Evidence map›Paper›PMID 40002990›Full record

ArticleAnimals : an open access journal from MDPI2025

Genomic Mosaicism in Fowl Adenovirus 3 Strains.

Zalán Homonnay, Szilvia Jakab, Szilvia Marton, Marianna Domán, Krisztina Bali, Eszter Kaszab, Gábor Kemenesi, Tamás Mató, István Kiss, Vilmos Palya and 1 more

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2025. 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

11 authors.

Zalán HomonnayCeva-Phylaxia Ltd., Szállás u. 5, H-1107 Budapest, Hungary.ORCID 0000-0003-2473-1775
Szilvia JakabHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.ORCID 0009-0005-8435-5507
Szilvia MartonHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.
Marianna DománHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.ORCID 0000-0002-1823-9971
Krisztina BaliHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.
Eszter KaszabHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.ORCID 0000-0002-5750-1872
Gábor KemenesiNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, H-7624 Pécs, Hungary.ORCID 0000-0001-9775-3065
Tamás MatóCeva-Phylaxia Ltd., Szállás u. 5, H-1107 Budapest, Hungary.
István KissCeva-Phylaxia Ltd., Szállás u. 5, H-1107 Budapest, Hungary.ORCID 0000-0001-7839-4415
Vilmos PalyaCeva-Phylaxia Ltd., Szállás u. 5, H-1107 Budapest, Hungary.ORCID 0000-0003-3319-9995
Krisztián BányaiHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.

Funding

National Research, Development and Innovation Fund ÚNKP-23-4 New National Excellence Program of the Ministry for Culture and InnovationNational Research, Development and Innovation Office, Hungary RRF-2.3.1-21-2022-00001National Research, Development and Innovation Office, Hungary RRF-2.3.1-21-2022-00010National Scientific Research Fund of Hungary (OTKA) K120201
6 · The paper itself

Abstract

Fowl adenovirus D is the main cause of inclusion body hepatitis in chickens. Whole genome sequencing was carried out to enrich the genomic sequence database using field isolates of FAdV-D. Out of 44 newly determined genomes, 43 were classified into FAdV-2/-11 and 2 into FAdV-3; no FAdV-9 was identified. Whole-genome based phylogeny showed that FAdV-3 was more distantly related to FAdV 9 and FAdV-2/-11 than FAdV-9 and FAdV-2/-11 to each other. Whole-genome sequence homology analysis revealed that the full-length FAdV-3 genome harbored a ~12 kbp fragment of the genome that shared moderate sequence homology with representative strains of other FAdV-D serotypes but high relatedness with only the FAdV-3 strain whose full-genome is available in GenBank. A closer look onto the fiber and the penton genes of our FAdV-3 isolate identified putative recombination events; both the fiber and the penton coding genes shared fragments originating from FAdV-9. Of interest, ORF19 displayed a close relationship with the homologous genomic region of some FAdV-E strains (amino acid sequence homology, up to 82%). Thus, although FAdV-3 is classified into FAdV-D, the genomic structure of FAdV-3 appears to result from multiple heterotypic and heterologous recombination events. This study highlights the unique origin of FAdV-3.

Indexed as

aviadenovirusesAviadenovirus gallinaeinclusion body hepatitisphylogenetic analysispoultryrecombination analysis

Identifiers

PMID40002990
PMCPMC11851969

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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.