Evidence map›Paper›PMID 27193346›Full record

ReviewCurrent genetics2017

Persistence and drug tolerance in pathogenic yeast.

Rasmus Bojsen, Birgitte Regenberg, Anders Folkesson

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Current genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Low-level direct currents eradicate multi-drug-resistantChemical engineering journal (Lausanne, Switzerland : 1996) · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Unveiling drug-tolerant and persister-like cells inFrontiers in cellular and infection microbiology · 2023
    Article
  9. Quiescence inAnnual review of genetics · 2022
    Review
  10. Fungal biofilm architecture produces hypoxic microenvironments that drive antifungal resistance.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Quiescence, an individual journey.Current genetics · 2019
    Review
  16. Review
  17. Review
  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

3 authors at 2 institutions in 1 country.

Rasmus BojsenNational Veterinary Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
Birgitte RegenbergDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Anders FolkessonNational Veterinary Institute, Technical University of Denmark, Kongens Lyngby, Denmark. afol@vet.dtu.dk.
Technical University of Denmark · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this review, we briefly summarize the current understanding of how fungal pathogens can persist antifungal treatment without heritable resistance mutations by forming tolerant persister cells. Fungal infections tolerant to antifungal treatment have become a major medical problem. One mechanism leading to drug recalcitrance is the formation of antifungal persister cells. These cells have wild-type genotype with the ability to survive exposure to antifungal agents due to changed membrane composition, upregulated stress response, and enhanced cell wall integrity. Knowledge of the mechanisms regulating entry and exit of the persister phenotype is limited, but it has recently been shown that the inhibition of the growth regulating TORC1 pathway induces fungal persistence. The phenotypic properties of persister cells and the involvement of the TORC1 pathway indicate that persister cells are quiescent in G0 of the cell cycle. This knowledge leads us to suggest that the identified shared drug-tolerance mechanisms of persister and quiescent cells may serve as a foundation for developing novel treatment strategies that are independent of growth mode against systemic fungal infections.

Indexed as

Drug Resistance, FungalAdaptation, BiologicalAnimalsAntifungal AgentsCandidiasisCell CycleHost-Pathogen InteractionsHumansMicrobial ViabilityMycosesPhenotypeStress, PhysiologicalYeastsAntifungal AgentsAntifungalPathogenic yeastPersistenceQuiescenceResistanceToleranceTOR

Identifiers

PMID27193346
OpenAlexW2399677191

What OpenQuestion 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 OpenQuestion graph.