Evidence map›Paper›PMID 42321797›Full record

ArticleBMC veterinary research2026

High genetic diversity of porcine rotavirus A, B, and C in Hungary with putative novel VP4 genotypes.

Barbara Igriczi, Luca Zsiborás, Ervin Albert, Zoltán Német, Gyula Balka, Lilla Dénes

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Article in BMC veterinary research, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Barbara IgricziDepartment of Pathology, University of Veterinary Medicine, István Str. 2, Budapest, 1078, Hungary.
Luca ZsiborásDepartment of Pathology, University of Veterinary Medicine, István Str. 2, Budapest, 1078, Hungary.
Ervin AlbertDepartment of Pathology, University of Veterinary Medicine, Üllő, Hungary.
Zoltán NémetDepartment of Pathology, University of Veterinary Medicine, Üllő, Hungary. nemet.zoltan@univet.hu.
Gyula BalkaDepartment of Pathology, University of Veterinary Medicine, István Str. 2, Budapest, 1078, Hungary. balka.gyula@univet.hu.
Lilla DénesDepartment of Pathology, University of Veterinary Medicine, István Str. 2, Budapest, 1078, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRotaviruses (RVs) are important enteric pathogens of swine, contributing significantly to neonatal and post-weaning diarrhea worldwide. Although rotavirus A (RVA) is the best characterized species, much less is known about the epidemiology and genetic diversity of RVB and RVC, especially in Central Europe. This study aimed to investigate the presence and genetic diversity of RVA, RVB, and RVC in diarrheic piglets in Hungary using Nanopore third-generation sequencing.

resultsA total of 77 fecal swab samples collected from diarrheic piglets across 19 swine farms were analyzed. All three RV species were detected, RVA and RVC were each identified in 54.5% of samples, while 40.3% was RVB positive. Coinfections involving multiple RV species were frequent, highlighting the complex etiology of piglet diarrhea. Altogether, 8 RVA, 3 RVB, and 4 RVC full-genome sequences, comprising all 11 segments, were identified. Genotyping of RVA strains revealed multiple G/P genotype combinations, with G9P[23] being the most prevalent. Whole-genome analysis demonstrated a Wa-like genomic backbone of porcine origin. In RVB, three complete VP4 sequences were obtained that could not be assigned to any known P genotype, suggesting the presence of a novel lineage. Hungarian RVC strains showed high genetic diversity, including five distinct G genotypes and one potential novel P genotype, underlining evolutionary diversity of porcine RVs.

conclusionsThis study provides a comprehensive molecular characterization of RVA, RVB, and RVC circulating in Hungarian pig populations. The high prevalence of coinfections and the detection of genetically diverse and potentially novel strains emphasize the complexity of RV epidemiology in swine. These findings highlight the need for continued surveillance to better understand their role in pig health and zoonotic risk.

Indexed as

Genetic VariationRotavirusRotavirus InfectionsSwine DiseasesAnimalsCapsid ProteinsDiarrheaFecesGenotypeHungaryPhylogenySwineCapsid ProteinsVP4 protein, RotavirusEpidemiologyGenetic diversityHungaryNanopore sequencingPorcine rotavirus

Identifiers

PMID42321797
PMCPMC13527926

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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.