Evidence map›Paper›PMID 41983426›Full record

ArticleJournal of fish diseases2026

Salt Treatment Confers Protection Against Acute Carp Edema Virus Reinfection While Promoting Viral Persistence.

Mikolaj Adamek, Maria Zawisza, Justin Tze Ho Chan, Alexander Rebl, Felix Teitge, Alberto Falco, Anne-Carina Miebach, Verena Jung-Schroers, Esteban Soto, Jiří Kyslík and 3 more

Abstract read
In one paragraph

Article in Journal of fish diseases, 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. 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

13 authors.

Mikolaj AdamekFish Disease Research Unit, Institute for Parasitology, University of Veterinary Medicine Hannover, Hannover, Germany.ORCID https://orcid.org/0000-0003-4890-3164
Maria ZawiszaDepartment of Evolutionary Immunology, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Krakow, Poland.
Justin Tze Ho ChanFish Health Division, University of Veterinary Medicine, Vienna, Austria.
Alexander ReblInstitute of Genome Biology, Research Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Felix TeitgeFish Disease Research Unit, Institute for Parasitology, University of Veterinary Medicine Hannover, Hannover, Germany.
Alberto FalcoSpanish National Research Council (IATS-CSIC), Institute of Aquaculture Torre de la Sal, Cabanes, Spain.
Anne-Carina MiebachFish Disease Research Unit, Institute for Parasitology, University of Veterinary Medicine Hannover, Hannover, Germany.
Verena Jung-SchroersFish Disease Research Unit, Institute for Parasitology, University of Veterinary Medicine Hannover, Hannover, Germany.ORCID https://orcid.org/0000-0002-2628-2611
Esteban SotoDepartment of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, California, USA.ORCID https://orcid.org/0000-0001-6054-9634
Jiří KyslíkLaboratory of Fish Immunology, Biology Centre, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czechia.ORCID https://orcid.org/0000-0002-0006-1343
Dieter SteinhagenFish Disease Research Unit, Institute for Parasitology, University of Veterinary Medicine Hannover, Hannover, Germany.ORCID https://orcid.org/0000-0002-2303-8533
Krzysztof RakusDepartment of Evolutionary Immunology, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0002-3739-1514
Tomas KorytarLaboratory of Fish Immunology, Biology Centre, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czechia.

Funding

Deutsche Forschungsgemeinschaft 426513195European Commission 101084204 Cure4AquaNarodowe Centrum Nauki UMO-2018/31/F/NZ6/02311
6 · The paper itself

Abstract

Carp edema virus (CEV) infects the common carp (Cyprinus carpio) and causes the lethal koi sleepy disease (KSD). Signs of KSD include respiratory, detoxification, and osmoregulatory difficulties. Salt treatment re-equilibrates blood sodium levels and can save the fish. However, it is unclear whether these fish are immunized, remain chronically infected, and shed the virus, which could cause concern for aquaculture and the international fish trade. To address this issue, we examined the physiological and immunological responses following the infection of naturally immunized and naïve fish. Primary CEV infection induces inflammation in the gills and recruits granulocytic leukocyte infiltrates to the lamellae. Immunologically, the antiviral response driven by type I interferon is activated; however, both T and B lymphocytes fail to respond. As part of an immunization strategy, a primary infection followed by salt treatment effectively nullifies the pro-inflammatory response and lymphocyte immunosuppression during CEV reinfection. Our data indicate that immunization enables mechanisms such as lymphocyte activation, differentiation, antigen presentation, and an adaptive immune response and antibody production. However, immunized fish are unable to fully clear the virus for a significant period, during which they are most likely to shed infectious particles.

Indexed as

CarpsFish DiseasesPoxviridaePoxviridae InfectionsSodium ChlorideAnimalsImmunizationReinfectionSodium ChlorideB‐cellsCEVKSDnatural immunizationsalt treatment

Identifiers

PMID41983426
PMCPMC13432179

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.