Evidence map›Paper›PMID 33484570›Full record

ArticleGenome biology and evolution2021

Gene Duplication and Gain in the Trematode Atriophallophorus winterbourni Contributes to Adaptation to Parasitism.

Natalia Zajac, Stefan Zoller, Katri Seppälä, David Moi, Christophe Dessimoz, Jukka Jokela, Hanna Hartikainen, Natasha Glover

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2021. 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
1.9field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. A NovelBiomolecules · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Trematode Genomics and Proteomics.Advances in experimental medicine and biology · 2024
    Article
  7. Article
  8. 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

8 authors at 4 institutions in 3 countries.

Natalia ZajacEawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland.
Stefan ZollerETH Zurich, Department of Environmental Systems Science, Institute of Integrative Biology, Zurich, Switzerland.
Katri SeppäläEawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland.
David MoiDepartment of Computational Biology, University of Lausanne, Switzerland.
Christophe DessimozDepartment of Computational Biology, University of Lausanne, Switzerland.
Jukka JokelaEawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland.
Hanna HartikainenEawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland.
Natasha GloverDepartment of Computational Biology, University of Lausanne, Switzerland.
ETH Zurich · CHSIB Swiss Institute of Bioinformatics · CHUniversität Innsbruck · ATUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene duplications and novel genes have been shown to play a major role in helminth adaptation to a parasitic lifestyle because they provide the novelty necessary for adaptation to a changing environment, such as living in multiple hosts. Here we present the de novo sequenced and annotated genome of the parasitic trematode Atriophallophorus winterbourni and its comparative genomic analysis to other major parasitic trematodes. First, we reconstructed the species phylogeny, and dated the split of A. winterbourni from the Opisthorchiata suborder to approximately 237.4 Ma (±120.4 Myr). We then addressed the question of which expanded gene families and gained genes are potentially involved in adaptation to parasitism. To do this, we used hierarchical orthologous groups to reconstruct three ancestral genomes on the phylogeny leading to A. winterbourni and performed a GO (Gene Ontology) enrichment analysis of the gene composition of each ancestral genome, allowing us to characterize the subsequent genomic changes. Out of the 11,499 genes in the A. winterbourni genome, as much as 24% have arisen through duplication events since the speciation of A. winterbourni from the Opisthorchiata, and as much as 31.9% appear to be novel, that is, newly acquired. We found 13 gene families in A. winterbourni to have had more than ten genes arising through these recent duplications; all of which have functions potentially relating to host behavioral manipulation, host tissue penetration, and hiding from host immunity through antigen presentation. We identified several families with genes evolving under positive selection. Our results provide a valuable resource for future studies on the genomic basis of adaptation to parasitism and point to specific candidate genes putatively involved in antagonistic host-parasite adaptation.

Indexed as

Gene DuplicationParasitesAdaptation, PhysiologicalAnimalsGene OntologyGenomeGenome SizeGenomicsPhylogenySnailsTrematodacomparative genomicsevolutionphylogenyselection

Identifiers

PMID33484570
PMCPMC7936022
OpenAlexW3124380008

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.