    • OaPV2 should be considered a potential causative agent in sarcoids, especially when found alongside BPV1.
  • Future Directions:
    • Further research is needed to understand mechanisms of cross-species infection and coinfection effects.
    • Understanding these viral dynamics might guide better diagnosis, treatment, and prevention strategies for equine sarcoids.

Cite This Article

APA
Pereira EL, Pereira GR, Osório ML, Terra JLA, Gayger JB, Gularte JS, Demoliner M, Pereira VMAG, Filippi M, de Matos QS, Tessman A, Canal CW, Daudt C, Silva FC, Sita A, Fleck JS, Weber MN, Almeida PR, Spilki FR, da Silva MS. (2025). Bovine and ovine deltapapillomavirus coinfection associated with equine sarcoid. Braz J Microbiol, 56(4), 2901-2908. https://doi.org/10.1007/s42770-025-01759-x

Publication

ISSN: 1678-4405
NlmUniqueID: 101095924
Country: Brazil
Language: English
Volume: 56
Issue: 4
Pages: 2901-2908

Researcher Affiliations

Pereira, E L
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Pereira, G R
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Osório, M L de
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Terra, J L A
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Gayger, J B
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Gularte, J S
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Demoliner, M
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Pereira, V M A G
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Filippi, M
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
de Matos, Q S
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Tessman, A
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Canal, C W
  • Laboratório de Virologia Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Daudt, C
  • Laboratório de Virologia Geral e Parasitologia, Universidade Federal do Acre, Rio Branco, AC, Brazil.
Silva, F C
  • Laboratório de Virologia Geral e Parasitologia, Universidade Federal do Acre, Rio Branco, AC, Brazil.
Sita, A
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Fleck, J S
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Weber, M N
  • Laboratório de Imunologia e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Almeida, P R
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Spilki, F R
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
da Silva, M S
  • ¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil. marianasilva2@feevale.br.

MeSH Terms

  • Animals
  • Horses
  • Horse Diseases / virology
  • Horse Diseases / pathology
  • Papillomavirus Infections / veterinary
  • Papillomavirus Infections / virology
  • Coinfection / veterinary
  • Coinfection / virology
  • Cattle
  • Skin Neoplasms / veterinary
  • Skin Neoplasms / virology
  • Skin Neoplasms / pathology
  • Sheep
  • Deltapapillomavirus / genetics
  • Deltapapillomavirus / isolation & purification
  • Deltapapillomavirus / classification
  • Cattle Diseases / virology
  • Sheep Diseases / virology
  • Phylogeny
  • Genome, Viral

Grant Funding

  • 405786/2022-0 / Conselho Nacional de Desenvolvimento Científico e Tecnológico
  • 001 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
  • 23/2551-0002221-4 / Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Conflict of Interest Statement

Declarations. Competing Interests: The authors declare that they have no competing interests.

