Evidence map›Paper›PMID 36068296›Full record

ArticleNPJ vaccines2022

Development of an attenuated vaccine against Koi Herpesvirus Disease (KHVD) suitable for oral administration and immersion.

Sandro Klafack, Lars Schröder, Yeonhwa Jin, Matthias Lenk, Pei-Yu Lee, Walter Fuchs, Jean-Christophe Avarre, Sven M Bergmann

Abstract read
In one paragraph

Article in NPJ vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. A comprehensive method for quantifying human cytomegalovirus plaque assays.Frontiers in cellular and infection microbiology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Protective effects of immersion immunization of koi withFish and shellfish immunology reports · 2023
    Article
  7. Article
  8. 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

8 authors.

Sandro KlafackFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Infectology, Greifswald, Germany. sandro.klafack@fli.de.ORCID http://orcid.org/0000-0001-6926-6358
Lars SchröderFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Molecular Virology and Cell Biology, Greifswald, Germany.
Yeonhwa JinFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Infectology, Greifswald, Germany.
Matthias LenkFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Department of Experimental Animal Facilities and Biorisk Management (ATB), Greifswald, Germany.ORCID http://orcid.org/0000-0002-1904-3575
Pei-Yu LeeGeneReach Biotechnology Corporation, Taichung, Taiwan.ORCID http://orcid.org/0000-0002-2551-6615
Walter FuchsFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Molecular Virology and Cell Biology, Greifswald, Germany.
Jean-Christophe AvarreISEM, Univ Montpellier, CNRS, IRD, Montpellier, France.ORCID http://orcid.org/0000-0001-6899-7052
Sven M BergmannFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Infectology, Greifswald, Germany. saint_michel@gmx.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the end of the1990ies, Cyprinid herpesvirus 3 (also known as koi herpesvirus, KHV) has caused mass mortality events of koi and common carp all over the globe. This induced a high economic impact, since the KHV disease cannot be cured up to now, but only prevented by vaccination. Unfortunately, there is only one commercial vaccine available which is not approved in most countries. Therefore, there is an urgent need for new, safe and available vaccines. In this study, a live attenuated vaccine virus was generated by cell culture passages of virulent KHV, and shown to protect carp or koi after immersion or oral application against wild type challenge. An advantage of boost immunization was demonstrated, especially after oral application. Vaccination induced no or mild clinical signs and protecting antibodies have been measured. Additionally, the vaccine virus allowed differentiation of infected from vaccinated animals (DIVA) by PCR. The attenuation of the newly generated vaccine was tracked down to a partial deletion of open reading frame 150. This was confirmed by the generation of engineered ORF150 deletion mutants of wild-type KHV which exhibited a similar attenuation in vivo.

Identifiers

PMID36068296
PMCPMC9448810

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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.