Evidence map›Paper›PMID 33986444›Full record

ArticleScientific reports2021

Detection and quantification of bovine papillomavirus DNA by digital droplet PCR in sheep blood.

Sante Roperto, Anna Cutarelli, Federica Corrado, Francesca De Falco, Canio Buonavoglia

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 26% of its field
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

14 citing papers in PubMed, 17 citations in OpenAlex.

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  9. Detection and Quantification ofPathogens (Basel, Switzerland) · 2023
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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

5 authors at 3 institutions in 1 country.

Sante RopertoDipartimento di Medicina Veterinaria e Produzioni Animali, Università degli Studi di Napoli Federico II, Via Veterinaria, 1, 80137, Naples, Italy. sante.roperto@unina.it.
Anna CutarelliIstituto Zooprofilattico Sperimentale del Mezzogiorno, Via della Salute 2, 80055, Portici, Naples, Italy.
Federica CorradoIstituto Zooprofilattico Sperimentale del Mezzogiorno, Via della Salute 2, 80055, Portici, Naples, Italy.
Francesca De FalcoDipartimento di Medicina Veterinaria e Produzioni Animali, Università degli Studi di Napoli Federico II, Via Veterinaria, 1, 80137, Naples, Italy.
Canio BuonavogliaDipartimento di Medicina Veterinaria, Università degli Studi di Bari "Aldo Moro", Strada Provinciale per Casamassima Km3, 70010, Valenzano, Bari, Italia.
Istituto Zooprofilattico Sperimentale del Mezzogiorno · ITUniversity of Naples Federico II · ITUniversity of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Highly pathogenic bovine papillomaviruses (BPVs) were detected and quantified for the first time using digital droplet polymerase chain reaction (ddPCR) by liquid biopsy in 103 clinically healthy sheep. Overall, ddPCR detected BPVs in 68 blood samples (66%). BPV infection by a single genotype was revealed in 61.8% of the blood samples, and BPV coinfection by double, triple or quadruple genotypes was observed in 38.2% of liquid biopsies. The BPV-2 genotype was most frequently seen in sheep, whereas BPV-1 was the least common. Furthermore, ddPCR was very useful for detection and quantification; the BPV-14 genotype was observed for the first time in ovine species, displaying the highest prevalence in some geographical areas (Apulia). In 42 of the positive samples (61.8%), a single BPV infection was observed, 26 of which were caused by BPV-2 (61.9%) and 7 by BPV-13 (16.7%). BPV-14 was responsible for 7 single infections (16.7%) and BPV-1 for 2 single infections (4.7%). Multiple BPV coinfections were observed in the remaining 26 positive samples (38.2%), with dual BPV-2/BPV-13 infection being the most prevalent (84.6%). BPV infection by triple and quadruple genotypes was also observed in 11.5% and 3.8% of cases, respectively. The present study showed that ddPCR, a biotechnological refinement of conventional PCR, is by far the most sensitive and accurate assay for BPV detection compared to conventional qPCR. Therefore, ddPCR displayed an essential diagnostic and epidemiological value very useful for the identification of otherwise undetectable BPV genotypes as well as their geographical distributions and suggesting that animal husbandry practices contribute to cross-species transmission of BPVs.

Indexed as

AnimalsBovine papillomavirus 1CattleDNA, ViralGenes, ViralGenotypeLiquid BiopsyPolymerase Chain ReactionSheepDNA, Viral

Identifiers

PMID33986444
PMCPMC8119674
OpenAlexW3128485993

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.