References

This article includes 37 references
  1. Alberti A, Pirino S, Pintore F, Addis MF, Chessa B, Cacciotto C, Cubeddu T, Anfossi A, Benenati G, Coradduzza E, Lecis R, Antuofermo E, Carcangiu L, Pittau M. papillomavirus 3: a prototype of a novel genus in the family associated with ovine squamous cell carcinoma. Virology 407:352–359.
    doi: 10.1016/j.virol.2010.08.036pubmed: 20863546google scholar: lookup
  2. Bernard HU, Burk RD, Chen Z, van Doorslaer K, zur Hausen H, de Villiers EM. Classification of papillomaviruses (PVs) based on 189 PV types and proposal of taxonomic amendments. Virology 401:70–79.
    doi: 10.1016/j.virol.2010.02.002pmc: PMC3400342pubmed: 20206957google scholar: lookup
  3. Cutarelli A, De Falco F, Brunetti R. Molecular detection of transcriptionally active ovine papillomaviruses in commercial equine semen. Front Vet Sci 11:1427370.
    doi: 10.3389/fvets.2024.1427370pmc: PMC11253197pubmed: 39021410google scholar: lookup
  4. Cutarelli A, Passantino G, Razzuoli E. Digital droplet PCR-based detection and quantification of ovine papillomavirus DNA from the vaginal virobiota of healthy mares. Sci Rep 15:9951.
    doi: 10.1038/s41598-025-94279-5pmc: PMC11929744pubmed: 40121289google scholar: lookup
  5. Daudt C, da Silva FRC, Cibulski SP, Streck AF, Laurie RE, Munday JS, Canal CW. Bovine papillomavirus 24: a novel member of the genus detected in the Amazon region. Arch Virol 164:313–321.
    doi: 10.1007/s00705-018-4092-3pubmed: 30417199google scholar: lookup
  6. Daudt C, Da Silva FRC, Streck AF, Weber MN, Mayer FQ, Cibulski SP, Canal CW. How many papillomavirus species can go undetected in papilloma lesions?. Sci Rep 6:36480.
    doi: 10.1038/srep36480pmc: PMC5093584pubmed: 27808255google scholar: lookup
  7. Daudt C, Da Silva FRC, Lunardi M. Papillomaviruses in ruminants: an update. Transbound Emerg Dis 65:1381–1395.
    doi: 10.1111/tbed.12868pubmed: 29603890google scholar: lookup
  8. De Falco F, Cutarelli A, Cuccaro B, Catoi C, De Carlo E, Roperto S. Evidence of a novel cross-species transmission by ovine papillomaviruses. Transbound Emerg Dis 69:e3229–e3237.
    doi: 10.1111/tbed.14756pubmed: 36335589google scholar: lookup
  9. De Falco F, Cuccaro B, De Tullio R, Alberti A, Cutarelli A, De Carlo E, Roperto S. Possible etiological association of ovine papillomaviruses with bladder tumors in cattle. Virus Res 328:199084.
  10. De Falco F, Cutarelli A, Pellicanò R, Brandt S, Roperto S. Molecular detection and quantification of ovine papillomavirus DNA in equine sarcoid. Transbound Emerg Dis 2024:6453158.
    doi: 10.1155/2024/6453158pmc: PMC12016688pubmed: 40303025google scholar: lookup
  11. De Falco F, Cutarelli A, Leonardi L, Marcus I, Roperto S. Vertical intrauterine bovine and ovine papillomavirus coinfection in pregnant cows. Pathogens 13:453.
    doi: 10.3390/pathogens13060453pmc: PMC11206582pubmed: 38921751google scholar: lookup
  12. De Villiers EM, Fauquet C, Broker TR, Bernard HU, zur Hausen H. Classification of papillomaviruses. Virology 324:17–27.
    doi: 10.1016/j.virol.2004.03.033pubmed: 15183049google scholar: lookup
  13. Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32:1792–1797.
    doi: 10.1093/nar/gkh340pmc: PMC390337pubmed: 15034147google scholar: lookup
  14. Forslund O, Antonsson A, Nordin P, Stenquist B, Hansson BG. A broad range of human papillomavirus types was detected using a general PCR method suitable for analyzing cutaneous tumours and normal skin. J Gen Virol 80:2437–2443.
    doi: 10.1099/0022-1317-80-9-2437pubmed: 10501499google scholar: lookup
  15. Gibbs EP, Smale CJ, Lawman MJ. Warts in sheep: identification of a papilloma virus and transmission of infection to sheep. J Comp Pathol 85:327–334.
    doi: 10.1016/0021-9975(75)90075-4pubmed: 167057google scholar: lookup
  16. Goldschmidt MH et al (2018) Surgical pathology of tumors of domestic animals volume 1: epithelial tumors of the skin. Kiupel M (ed). 10.1177/0300985818825245
  17. Johne R, Müller H, Rector A, van Ranst M, Stevens H (2009) Rolling-circle amplification of viral DNA genomes using phi29 polymerase. Trends Microbiol 17:205–211. 10.1016/j.tim.2009.02.004
    doi: 10.1016/j.tim.2009.02.004pubmed: 19375325google scholar: lookup
  18. Hainisch EK, Jindra C, Reicher P, Miglinci L, Brodesser DM, Brandt S (2022) Bovine papillomavirus type 1 or 2 virion-infected primary fibroblasts constitute a near-natural equine sarcoid model. Viruses 14:2665. 10.3390/v14122658
    doi: 10.3390/v14122658pmc: PMC9781842pubmed: 36560661google scholar: lookup
  19. Karalus W, Subharat S, Orbell G, Vaatstra B, Munday JS (2024) Equine sarcoids: A clinicopathologic study of 49 cases, with mitotic count and clinical type predictive of recurrence. Vet Pathol 61:XXX–XXX. 10.1177/03009858231209408
