Evidence map›Paper›PMID 42296143›Full record

ArticlePLoS computational biology2026

Fung-AI: An AI/ML-driven pipeline for antifungal peptide discovery.

Daniel S Berman, Libby M Lewis, Tom D Curtis, Olivia N Tiburzi, Daniel F Q Smith, Arturo Casadevall, Laura J Dunphy

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Daniel S BermanJohns Hopkins Applied Physics Laboratory, Laurel, Maryland, United States of America.ORCID https://orcid.org/0000-0002-9176-7535
Libby M LewisJohns Hopkins Applied Physics Laboratory, Laurel, Maryland, United States of America.ORCID https://orcid.org/0000-0001-6520-5988
Tom D CurtisJohns Hopkins Applied Physics Laboratory, Laurel, Maryland, United States of America.
Olivia N TiburziJohns Hopkins Applied Physics Laboratory, Laurel, Maryland, United States of America.
Daniel F Q SmithW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Arturo CasadevallW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Laura J DunphyJohns Hopkins Applied Physics Laboratory, Laurel, Maryland, United States of America.ORCID https://orcid.org/0000-0003-1797-8403

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging fungal pathogens represent a concerning threat to both global health and food security. In this study, we aimed to address our rising vulnerability to fungal pathogens through the development of the Fung-AI pipeline: an AI/ML-driven approach for antifungal discovery. A generative adversarial network (GAN) was trained to generate novel candidate antifungal peptide sequences. Next, in silico antifungal and hemolytic classifiers were built to further prioritize AI-generated peptides for experimental validation. From a pool of ~10,000 candidates, thirteen peptides were selected for testing over two-stages of experimentation. Five peptides were found to display mild antifungal activity against the wheat pathogen, Fusarium graminearum, with minimal inhibitory concentrations (MICs) ranging from 250 µg/mL to 500 µg/mL. Four of the five peptides also showed activity against the human pathogen, Candida albicans (MIC: 500 µg/mL). Two of our AI-generated antifungal peptides additionally demonstrated low cytotoxicity in HepG2 human liver carcinoma cells (LC50 > 704.2 µg/mL) indicating that they may be useful as scaffolds for future optimization for therapeutic applications. None of our peptides were found to considerably inhibit the emerging pathogen C. auris, suggesting the need for pathogen-specific down-selection of candidate peptides. Overall, we present a proof-of-principle, generative-AI-based approach for the rapid design of de novo antifungal peptides.

Indexed as

Antifungal AgentsArtificial IntelligenceDrug DiscoveryPeptidesCandida albicansComputational BiologyFusariumGenerative Adversarial NetworksGenerative Artificial IntelligenceHep G2 CellsHumansMicrobial Sensitivity TestsAntifungal AgentsPeptides

Identifiers

PMID42296143
PMCPMC13289945

What OpenQuestion holds

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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.