Evidence map›Paper›PMID 25190251›Full record

ReviewCold Spring Harbor perspectives in medicine2014

Metabolism in fungal pathogenesis.

Iuliana V Ene, Sascha Brunke, Alistair J P Brown, Bernhard Hube

Abstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing 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

90 citing papers in PubMed.

  1. Article
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  5. Voriconazole Activity AgainstMolecules (Basel, Switzerland) · 2026
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  8. Article
  9. Review
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  12. Review
  13. Article
  14. Article
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  17. Fungal diversity isolated from the gastrointestinal tract of psittacines kept as pets: a potential public health risk?Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
    Article
  18. Article
  19. Article
  20. Article

30 more citing papers are in PubMed but not listed here.

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

4 authors.

Iuliana V EneAberdeen Fungal Group, School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, United Kingdom.
Sascha BrunkeDepartment of Microbial Pathogenicity Mechanisms, Hans Knoell Institute, 07745 Jena, Germany.
Alistair J P BrownAberdeen Fungal Group, School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, United Kingdom.
Bernhard HubeDepartment of Microbial Pathogenicity Mechanisms, Hans Knoell Institute, 07745 Jena, Germany Friedrich Schiller University, 07743 Jena, Germany Center for Sepsis Control and Care, Universitätsklinikum Jena, 07747 Jena, Germany.

Funding

Biotechnology and Biological Sciences Research Council BB/C510391/1Biotechnology and Biological Sciences Research Council BB/D009308/1Biotechnology and Biological Sciences Research Council BB/F000111/1Biotechnology and Biological Sciences Research Council BB/F00513X/1Biotechnology and Biological Sciences Research Council BB/F010826/1Biotechnology and Biological Sciences Research Council BB/K017365/1Biotechnology and Biological Sciences Research Council BBS/B/06679European Research Council 249793Wellcome TrustWellcome Trust 080088Wellcome Trust 097377
6 · The paper itself

Abstract

Fungal pathogens must assimilate local nutrients to establish an infection in their mammalian host. We focus on carbon, nitrogen, and micronutrient assimilation mechanisms, discussing how these influence host-fungus interactions during infection. We highlight several emerging trends based on the available data. First, the perturbation of carbon, nitrogen, or micronutrient assimilation attenuates fungal pathogenicity. Second, the contrasting evolutionary pressures exerted on facultative versus obligatory pathogens have led to contemporary pathogenic fungal species that display differing degrees of metabolic flexibility. The evolutionarily ancient metabolic pathways are conserved in most fungal pathogen, but interesting gaps exist in some species (e.g., Candida glabrata). Third, metabolic flexibility is generally essential for fungal pathogenicity, and in particular, for the adaptation to contrasting host microenvironments such as the gastrointestinal tract, mucosal surfaces, bloodstream, and internal organs. Fourth, this metabolic flexibility relies on complex regulatory networks, some of which are conserved across lineages, whereas others have undergone significant evolutionary rewiring. Fifth, metabolic adaptation affects fungal susceptibility to antifungal drugs and also presents exciting opportunities for the development of novel therapies.

Indexed as

CandidiasisCarbonFungiHost-Pathogen InteractionsHumansIronMicronutrientsMycosesNitrogenVirulence FactorsZincCarbonIronMicronutrientsNitrogenVirulence FactorsZinc

Identifiers

PMID25190251
PMCPMC4292087

What Socratic holds

Textmetadata
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 Socratic graph.