Evidence map›Paper›PMID 27248439›Full record

ReviewVirulence2017

Trehalose pathway as an antifungal target.

John R Perfect, Jennifer L Tenor, Yi Miao, Richard G Brennan

Open access · goldAbstract readReview
In one paragraph

Review in Virulence, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

45 citing papers in PubMed, 78 citations in OpenAlex.

  1. TreC: A Critical Mediator of lysoPC-Induced Hypervirulence inTransboundary and emerging diseases · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Cryptococcal nutrient acquisition and pathogenesis: dining on the host.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  8. Article
  9. Article
  10. Antifungal and anti-biofilm effects of hydrazone derivatives onJournal of enzyme inhibition and medicinal chemistry · 2024
    Article
  11. Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogenProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Review
  13. Article
  14. Frontiers in cellular and infection microbiology · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Metabolite Profile of the Micromycete Lecanicillium gracile Isolated from Plaster and Limestone.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2022
    Article
  20. Virulence · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

John R Perfecta Departments of Medicine and Biochemistry , Duke University Medical Center , Durham , NC , USA.
Jennifer L Tenora Departments of Medicine and Biochemistry , Duke University Medical Center , Durham , NC , USA.
Yi Miaoa Departments of Medicine and Biochemistry , Duke University Medical Center , Durham , NC , USA.
Richard G Brennana Departments of Medicine and Biochemistry , Duke University Medical Center , Durham , NC , USA.
Duke Medical Center · US

Funding

Trehalose Pathway for Antifungal Targets and InhibitorsP01AI104533 · NIAID · DUKE UNIVERSITY · PI PERFECT, JOHN R. · 2015 to 2019
$9.0M
Pathobiology of C. neoformans in the Central Nervous SystemR01AI073896 · NIAID · DUKE UNIVERSITY · PI PERFECT, JOHN R. · 2008 to 2018
$4.4M
Evolution of Cryptococcus neoformans Strains from Patients with HIV/AIDSR01AI093257 · NIAID · DUKE UNIVERSITY · PI PERFECT, JOHN R. · 2011 to 2022
$3.8M
NIAID NIH HHS P01 AI104533NIAID NIH HHS R01 AI073896NIAID NIH HHS R01 AI093257
6 · The paper itself

Abstract

With an increasing immunocompromised population which is linked to invasive fungal infections, it is clear that our present 3 classes of antifungal agents may not be sufficient to provide optimal management to these fragile patients. Furthermore, with widespread use of antifungal agents, drug-resistant fungal infections are on the rise. Therefore, there is some urgency to develop the antifungal pipeline with the goal of new antifungal agent discovery. In this review, a simple metabolic pathway, which forms the disaccharide, trehalose, will be characterized and its potential as a focus for antifungal target(s) explained. It possesses several important features for development of antifungal agents. First, it appears to have fungicidal characteristics and second, it is broad spectrum with importance across both ascomycete and basidiomycete species. Finally, this pathway is not found in mammals so theoretically specific inhibitors of the trehalose pathway and its enzymes in fungi should be relatively non-toxic for mammals. The trehalose pathway and its critical enzymes are now in a position to have directed antifungal discovery initiated in order to find a new class of antifungal drugs.

Indexed as

Drug DiscoveryAnimalsAntifungal AgentsEnzyme InhibitorsFluconazoleFungiGlucosyltransferasesHumansMetabolic Networks and PathwaysMycosesTrehaloseAntifungal AgentsEnzyme InhibitorsFluconazoleGlucosyltransferasesTrehalosetrehalose-6-phosphate synthaseantifungaldrug developmenttrehalose

Identifiers

PMID27248439
PMCPMC5383216
OpenAlexW2424522425

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.