Evidence map›Paper›PMID 27075306›Full record

ArticleParasitology research2016

Molecular identification of Nucleophaga terricolae sp. nov. (Rozellomycota), and new insights on the origin of the Microsporidia.

Daniele Corsaro, Rolf Michel, Julia Walochnik, Danielle Venditti, Karl-Dieter Müller, Bärbel Hauröder, Claudia Wylezich

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Article in Parasitology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Frontiers in cellular and infection microbiology · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Gut Microbial Alterations in Diarrheal Baer's Pochards (Frontiers in veterinary science · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Fungal evolution: diversity, taxonomy and phylogeny of the Fungi.Biological reviews of the Cambridge Philosophical Society · 2019
    Article
  16. Fungal evolution: major ecological adaptations and evolutionary transitions.Biological reviews of the Cambridge Philosophical Society · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. Clarifying the Relationships between Microsporidia and Cryptomycota.The Journal of eukaryotic microbiology · 2018
    Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Daniele CorsaroCHLAREAS Chlamydia Research Association Nancy, 12 rue du Maconnais, F-54500, Vandoeuvre-lès-Nancy, France. corsaro@gmx.fr.
Rolf MichelCentral Institute of the Federal Armed Forces Medical Services, P.O. Box 7340, 56070, Koblenz, Germany.
Julia WalochnikMolecular Parasitology, Institute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Kinderspitalgasse 15, 1095, Vienna, Austria.
Danielle VendittiCHLAREAS Chlamydia Research Association Nancy, 12 rue du Maconnais, F-54500, Vandoeuvre-lès-Nancy, France.
Karl-Dieter MüllerInstitut of Medical Microbiology, University of Duisburg-Essen, Virchowstr.179, 45147, Essen, Germany.
Bärbel HauröderCentral Institute of the Federal Armed Forces Medical Services, P.O. Box 7340, 56070, Koblenz, Germany.
Claudia WylezichIOW-Leibniz-Institute for Baltic Sea Research Warnemünde, Seestr. 15, Rostock, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microsporidia are widespread endoparasites of animals, including humans. They are characterized by highly modified morphological and genetic features that cause difficulties in elucidating their enigmatic origin and evolution. Recent advances, however, indicate that the Microsporidia have emerged from the Rozellomycota, forming together either the most basal lineage of the Fungi or its closer relative. The Rozellomycota comprise a huge diversity of uncultured environmental clones, with a very few known species endoparasitic of algae and water moulds, like the chytrid-like Rozella, and of free-living amoebae, like Nucleophaga and the microsporidia-like Paramicrosporidium. A possible ancestral microsporidium, Mitosporidium, has recently been described from the water flea Daphnia, since the phylogenomic reconstruction showed that it branches to the root of the microsporidian tree, while the genome analysis revealed a fungal-like nuclear genome and the persistence of a mitochondrial genome. Here we report the 18S rDNA molecular phylogeny of an additional microsporidium-like endoparasite of amoebae, which has a developmental cycle almost identical to that of Nucleophaga amoebae. Our results show that the endoparasite is closely related to N. amoebae, forming a distinct species, for which we propose the name Nucleophaga terricolae. Furthermore, the Nucleophaga lineage is recovered as sister to the Microsporidia while Mitosporidium turns out to be member of a well-supported group of environmental clones. These results raise the question about the actual ancestry of the Microsporidia within the Rozellomycota. A precise and robust phylogeny will require further comparative genomic studies of these various strains, and should also consider the primitive microsporidia, for which genetic data are still lacking, because all these organisms are essentially morphologically similar.

Indexed as

Biological EvolutionAmoebaAnimalsDaphniaDNA, RibosomalEvolution, MolecularGenomicsMicrosporidia, UnclassifiedPhylogenyRNA, Ribosomal, 18SDNA, RibosomalRNA, Ribosomal, 18SAmoebaeEndoparasiteMicrosporidiaNucleophagaRozellomycota

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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.