Evidence map›Paper›PMID 42068381›Full record

ArticleVeterinary research communications2026

Molecular insights into domestic cat hepatitis B virus linking genome to function.

Sofija Šolaja, Vesna Milićević, Dimitrije Glišić, Andrea Radalj, Miloš Đurić, Aleksandra Knežević, Jakov Nišavić

Abstract read
In one paragraph

Article in Veterinary research communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

7 authors.

Sofija ŠolajaDepartment of Virology, Institute of Veterinary Medicine of Serbia, Janisa Janulisa 14, Belgrade, 11000, Serbia. sofija.solaja@nivs.rs.
Vesna MilićevićDepartment of Virology, Institute of Veterinary Medicine of Serbia, Janisa Janulisa 14, Belgrade, 11000, Serbia.
Dimitrije GlišićDepartment of Virology, Institute of Veterinary Medicine of Serbia, Janisa Janulisa 14, Belgrade, 11000, Serbia.
Andrea RadaljDepartment of Microbiology, Faculty of Veterinary Medicine, University of Belgrade, Bulevar Oslobođenja 18, Belgrade, 11000, Serbia.
Miloš ĐurićDepartment of Equine, Small Animal, Poultry and Wild Animal Diseases, Faculty of Veterinary Medicine, University of Belgrade, Bulevar Oslobođenja 18, Belgrade, 11000, Serbia.
Aleksandra KneževićInstitute of Microbiology and Immunology, Department of Virology, Faculty of Medicine, University of Belgrade, Doktora Subotića 1, Belgrade, Serbia.
Jakov NišavićDepartment of Microbiology, Faculty of Veterinary Medicine, University of Belgrade, Bulevar Oslobođenja 18, Belgrade, 11000, Serbia.

Funding

Sofija Šolaja, The Ministry of Science, Technological Development and Innovation, Serbia 451-03-136/2025-03/200030Sofija Šolaja, The Ministry of Science, Technological Development and Innovation, Serbia 451-03-136/2025-03/200143The Ministry of Science, Technological Development and Innovation, Serbia 451-03-136/2025-03/200030The Ministry of Science, Technological Development and Innovation, Serbia 451-03-136/2025-03/200143
6 · The paper itself

Abstract

Domestic cat hepatitis B virus (DCHBV) is a member of the Hepadnaviridae family and has been associated with hepatocellular carcinoma (HCC) in cats. This study aimed to determine the prevalence of DCHBV and associations with feline immunodeficiency virus (FIV), feline leukaemia virus (FeLV) and feline coronavirus (FCoV) infections in cats in Serbia, and to characterise the detected DCHBV genomes. Whole blood, serum and liver samples from 308 animals were screened by real-time (RT-)PCR for DCHBV, FIV, FeLV, and FCoV. The prevalence of DCHBV was 2.60%, with no significant associations observed between DCHBV infection and age, sex, or coinfection status. Three whole genome sequences were obtained, and phylogenetic analysis demonstrated that the Serbian strains belong to genotype A. Molecular analysis revealed three unique nonsynonymous substitutions in the S ORF. Within the C ORF, a 28-amino acid N-terminal precore region with conserved cysteine residues critical for protein maturation was identified, along with the C-terminal arginine-rich domain. A putative core promoter region was detected, containing two motifs analogous to the pgRNA and pcRNA initiator elements described in hepatitis B virus (HBV). DCHBV sequences contained two 11-bp direct repeats with DR2 located in X ORF and DR1 positioned in the C ORF. This study represents the first report of DCHBV in Serbia, providing new insights into its epidemiology and genomic features. The findings expand current knowledge of its molecular diversity and underscore the importance of genomic characterisation for understanding its role in liver disease development.

Indexed as

Cat DiseasesGenome, ViralHepatitis BHepatitis B virusAnimalsCatsFemaleMalePhylogenyPrevalenceSerbiaCore promoterDCHBVSerbiaViral oncogenesisWGS

Identifiers

PMID42068381
PMCPMC13135525

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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.