Evidence map›Paper›PMID 40844556›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2025

Bovine and ovine deltapapillomavirus coinfection associated with equine sarcoid.

E L Pereira, G R Pereira, M L de Osório, J L A Terra, J B Gayger, J S Gularte, M Demoliner, V M A G Pereira, M Filippi, Q S de Matos and 10 more

Abstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

E L Pereira¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
G R Pereira¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
M L de Osório¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
J L A Terra¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
J B Gayger¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
J S Gularte¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
M Demoliner¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
V M A G Pereira¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
M Filippi¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
Q S de Matos¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
A Tessman¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
C W CanalLaboratório de Virologia Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
C DaudtLaboratório de Virologia Geral e Parasitologia, Universidade Federal do Acre, Rio Branco, AC, Brazil.
F C SilvaLaboratório de Virologia Geral e Parasitologia, Universidade Federal do Acre, Rio Branco, AC, Brazil.
A Sita¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
J S Fleck¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
M N WeberLaboratório de Imunologia e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
P R Almeida¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
F R Spilki¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil.
M S da Silva¹Laboratório de Microbiologia Molecular, Universidade Feevale, Novo Hamburgo, RS, Brazil. marianasilva2@feevale.br.ORCID https://orcid.org/0000-0003-1830-9017

Funding

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

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.

Indexed as

Cattle DiseasesCoinfectionDeltapapillomavirusHorse DiseasesPapillomavirus InfectionsSheep DiseasesSkin NeoplasmsAnimalsCattleGenome, ViralHorsesPhylogenySheepCoinfectionCross-species transmissionMetagenomicsPapillomavirusSarcoid

Identifiers

PMID40844556
PMCPMC12660604

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.