Evidence map›Paper›PMID 40595376›Full record

ArticleScientific reports2025

Yeast-derived glycolipids disrupt Candida biofilm and inhibit expression of genes in cell adhesion.

Kwanrutai Watchaputi, Pattanan Songdech, Channa Jayasekara, Panupong Puttarak, Erwin Lamping, Richard D Cannon, Nitnipa Soontorngun

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A Glycolipid-Like Biosurfactant Molecule Derived From anInternational journal of microbiology · 2026
    Article
  5. Review
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

7 authors.

Kwanrutai WatchaputiExcellent Research Laboratory for Yeast Innovation, Division of Biochemical Technology, School of Bioresources and Technology, King Mongkut's University of Technology Thonburi (KMUTT), Bangkok, 10150, Thailand.
Pattanan SongdechExcellent Research Laboratory for Yeast Innovation, Division of Biochemical Technology, School of Bioresources and Technology, King Mongkut's University of Technology Thonburi (KMUTT), Bangkok, 10150, Thailand.
Channa JayasekaraExcellent Research Laboratory for Yeast Innovation, Division of Biochemical Technology, School of Bioresources and Technology, King Mongkut's University of Technology Thonburi (KMUTT), Bangkok, 10150, Thailand.
Panupong PuttarakPhytomedicine and Pharmaceutical Biotechnology Excellence Center, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat-Yai, 90110, Songkhla, Thailand.
Erwin LampingSir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.
Richard D CannonSir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.
Nitnipa SoontorngunExcellent Research Laboratory for Yeast Innovation, Division of Biochemical Technology, School of Bioresources and Technology, King Mongkut's University of Technology Thonburi (KMUTT), Bangkok, 10150, Thailand. nitnipa.soo@kmutt.ac.th.

Funding

Excellent Research Laboratory for Yeast Innovation of Fiscal Year 2023 6620864King Mongkut's university of Technology Thonburi: KMUTT partnering initiative grant fiscal year 2023 under KIRIM 27802King Mongkut's University of Technology Thonburi's Postdoctoral Fellowship in fiscal year 2024 under KIRIM Research Project 28074National Research Council of Thailand (NRCT) and King Mongkut's University of Technology Thonburi for Mid-Career Researcher grant N42A650315
6 · The paper itself

Abstract

Candida albicans is a leading fungal pathogen in humans, responsible for infections that span from mucosal surfaces to severe systemic diseases. This study aimed to investigate potential ability of yeast-derived glycolipids from Meyerozyma guilliermondii as an antifungal against Candida albicans biofilms. Glycolipid extract (64 µg/mL) reduced metabolic activity by 50% in both immature and mature biofilms, while biofilm mass was reduced at higher concentrations of 128 and 256 µg/mL, respectively. Adhesion, a key step in biofilm formation, decreased by over 50% when cells were treated with glycolipids (16 µg/mL). Gene expression analysis indicated that glycolipids downregulated key adhesion-related gene ACE2, confirming their role in disrupting C. albicans adhesion. Importantly, structural changes in C. albicans biofilms, including reduced hyphal production and wrinkled cell surfaces, were observed under SEM. Nocodazole, a cell cycle synchronizer, arrested cells in the G

Indexed as

Antifungal AgentsBiofilmsCandida albicansCell AdhesionGene Expression Regulation, FungalGlycolipidsHumansAntifungal AgentsGlycolipidsAntifungalsAnti-inflammatoryBiosurfactantCandida albicansCell cycleDrug resistance

Identifiers

PMID40595376
PMCPMC12218386

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.