Evidence map›Paper›PMID 40998980›Full record

ArticleNature microbiology2025

Dynamic expression of candidalysin facilitates oral colonization of Candida albicans in mice.

Ricardo Fróis-Martins, Julia Lagler, Tim B Schille, Osama Elshafee, Kontxi Martinez de San Vicente, Sarah Mertens, Michelle Stokmaier, Iman Kilb, Natacha Sertour, Sophie Bachellier-Bassi and 5 more

Abstract read
In one paragraph

Article in Nature microbiology, 2025. 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
–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

13 citing papers in PubMed.

  1. Article
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  10. The pathogenicity and future treatment strategies ofFrontiers in cellular and infection microbiology · 2026
    Review
  11. Review
  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

15 authors.

Ricardo Fróis-MartinsSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.ORCID http://orcid.org/0000-0002-7338-2383
Julia LaglerSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Tim B SchilleDepartment of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute (HKI), Jena, Germany.ORCID http://orcid.org/0009-0008-8296-5434
Osama ElshafeeDepartment of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute (HKI), Jena, Germany.
Kontxi Martinez de San VicenteSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.ORCID http://orcid.org/0000-0003-3320-7035
Sarah MertensSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Michelle StokmaierSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Iman KilbSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Natacha SertourInstitut Pasteur, Université Paris Cité, INRAE USC2019, Unité Biologie et Pathogénicité Fongiques, Paris, France.
Sophie Bachellier-BassiInstitut Pasteur, Université Paris Cité, INRAE USC2019, Unité Biologie et Pathogénicité Fongiques, Paris, France.ORCID http://orcid.org/0000-0003-3970-4825
Selene MogaveroDepartment of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute (HKI), Jena, Germany.ORCID http://orcid.org/0000-0003-0642-0068
Dominique SanglardInstitute of Microbiology, University of Lausanne and University Hospital Center, Lausanne, Switzerland.ORCID http://orcid.org/0000-0002-5244-4178
Christophe d'EnfertInstitut Pasteur, Université Paris Cité, INRAE USC2019, Unité Biologie et Pathogénicité Fongiques, Paris, France.ORCID http://orcid.org/0000-0002-6235-3886
Bernhard HubeDepartment of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute (HKI), Jena, Germany. bernhard.hube@leibniz-hki.de.ORCID http://orcid.org/0000-0002-6028-0425
Salomé LeibundGut-LandmannSection of Immunology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland. salome.leibundgut-landmann@uzh.ch.ORCID http://orcid.org/0000-0002-5724-4837

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 390713860EC | EC Seventh Framework Programm | FP7 People: Marie-Curie Actions (FP7-PEOPLE - Specific Programme "People" Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013)) 812969Novartis Stiftung für Medizinisch-Biologische Forschung (Novartis Foundation for Medical-Biological Research) 22C224Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) CRSII5_173863Uniscientia Stiftung 206-2023
6 · The paper itself

Abstract

Candida albicans is a common fungal member of the human microbiota but can also cause infections via expression of virulence factors associated with the yeast-to-hyphae transition. The evolutionary selection pressure to retain these pathogenic traits for a commensal microorganism remains unclear. Here we show that filamentation and hyphae-associated factors, including the toxin candidalysin, are crucial for colonization of the oral cavity, a major reservoir of C. albicans. Low-virulent strains of C. albicans expressed the candidalysin-encoding gene ECE1 transiently upon exposure to keratinocytes in vitro. In mice, ECE1 mutants were defective at accessing terminally differentiated oral epithelial layers where the fungus is protected from IL-17-mediated immune defence. Tight regulation of ECE1 expression prevented detrimental effects of candidalysin on the host. Our results suggest that hyphae-associated factors such as candidalysin govern not only pathogenicity, but also mucosal colonization through direct host interactions enabling C. albicans to create and maintain its niche in the oral mucosa.

Indexed as

Candida albicansCandidiasis, OralFungal ProteinsMouthAnimalsFemaleGene Expression Regulation, FungalHost-Pathogen InteractionsHumansHyphaeInterleukin-17KeratinocytesMiceMice, Inbred C57BLMouth MucosaVirulenceECE1 protein, Candida albicansFungal ProteinsInterleukin-17Virulence Factors

Identifiers

PMID40998980
PMCPMC12488495

What OpenQuestion holds

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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.