Evidence map›Paper›PMID 41471184›Full record

ArticlePathogens (Basel, Switzerland)2025

Cell-Free Genomic DNA Release into Serum of Wild Boar and Domestic Pigs Infected with Highly Virulent African Swine Fever Virus.

Ann Sofie Olesen, Louise Lohse, Graham J Belsham

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Ann Sofie OlesenSection for Veterinary Virology, Department of Virology and Microbiological Preparedness, Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen, Denmark.ORCID 0000-0002-6161-3439
Louise LohseSection for Veterinary Virology, Department of Virology and Microbiological Preparedness, Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen, Denmark.ORCID 0000-0002-6769-5447
Graham J BelshamSection for Bacteria and Viruses, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, DK-1870 Frederiksberg, Denmark.ORCID 0000-0003-1187-4873

Funding

European Union's Horizon Europe Project EUPAHW 101136346Fødevarestyrelsen NAStatens Serum Institut NAUniversity of Copenhagen NA
6 · The paper itself

Abstract

African swine fever virus (ASFV) is the cause of a severe hemorrhagic disease in domestic pigs and wild boar. Currently, a highly virulent genotype II ASFV is causing massive pig mortality worldwide. In its acute form, the disease is characterized by high fever, a range of non-specific clinical signs and cell death. In this study, we demonstrate a greatly elevated level (>1000-fold) of cell-free DNA (cfDNA), more specifically, fragmented host genomic DNA (gDNA), in serum from both wild boar and domestic pigs infected with a highly virulent genotype II ASFV. Increases were also observed, to a lesser extent, in the serum levels of mitochondrial DNA (between 4- to >500-fold). For comparison, release of the cytoplasmic enzyme, lactate dehydrogenase, which is a commonly used marker for cellular damage, was also found to be elevated in some animals, but with less consistency. These results indicate that gDNA in serum (i.e., cfDNA) can be a useful marker for cell death during infection with highly virulent variants of the virus, and could be a promising biomarker to elucidate the pathogenesis of ASFV infection in both domestic pigs and wild boar in future studies.

Indexed as

African Swine FeverAfrican Swine Fever VirusCell-Free Nucleic AcidsAnimalsBiomarkersDNA, MitochondrialL-Lactate DehydrogenaseSus scrofaSwineVirulenceBiomarkersCell-Free Nucleic AcidsDNA, MitochondrialL-Lactate DehydrogenaseAfrican swine fever viruscell-damagecell-free DNAgenomic DNAlactate dehydrogenasemitochondrial DNA

Identifiers

PMID41471184
PMCPMC12736371

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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.