Platelet-derived biomaterial controls aspergillus fumigatus keratitis by decreasing fungal burden: an in vivo study.


Journal

Archives of microbiology
ISSN: 1432-072X
Titre abrégé: Arch Microbiol
Pays: Germany
ID NLM: 0410427

Informations de publication

Date de publication:
20 Jul 2024
Historique:
received: 14 05 2024
accepted: 15 07 2024
revised: 30 06 2024
medline: 21 7 2024
pubmed: 21 7 2024
entrez: 20 7 2024
Statut: epublish

Résumé

Fungal keratitis is a severe corneal infection characterized by suppurative and ulcerative lesions. Aspergillus fumigatus is a common cause of fungal keratitis. Antifungal drugs, such as natamycin, are currently the first-line treatment for fungal keratitis, but their ineffectiveness leads to blindness and perforation. Additionally, the development of fungal resistance makes treating fungal keratitis significantly more challenging. The present study used platelet-derived biomaterial (PDB) to manage A. fumigatus keratitis in the animal model. Freezing and thawing processes were used to prepare PDB, and then A. fumigatus keratitis was induced in the mice. Topical administration of PDB, natamycin, and plasma was performed; quantitative real-time PCR (qPCR) and histopathologic examination (HE) were used to assess the inhibitory effect of the mentioned compounds against fungal keratitis. The qPCR results showed that PDB significantly decreased the count of A. fumigatus compared to the control group (P-value ≤ 5). Natamycin also remarkably reduced the count of fungi in comparison to the untreated animal, but its inhibitory effect was not better than PDB (P-value > 5). The findings of HE also demonstrated that treatment with PDB and natamycin decreased the fungal loads in the corneal tissue. However, plasma did not show a significant inhibitory effect against A. fumigatus. PDB is intrinsically safe and free of any infections or allergic responses; additionally, this compound has a potential role in decreasing the burden of A. fumigatus and treating fungal keratitis. Therefore, scientists should consider PDB an applicable approach to managing fungal keratitis and an alternative to conventional antifungal agents.

Identifiants

pubmed: 39033220
doi: 10.1007/s00203-024-04084-3
pii: 10.1007/s00203-024-04084-3
doi:

Substances chimiques

Antifungal Agents 0
Biocompatible Materials 0
Natamycin 8O0C852CPO

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

358

Subventions

Organisme : Khomein University of Medical Sciences
ID : 4556

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Alireza Moradabadi (A)

Molecular and Medicine Research Center, Khomein University of Medical Sciences, Khomein, Iran.

Abbas Farahani (A)

Molecular and Medicine Research Center, Khomein University of Medical Sciences, Khomein, Iran.
Department of Medical Laboratory Sciences, Khomein University of Medical Sciences, Khomein, Iran.

Zahra Chegini (Z)

Department of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Mohadeseh Hajian (M)

Infectious Diseases Research Center (IDRC), Arak University of Medical Sciences, Arak, Iran.

Reza Hajihossein (R)

Department of Medical Parasitology and Mycology, Arak University of Medical Sciences, Arak, Iran.

Elham Rajaei (E)

Department of Internal Medicine, School of Medicine, Golestan Hospital, Ahvaz Jundishapur University of Medical Science, Ahvaz, Iran.

Mojtaba Didehdar (M)

Department of Medical Parasitology and Mycology, Arak University of Medical Sciences, Arak, Iran. didehdar_m@yahoo.com.
Molecular and Medicine Research Center, Arak University of Medical Sciences, Arak, Iran. didehdar_m@yahoo.com.

Aref Shariati (A)

Infectious Diseases Research Center (IDRC), Arak University of Medical Sciences, Arak, Iran. arefshariati0111@gmail.com.

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