    doi: 10.1177/03009858231209408pmc: PMC11067406pubmed: 37937724google scholar: lookup
  20. Kaynarcalidan O, Oğuzoğlu TÇ (2021) The oncogenic pathways of papillomaviruses. Vet Comp Oncol 19:XXX. 10.1111/vco.12659. XXX
    doi: 10.1111/vco.12659pubmed: 33084187google scholar: lookup
  21. Lunardi M, De Alcântara BK, Otonel RAA, Rodrigues WB, Alfieri AF, Alfieri AA (2013) Bovine papillomavirus type 13 DNA in equine sarcoids. J Clin Microbiol 51:2167–2171. 10.1128/JCM.00371-13
    doi: 10.1128/JCM.00371-13pmc: PMC3697707pubmed: 23637294google scholar: lookup
  22. Rousseau MC, Pereira JS, Prado JC, Villa LL, Rohan TE, Franco EL (2001) Cervical coinfection with human papillomavirus (HPV) types as a predictor of acquisition and persistence of HPV infection. J Infect Dis 184:1508–1517. 10.1086/324579
    doi: 10.1086/324579pubmed: 11740725google scholar: lookup
  23. Melinyshyn H (2019) Multiple excisions of an equine sarcoid and the repercussions. Can Vet J 60:1115–1117
    pmc: PMC6741832pubmed: 31597999
  24. Munday JS, Knight CG, Bodaan CJ, Codaccioni C, Hardcastle MR (2024) papillomavirus type 7 is a rare cause of equine penile squamous cell carcinomas. Vet J 306:106155. 10.1016/j.tvjl.2024.106155n
    doi: 10.1016/j.tvjl.2024.106155pubmed: 38838769google scholar: lookup
  25. Munday JS (2014) Bovine and human papillomaviruses: a comparative review. Vet Pathol 51:1063–1075. 10.1177/0300985814537837
    doi: 10.1177/0300985814537837pubmed: 24981715google scholar: lookup
  26. Munday JS, Fairley R, Lowery I (2020) Detection of papillomavirus type 2 DNA sequences in a sarcoid-like mass in the mouth of a pig. Vet Microbiol 248:108801. 10.1016/j.vetmic.2020.108801n
    doi: 10.1016/j.vetmic.2020.108801pubmed: 32827929google scholar: lookup
  27. Munday JS, Gedye K, Daudt C, Da Silva FC (2021) The development of novel primer sets to specifically amplify each of the five different deltapapillomaviruses that cause neoplasia after cross-species infection. Vet Sci 8:207. 10.3390/vetsci8100208
    doi: 10.3390/vetsci8100208pmc: PMC8541201pubmed: 34679038google scholar: lookup
  28. Munday JS, Kiupel M (2010) Papillomavirus-associated cutaneous neoplasia in mammals. Vet Pathol 47:254–264. 10.1177/0300985809358604
    doi: 10.1177/0300985809358604pubmed: 20106770google scholar: lookup
  29. Munday JS, Orbell G, Fairley RA, Hardcastle M, Vaatstra B (2021) Evidence from a series of 104 equine sarcoids suggests that most sarcoids in new Zealand are caused by bovine papillomavirus type 2, although both BPV1 and BPV2 DNA are detectable in around 10% of sarcoids. Animals 11:3093. 10.3390/ani11113093
    doi: 10.3390/ani11113093pmc: PMC8614326pubmed: 34827825google scholar: lookup
  30. Kalantar KL, Carvalho T, Bourcy CFA et al (2020) IDseq—An open-source cloud-based pipeline and analysis service for metagenomic pathogen detection and monitoring. GigaScience 9:giaa111. 10.1093/gigascience/giaa111
    doi: 10.1093/gigascience/giaa111pmc: PMC7566497pubmed: 33057676google scholar: lookup
  31. Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP (2012) MrBayes 3.2: efficient bayesian phylogenetic inference and model selection across a large model space. Syst Biol 61:539–542
    doi: 10.1093/sysbio/sys029pmc: PMC3329765pubmed: 22357727google scholar: lookup
  32. Rousseau MC, Abrahamowicz M, Villa LL, Costa MC, Rohan TE, Franco EL (2003) Predictors of cervical coinfection with multiple human papillomavirus types. Cancer Epidemiol Biomarkers Prev 12:1029–1037
    pubmed: 14578139
  33. Sauthier JT, Daudt C, da Silva FRC et al (2021) The genetic diversity of papillomavirome in bovine teat papilloma lesions. Anim Microbiome 3:14. 10.1186/s42523-021-00114-3
    doi: 10.1186/s42523-021-00114-3pmc: PMC8317299pubmed: 34321106google scholar: lookup
  34. Semik-Gurgul E (2021) Molecular approaches to equine sarcoids. Equine Vet J 53:XXX. 10.1111/evj.13322. XXX
    doi: 10.1111/evj.13322pubmed: 32654178google scholar: lookup
  35. Taylor S, Haldorson G (2013) A review of equine mucocutaneous squamous cell carcinoma. Equine Vet Educ 25:374–378. 10.1111/j.2042-3292.2012.00457.x
  36. Teifke JP, Kidney BA, Löhr CV, Yager JA (2003) Detection of papillomavirus-DNA in mesenchymal tumour cells and not in the hyperplastic epithelium of feline sarcoids. Vet Dermatol 14:47–51. 10.1046/j.1365-3164.2003.00324.x
  37. Ogłuszka M, Starzyński RR, Pierzchała M, Otrocka-Domagała I, Raś A (2021) Equine sarcoids—causes, molecular changes, and clinicopathologic features: a review. Vet Pathol 58:472–482
    doi: 10.1177/0300985820985114pubmed: 33461443google scholar: lookup

Citations

This article has been cited 0 times.