Evidence map›Paper›PMID 40670973›Full record

ArticleBMC veterinary research2025

Severe pathological and transcriptional changes in haematopoietic organs of salmon suffering from salmon gill poxvirus disease.

Ottavia Benedicenti, Ole Bendik Dale, Maria K Dahle, Mona C Gjessing

Abstract read
In one paragraph

Article in BMC veterinary research, 2025. 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. Review
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

4 authors.

Ottavia BenedicentiNorwegian Veterinary Institute, Postboks 64, Ås, 1431, Norway. ottavia.benedicenti@vetinst.no.
Ole Bendik DaleNorwegian Veterinary Institute, Postboks 64, Ås, 1431, Norway.
Maria K DahleNorwegian Veterinary Institute, Postboks 64, Ås, 1431, Norway.
Mona C GjessingNorwegian Veterinary Institute, Postboks 64, Ås, 1431, Norway. mona.gjessing@vetinst.no.

Funding

Norges Forskningsråd 303415
6 · The paper itself

Abstract

backgroundInfection with salmon gill poxvirus (SGPV) can lead to acute disease outbreaks with high mortalities caused by extensive gill pathology. In some cases, additional signs of severe red blood cell breakdown (erythrophagocytosis) are present in the spleen and kidney. This can indicate a broader systemic effect of the infection, extending beyond the gills. In a previous study, we investigated the gill histopathology and transcriptome response of salmon sampled from such an outbreak. Here, we further investigate these responses in the same fish, focusing on the haematopoietic organs.

resultsResults show that extensive accumulation of red blood cell breakdown products and phagocytosis of red blood cells were seen in the salmon suffering from salmon gill poxvirus disease. Moreover, differentially expressed genes exhibited an apparent organ-specific pattern, with a primary function involved in immune response, which was predominantly observed in the spleen and kidney. Additional antiviral responses, as well as coagulation and vascular function, apoptosis, and stress responses, were also detected in haematopoietic organs.

conclusionsIn conclusion, salmon gill poxvirus disease (SGPVD) affects haematopoietic organs, causing red blood cell breakdown and organ-specific immune responses. Gene expression patterns highlight immune activation, antiviral defence, coagulation, and stress pathways in the spleen and kidney of salmon suffering from SGPVD.

Indexed as

Fish DiseasesPoxviridaePoxviridae InfectionsSalmonAnimalsGillsKidneySpleenTranscriptomeErythrophagocytosisSalmon gill poxvirusSystemic response

Identifiers

PMID40670973
PMCPMC12265247

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.