Evidence map›Paper›PMID 33323978›Full record

ArticleThe ISME journal2021

Metabolic modeling predicts specific gut bacteria as key determinants for Candida albicans colonization levels.

Mohammad H Mirhakkak, Sascha Schäuble, Tilman E Klassert, Sascha Brunke, Philipp Brandt, Daniel Loos, Ruben V Uribe, Felipe Senne de Oliveira Lino, Yueqiong Ni, Slavena Vylkova and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. microLife · 2026
    Article
  3. Article
  4. Article
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  6. Article
  7. Review
  8. Article
  9. Review
  10. [The intestinal microbiota in inflammatory bowel diseases].Innere Medizin (Heidelberg, Germany) · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Metabolic modeling of host-microbe interactions.Computational and structural biotechnology journal · 2025
    Review
  15. Article
  16. Article
  17. A mouse model of immunosuppression facilitates oralFrontiers in cellular and infection microbiology · 2024
    Article
  18. Review
  19. Article
  20. 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 at 4 institutions in 3 countries.

Mohammad H Mirhakkak *Systems Biology & Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.
Sascha Schäuble *Systems Biology & Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.ORCID http://orcid.org/0000-0003-3862-6546
Tilman E KlassertZIK Septomics, Jena University Hospital, 07745, Jena, Germany.
Sascha BrunkeDepartment of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.
Philipp BrandtSeptomics Research Center, Friedrich Schiller University, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.
Daniel LoosSystems Biology & Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.ORCID http://orcid.org/0000-0002-4024-4443
Ruben V UribeNovo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800, Kgs. Lyngby, Denmark.
Felipe Senne de Oliveira LinoNovo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800, Kgs. Lyngby, Denmark.
Yueqiong NiSystems Biology & Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.
Slavena VylkovaSeptomics Research Center, Friedrich Schiller University, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.
Hortense SlevogtZIK Septomics, Jena University Hospital, 07745, Jena, Germany.
Bernhard HubeDepartment of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany.
Glen J WeissMiRanostics Consulting, 85755, Oro Valley, AZ, USA.
Morten O A SommerNovo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800, Kgs. Lyngby, Denmark.ORCID http://orcid.org/0000-0003-4005-5674
Gianni PanagiotouSystems Biology & Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, 07745, Jena, Germany. Gianni.Panagiotou@leibniz-hki.de.ORCID http://orcid.org/0000-0001-9393-124X
Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) · DENovo Nordisk Foundation · DKJena University Hospital · DEMolecular Theranostics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Candida albicans is a leading cause of life-threatening hospital-acquired infections and can lead to Candidemia with sepsis-like symptoms and high mortality rates. We reconstructed a genome-scale C. albicans metabolic model to investigate bacterial-fungal metabolic interactions in the gut as determinants of fungal abundance. We optimized the predictive capacity of our model using wild type and mutant C. albicans growth data and used it for in silico metabolic interaction predictions. Our analysis of more than 900 paired fungal-bacterial metabolic models predicted key gut bacterial species modulating C. albicans colonization levels. Among the studied microbes, Alistipes putredinis was predicted to negatively affect C. albicans levels. We confirmed these findings by metagenomic sequencing of stool samples from 24 human subjects and by fungal growth experiments in bacterial spent media. Furthermore, our pairwise simulations guided us to specific metabolites with promoting or inhibitory effect to the fungus when exposed in defined media under carbon and nitrogen limitation. Our study demonstrates that in silico metabolic prediction can lead to the identification of gut microbiome features that can significantly affect potentially harmful levels of C. albicans.

Indexed as

Candida albicansGastrointestinal MicrobiomeBacteriaBacteroidetesHumansMetagenomics

Identifiers

PMID33323978
PMCPMC8115155
OpenAlexW3112425271

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.