Evidence map›Paper›PMID 37143068›Full record

ArticleBMC biology2023

Recent expansion of metabolic versatility in Diplonema papillatum, the model species of a highly speciose group of marine eukaryotes.

Matus Valach, Sandrine Moreira, Celine Petitjean, Corinna Benz, Anzhelika Butenko, Olga Flegontova, Anna Nenarokova, Galina Prokopchuk, Tom Batstone, Pascal Lapébie and 12 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Enzymology of the metazoan tRNA ligase complex: a lifetime in cycles.Cellular and molecular life sciences : CMLS · 2026
    Review
  3. Article
  4. Genetic Manipulation of Paradiplonema papillatum.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  5. Preparation of Diplonemid Samples for Microscopy.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Why Euglenozoans.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  7. Assembly and Annotation of Kinetoplastid and Diplonemid Mitochondrial Genomes.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Biochemistry of Diplonemids.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  9. Isolation and Cultivation of Diplonemids.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  10. Nuclear Genome Assembly and Annotation of Kinetoplastids.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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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

22 authors at 11 institutions in 8 countries.

Matus ValachDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada. matus.a.valach@gmail.com.ORCID 0000-0001-8689-0080
Sandrine MoreiraDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada.ORCID 0000-0002-4580-3566
Celine PetitjeanSchool of Biological Sciences, University of Bristol, Bristol, UK.
Corinna BenzInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID 0000-0003-4367-2758
Anzhelika ButenkoInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID 0000-0001-8685-2404
Olga FlegontovaInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.
Anna NenarokovaSchool of Biological Sciences, University of Bristol, Bristol, UK.ORCID 0000-0003-1441-037X
Galina ProkopchukInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID 0000-0002-7623-5354
Tom BatstoneSchool of Biological Sciences, University of Bristol, Bristol, UK.
Pascal LapébieArchitecture et Fonction des Macromolécules Biologiques (AFMB), CNRS, Aix Marseille Université, Marseille, France.ORCID 0000-0003-4073-0633
Lionnel LemogoDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada.ORCID 0009-0001-4230-7671
Matt SarrasinDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada.ORCID 0000-0003-4849-0849
Paul StretenowichDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada.ORCID 0000-0003-1631-6512
Pragya TripathiInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID 0000-0002-3290-6275
Euki YazakiRIKEN Interdisciplinary Theoretical and Mathematical Sciences Program (iTHEMS), Hirosawa, Wako, Saitama, Japan.ORCID 0000-0003-4962-3340
Takeshi NaraLaboratory of Molecular Parasitology, Graduate School of Life Science and Technology, Iryo Sosei University, Iwaki City, Fukushima, Japan.ORCID 0000-0003-4051-9803
Bernard HenrissatArchitecture et Fonction des Macromolécules Biologiques (AFMB), CNRS, Aix Marseille Université, Marseille, France.ORCID 0000-0002-3434-8588
B Franz LangDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada.ORCID 0000-0003-1035-5449
Michael W GrayDepartment of Biochemistry and Molecular Biology, Institute for Comparative Genomics, Dalhousie University, Halifax, NS, Canada.ORCID 0000-0001-7125-2625
Tom A WilliamsSchool of Biological Sciences, University of Bristol, Bristol, UK.ORCID 0000-0003-1072-0223
Julius LukešInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID 0000-0002-0578-6618
Gertraud BurgerDepartment of Biochemistry, Robert-Cedergren Centre for Bioinformatics and Genomics, Université de Montréal, Montreal, QC, Canada. gertraud.burger@umontreal.ca.ORCID 0000-0002-8679-8812
Université de Montréal · CAUniversity of Bristol · GBUniversity of South Bohemia in České Budějovice · CZCentre National de la Recherche Scientifique · FRUniversity of Ostrava · CZDalhousie University · CAEnvironment and Climate Change Canada · CAInstitute of Parasitology · CZIRYO Sosei University · JPMcGill Genome Centre · CARIKEN · JP

Funding

Biotechnology and Biological Sciences Research Council BB/R016437/1
6 · The paper itself

Abstract

backgroundDiplonemid flagellates are among the most abundant and species-rich of known marine microeukaryotes, colonizing all habitats, depths, and geographic regions of the world ocean. However, little is known about their genomes, biology, and ecological role.

resultsWe present the first nuclear genome sequence from a diplonemid, the type species Diplonema papillatum. The ~ 280-Mb genome assembly contains about 32,000 protein-coding genes, likely co-transcribed in groups of up to 100. Gene clusters are separated by long repetitive regions that include numerous transposable elements, which also reside within introns. Analysis of gene-family evolution reveals that the last common diplonemid ancestor underwent considerable metabolic expansion. D. papillatum-specific gains of carbohydrate-degradation capability were apparently acquired via horizontal gene transfer. The predicted breakdown of polysaccharides including pectin and xylan is at odds with reports of peptides being the predominant carbon source of this organism. Secretome analysis together with feeding experiments suggest that D. papillatum is predatory, able to degrade cell walls of live microeukaryotes, macroalgae, and water plants, not only for protoplast feeding but also for metabolizing cell-wall carbohydrates as an energy source. The analysis of environmental barcode samples shows that D. papillatum is confined to temperate coastal waters, presumably acting in bioremediation of eutrophication.

conclusionsNuclear genome information will allow systematic functional and cell-biology studies in D. papillatum. It will also serve as a reference for the highly diverse diplonemids and provide a point of comparison for studying gene complement evolution in the sister group of Kinetoplastida, including human-pathogenic taxa.

Indexed as

EukaryotaKinetoplastidaEuglenozoaHumansMeiotic Prophase IMultigene FamilyPhylogenyCAZymesEcological distributionFeeding strategyGene-family evolutionGenomeGeographical distributionLateral gene transferParadiplonema papillatumProteomeProtistsTranscriptome

Identifiers

PMID37143068
PMCPMC10161547
OpenAlexW4368618126

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LicenceCC BY
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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.