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.
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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
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
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.
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.
Cutarelli A, De Falco F, Brunetti R. Molecular detection of transcriptionally active ovine papillomaviruses in commercial equine semen. Front Vet Sci 11:1427370.
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.
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.
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.
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.
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.
De Falco F, Cutarelli A, Leonardi L, Marcus I, Roperto S. Vertical intrauterine bovine and ovine papillomavirus coinfection in pregnant cows. Pathogens 13:453.
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.
Johne R, Müller H, Rector A, van Ranst M, Stevens H. Rolling-circle amplification of viral DNA genomes using phi29 polymerase. Trends Microbiol 17:205–211.
Rousseau MC, Pereira JS, Prado JC, Villa LL, Rohan TE, Franco EL. Cervical coinfection with human papillomavirus (HPV) types as a predictor of acquisition and persistence of HPV infection. J Infect Dis 184:1508–1517.
Munday JS, Knight CG, Bodaan CJ, Codaccioni C, Hardcastle MR. papillomavirus type 7 is a rare cause of equine penile squamous cell carcinomas. Vet J 306:106155.
Munday JS, Fairley R, Lowery I. Detection of papillomavirus type 2 DNA sequences in a sarcoid-like mass in the mouth of a pig. Vet Microbiol 248:108801.
Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP. MrBayes 3.2: efficient bayesian phylogenetic inference and model selection across a large model space. Syst Biol 61:539–542.
Rousseau MC, Abrahamowicz M, Villa LL, Costa MC, Rohan TE, Franco EL. Predictors of cervical coinfection with multiple human papillomavirus types. Cancer Epidemiol Biomarkers Prev 12:1029–1037.
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