Evidence map›Paper›PMID 42554406›Full record

ArticleInvestigative ophthalmology & visual science2026

Morphological Changes in Fungal Elements and Antifungal Drug Susceptibility in an Ex Vivo Model of Fungal Keratitis.

Tomoko Miyakubo, Takashi Tamura, Aya Komori, Takane Ueda, Noriaki Ishioka, Daisuke Todokoro, Koichi Makimura

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tomoko MiyakuboLaboratory of Medical Mycology, Graduate School of Medicine, Teikyo University, Tokyo, Japan.
Takashi TamuraInstitute of Medical Mycology, Teikyo University, Tokyo, Japan.
Aya KomoriInstitute of Medical Mycology, Teikyo University, Tokyo, Japan.
Takane UedaInstitute of Medical Mycology, Teikyo University, Tokyo, Japan.
Noriaki IshiokaInstitute of Medical Mycology, Teikyo University, Tokyo, Japan.
Daisuke TodokoroDepartment of Ophthalmology, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Koichi MakimuraLaboratory of Medical Mycology, Graduate School of Medicine, Teikyo University, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Fungal keratitis is a serious eye infection that can cause irreversible vision loss. One of the causative fungal pathogens, Fusarium solani (Neocosmospora solani), shows limited susceptibility to antifungal drugs. Furthermore, differences between in vitro and clinical outcomes are encountered in some cases, complicating treatment. In this study, we compared in vitro and ex vivo antifungal susceptibility using a porcine corneal model of F. solani keratitis. Methods: An ex vivo fungal keratitis model was developed using porcine corneas, which were inoculated with F. solani and assigned to four treatment groups: natamycin (NAT), voriconazole (VRCZ), luliconazole (LLCZ), or saline (uninfected control). We compared the antifungal efficacy of each drug on day 2 to day 4 of fungal development. DNA was extracted from all corneas and used in real-time polymerase chain reaction to quantitatively assess fungal growth. Fungal morphology was examined by digital microscopy. Results: All antifungal treatment groups demonstrated antifungal activity. The NAT-treated group showed clear inhibition of fungal growth as well as fungal structural damage. The VRCZ-treated group exhibited growth inhibition; however, fungal growth persisted even after additional drug administration. The LLCZ-treated group not only suppressed fungal growth but also caused structural disruption of fungal cells after additional administration, suggesting a strong antifungal effect. Conclusions: We successfully established an ex vivo Fusarium keratitis model using porcine corneas, which enabled us to evaluate antifungal susceptibility by quantifying fungal growth and observing fungal morphological changes.

Indexed as

Antifungal AgentsCorneaCorneal UlcerEye Infections, FungalFusariosisFusariumKeratitisAnimalsDisease Models, AnimalDNA, FungalDrug Resistance, FungalMicrobial Sensitivity TestsNatamycinReal-Time Polymerase Chain ReactionSwineVoriconazoleAntifungal AgentsDNA, FungalNatamycinVoriconazole

Identifiers

PMID42554406
PMCPMC13450652

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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.