Evidence map›Paper›PMID 41600737›Full record

ArticleVeterinary sciences2026

Completion of the Genome Sequence of a Historic CDV Vaccine Strain, Rockborn: Evolutionary and Epidemiologic Implications.

Zsófia Lanszki, Krisztián Bányai, Ágnes Bogdán, Gábor Kemenesi, Georgia Diakoudi, Gianvito Lanave, Francesco Pellegrini, Nicola Decaro, Vito Martella

Abstract read
In one paragraph

Article in Veterinary sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Zsófia LanszkiNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, 7624 Pécs, Hungary.ORCID 0000-0003-3116-4633
Krisztián BányaiDepartment of Medical Biology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Ágnes BogdánDepartment of Medical Biology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Gábor KemenesiNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, 7624 Pécs, Hungary.ORCID 0000-0001-9775-3065
Georgia DiakoudiDepartment of Veterinary Medicine, University of Bari Aldo Moro, 70010 Valenzano, Italy.ORCID 0000-0002-7305-5630
Gianvito LanaveDepartment of Veterinary Medicine, University of Bari Aldo Moro, 70010 Valenzano, Italy.ORCID 0000-0003-4614-677X
Francesco PellegriniDepartment of Veterinary Medicine, University of Bari Aldo Moro, 70010 Valenzano, Italy.ORCID 0000-0003-0026-8472
Nicola DecaroDepartment of Veterinary Medicine, University of Bari Aldo Moro, 70010 Valenzano, Italy.ORCID 0000-0001-6348-7969
Vito MartellaDepartment of Pharmacology and Toxicology, University of Veterinary Medicine, 1078 Budapest, Hungary.ORCID 0000-0002-5740-6947

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The historic Rockborn strain of the canine distemper virus was widely used as a vaccine, but its use was discontinued due to safety concerns. Yet, Rockborn-like canine distemper virus strains are still used in some vaccine formulations. Genetic analysis of this strain was previously limited to the H gene, leaving its full evolutionary and pathogenic potential unclear. This study aimed to determine the complete genome sequence of the Rockborn strain to reconstruct its origin, understand its evolution, and provide a reference for improving diagnostics and future research on virulence markers. An amplicon-based sequencing protocol using MinION nanopore technology was employed to determine the complete genome of the Rockborn-46th laboratory strain. The genome was assembled, annotated, and analyzed in comparison with 223 genomes. The complete genome of the Rockborn strain was 15,690 nucleotides in length. Phylogenetic analysis revealed that Rockborn forms a unique lineage with field isolates from a masked civet in China and a dog in the United States. Crucially, a significant recombination event was identified, showing that the Rockborn strain acted as a parental strain, contributing its F and H genes to create mosaic viruses. The full-genome characterization of the Rockborn strain confirms that Rockborn-like viruses persist and actively contribute to the evolution of canine distemper virus through recombination. This finding highlights the inadequacy of single-gene analysis for diagnostics and surveillance, and underscores the necessity of whole-genome sequencing to accurately track the virus epidemiology and evolution.

Indexed as

canine distemperphylogenetic analysisrecombinationwhole genome sequencing

Identifiers

PMID41600737
PMCPMC12846550

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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.