Evidence map›Paper›PMID 39639673›Full record

ArticleJournal of fish diseases2025

18S rRNA Metagenomic Analysis of Nodular Gill Disease in Swiss Rainbow Trout (Oncorhynchus mykiss).

James W Wynne, Chloe J English, Stefania M Vannetti, Megan Rigby, Petra R Quezada-Rodriguez, Ralph Knüsel, Christine Huynh, Heike Schmidt-Posthaus

Abstract read
In one paragraph

Article in Journal of fish diseases, 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

8 authors.

James W WynneCSIRO Agriculture and Food, Hobart, Tasmania, Australia.ORCID https://orcid.org/0000-0001-6846-757X
Chloe J EnglishSchool of Environment, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-9904-493X
Stefania M VannettiDepartment of Infectious Diseases and Pathobiology, Vetsuisse Faculty, Institute for Fish and Wildlife Health, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0009-0003-4050-8941
Megan RigbyCSIRO Agriculture and Food, Hobart, Tasmania, Australia.ORCID https://orcid.org/0000-0002-6268-0414
Petra R Quezada-RodriguezCSIRO Agriculture and Food, Hobart, Tasmania, Australia.ORCID https://orcid.org/0000-0003-3061-4428
Ralph KnüselFishdoc GmbH, Rain, Switzerland.
Christine HuynhNautilus Collaboration, Lucaston, Tasmania, Australia.
Heike Schmidt-PosthausDepartment of Infectious Diseases and Pathobiology, Vetsuisse Faculty, Institute for Fish and Wildlife Health, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0000-0003-2628-4454

Funding

CSIRO Julius Career AwardEuropean Association of Fish Pathologists Small Grant SchemeSwiss Food Safety and Veterinary Officethe Swiss Food Safety and Veterinary Office
6 · The paper itself

Abstract

Nodular gill disease (NGD) is a serious proliferative gill condition that affects farmed salmonids, particularly in Europe. While the cause of NGD remains unknown (and maybe multifactorial), various amoebae are often isolated from the gills of affected fish and can in some cases be seen associated with lesions by histopathology. The present study aimed to quantify the abundance of different amoeba species directly from the gills of rainbow trout affected by NGD and healthy controls. An 18S rRNA amplicon metagenomic approach was employed to profile the diversity and abundance of micro-eukaryotes (including amoebae) while suppressing the amplification of host DNA using a salmonid-specific C3 spacer blocking primer. The 18S rRNA metagenomics approach identified a diversity of micro-eukaryotes on the gills of rainbow trout, including the phylum's Amoebozoa, Diatomea, Platyhelminthes and Ciliophora. Rainbow trout clinically affected by NGD had a significantly higher abundance of a specific sequence (zOTU2) classified as Vannella sp. compared to healthy controls. A quantitative PCR assay was then developed and validated which accurately quantified the abundance of this Vannella sp. sequence from a NGD outbreak in a Swiss rainbow trout farm. Additional PCR and Sanger sequencing analysis of the zOTU2 sequence demonstrated that this sequence is most likely derived from Vannella mustalahtiana. Our study highlights the potential role of Vannella mustalahtiana in NGD in Switzerland and further describes a specific and validated diagnostic PCR assay for accurate detection of this Vannella species.

Indexed as

AmebiasisFish DiseasesOncorhynchus mykissAmoebaAnimalsGillsMetagenomeMetagenomicsRNA, Ribosomal, 18SRNA, Ribosomal, 18SaetiologyAmoebozoaaquaculturegill healthmicro‐eukaryotesVannella

Identifiers

PMID39639673
PMCPMC11837460

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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.