Evidence map›Paper›PMID 32467979›Full record

ArticleGenome biology and evolution2020

Transcriptome-Wide Comparisons and Virulence Gene Polymorphisms of Host-Associated Genotypes of the Cnidarian Parasite Ceratonova shasta in Salmonids.

Gema Alama-Bermejo, Eli Meyer, Stephen D Atkinson, Astrid S Holzer, Monika M Wiśniewska, Martin Kolísko, Jerri L Bartholomew

Open access · goldAbstract readComparative Study
In one paragraph

Article in Genome biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Parasitology · 2022
    Review
  4. Article
  5. Identification ofFrontiers in cellular and infection microbiology · 2022
    Article
  6. Article
  7. Article
  8. Proteases as Therapeutic Targets Against the Parasitic CnidarianFrontiers in cellular and infection microbiology · 2021
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
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

7 authors at 4 institutions in 3 countries.

Gema Alama-BermejoDepartment of Microbiology, Oregon State University.
Eli MeyerDepartment of Integrative Biology, Oregon State University.
Stephen D AtkinsonDepartment of Microbiology, Oregon State University.
Astrid S HolzerInstitute of Parasitology, Biology Centre of the Czech Academy of Sciences, České Budějovice, Czech Republic.
Monika M WiśniewskaInstitute of Parasitology, Biology Centre of the Czech Academy of Sciences, České Budějovice, Czech Republic.
Martin KolískoInstitute of Parasitology, Biology Centre of the Czech Academy of Sciences, České Budějovice, Czech Republic.
Jerri L BartholomewDepartment of Microbiology, Oregon State University.
Oregon State University · USCzech Academy of Sciences, Biology Centre · CZInstitute of Parasitology · CZUniversity of South Bohemia in České Budějovice · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ceratonova shasta is an important myxozoan pathogen affecting the health of salmonid fishes in the Pacific Northwest of North America. Ceratonova shasta exists as a complex of host-specific genotypes, some with low to moderate virulence, and one that causes a profound, lethal infection in susceptible hosts. High throughput sequencing methods are powerful tools for discovering the genetic basis of these host/virulence differences, but deep sequencing of myxozoans has been challenging due to extremely fast molecular evolution of this group, yielding strongly divergent sequences that are difficult to identify, and unavoidable host contamination. We designed and optimized different bioinformatic pipelines to address these challenges. We obtained a unique set of comprehensive, host-free myxozoan RNA-seq data from C. shasta genotypes of varying virulence from different salmonid hosts. Analyses of transcriptome-wide genetic distances and maximum likelihood multigene phylogenies elucidated the evolutionary relationship between lineages and demonstrated the limited resolution of the established Internal Transcribed Spacer marker for C. shasta genotype identification, as this marker fails to differentiate between biologically distinct genotype II lineages from coho salmon and rainbow trout. We further analyzed the data sets based on polymorphisms in two gene groups related to virulence: cell migration and proteolytic enzymes including their inhibitors. The developed single-nucleotide polymorphism-calling pipeline identified polymorphisms between genotypes and demonstrated that variations in both motility and protease genes were associated with different levels of virulence of C. shasta in its salmonid hosts. The prospective use of proteolytic enzymes as promising candidates for targeted interventions against myxozoans in aquaculture is discussed. We developed host-free transcriptomes of a myxozoan model organism from strains that exhibited different degrees of virulence, as a unique source of data that will foster functional gene analyses and serve as a base for the development of potential therapeutics for efficient control of these parasites.

Indexed as

AnimalsDNA ContaminationGenotypeHost-Parasite InteractionsMyxozoaOncorhynchus mykissPhylogenyPolymorphism, Single NucleotideTranscriptomeVirulence FactorsVirulence Factorsaquaculturecell migration/motilityMyxozoaproteasesSNPs

Identifiers

PMID32467979
PMCPMC7487138
OpenAlexW3031110349

What OpenQuestion holds

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LicenceCC BY-NC
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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.