ArticleInternational journal of molecular sciences2025
A Universal and Quantitative PCR Strategy for Detection and Epidemiologic Analysis of Canine Papillomavirus (CPV).
Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Development and Validation of a Recombinant VP2-Based Indirect ELISA for Canine Parvovirus.Microorganisms · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Canine papillomavirus (CPV) infection leads to a range of clinical manifestations from benign warts to malignant tumors in dogs, posing significant challenges in veterinary medicine due to its diverse genotypic spectrum. This study introduced broad-range and robust polymerase chain reaction (PCR) assays designed to enhance the detection, identification, and quantification of multiple CPV genotypes. By using both universal and genotype-specific primers, this protocol significantly improved diagnostic specificity and sensitivity across the 23 known CPV genotypes compared to previously described ones. The primers were designed to target conserved regions across all genotypes for general detection, as well as specific regions in the predominant genotypes CPV1 and CPV2 for detailed analysis. Validation of this protocol using synthetic plasmids and clinical samples confirmed its enhanced performance over traditional methods, as demonstrated by higher specificity and sensitivity. Additionally, the application of this PCR approach in a series of epidemiological studies provided novel insights into the distribution and prevalence of CPV genotypes, highlighting its potential utility in shaping targeted vaccination and clinical management strategies. Furthermore, the quantitative capability of this established protocol allowed for monitoring viral loads in clinical cases, offering a valuable tool for assessing treatment efficacy and disease progression. Further validation through larger-scale clinical studies will be crucial to substantiate the diagnostic accuracy and epidemiological value of the assays.
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Registered trials
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.