In vitro eradication of Fusarium oxysporium conidia using light-triggered thiopyridinium porphyrin-cyclodextrin dyes

The genus Fusarium comprises filamentous fungi widely distributed in soil and plants, representing threats to various organisms, including plants, animals, and humans. Conventional fungicides have limitations, leading to a growing interest in sustainable control methods such as photodynamic inactivation (PDI) of microorganisms. This study evaluates the antifungal photodynamic activity of meso -substituted porphyrin derivatives (H 2 Pors 1a – 3a ), which each structure is composed by three thiopyridinium groups and one cyclodextrin group (α-, β-, or γ-CD). These water-soluble porphyrin-cyclodextrin derivatives were prepared and tested on Fusarium oxysporium conidia. Photoinactivation tests were conducted at different concentrations (1.0, 2.5, and 5.0 μM) under white light exposure at an irradiance of 25 mW.cm − 2 for 60 min (light dose of 90 J.cm − 2 ). Fungal inactivation was observed for all molecules at the highest tested concentration. H 2 Por 3a demonstrated the strongest PDI effect, achieving complete inactivation of the conidia (5.0 log 10 viability reduction) at 2.5 and 5.0 μM and partially at 1.0 μM (~3.0 log 10 viability reduction). H 2 Por 1a showed similar results to H 2 Por 3a at the highest concentration, but was less effective at the lowest concentration. H 2 Por 2a showed partial inactivation of the fungi at the highest tested concentration of 5.0 μM (2 log 10 viability reduction). This lower antifungal activity is attributed to the β-CD forming aggregates in water. These findings suggest that H 2 Pors 1a and 3a are promising drugs for the photoinactivation of F. oxysporium conidia. • Photoinactivation (PDI) of F. oxysporum using substituted porphyrin dyes (H 2 Pors 1a – 3a ). • H 2 Pors 1a – 3a can generate singlet oxygen species under white light irradiation. • High PDI of H 2 Por 3a against F. oxysporum (5.0 log 10 viability reduction, 2.5–5.0 μM, 60 min). • H 2 Por 1a showed similar results to H 2 Por 3a at the concentration of 5.0 μM.

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Publication Details

Journal
Journal of Photochemistry and Photobiology A Chemistry
Published
2025-08-22
DOI
https://doi.org/10.1016/j.jphotochem.2025.116719
Citations
2
Primary Topic
Plant Pathogens and Fungal Diseases
Type
article
Field-Weighted Citation Impact
2.30

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article

In vitro eradication of Fusarium oxysporium conidia using light-triggered thiopyridinium porphyrin-cyclodextrin dyes

Cláudia P.S. Ribeiro, Isabel N. Sierra-García, Leandro M. O. Lourenço, Ângela Cunha
2 citations
Journal of Photochemistry and Photobiology A Chemistry
Plant Pathogens and Fungal Diseases
2.30
article

In vitro eradication of Fusarium oxysporium conidia using light-triggered thiopyridinium porphyrin-cyclodextrin dyes

Cláudia P.S. Ribeiro, Isabel N. Sierra-García, Leandro M. O. Lourenço, Ângela Cunha
article en
2 citations

Abstract

The genus Fusarium comprises filamentous fungi widely distributed in soil and plants, representing threats to various organisms, including plants, animals, and humans. Conventional fungicides have limitations, leading to a growing interest in sustainable control methods such as photodynamic inactivation (PDI) of microorganisms. This study evaluates the antifungal photodynamic activity of meso -substituted porphyrin derivatives (H 2 Pors 1a – 3a ), which each structure is composed by three thiopyridinium groups and one cyclodextrin group (α-, β-, or γ-CD). These water-soluble porphyrin-cyclodextrin derivatives were prepared and tested on Fusarium oxysporium conidia. Photoinactivation tests were conducted at different concentrations (1.0, 2.5, and 5.0 μM) under white light exposure at an irradiance of 25 mW.cm − 2 for 60 min (light dose of 90 J.cm − 2 ). Fungal inactivation was observed for all molecules at the highest tested concentration. H 2 Por 3a demonstrated the strongest PDI effect, achieving complete inactivation of the conidia (5.0 log 10 viability reduction) at 2.5 and 5.0 μM and partially at 1.0 μM (~3.0 log 10 viability reduction). H 2 Por 1a showed similar results to H 2 Por 3a at the highest concentration, but was less effective at the lowest concentration. H 2 Por 2a showed partial inactivation of the fungi at the highest tested concentration of 5.0 μM (2 log 10 viability reduction). This lower antifungal activity is attributed to the β-CD forming aggregates in water. These findings suggest that H 2 Pors 1a and 3a are promising drugs for the photoinactivation of F. oxysporium conidia. • Photoinactivation (PDI) of F. oxysporum using substituted porphyrin dyes (H 2 Pors 1a – 3a ). • H 2 Pors 1a – 3a can generate singlet oxygen species under white light irradiation. • High PDI of H 2 Por 3a against F. oxysporum (5.0 log 10 viability reduction, 2.5–5.0 μM, 60 min). • H 2 Por 1a showed similar results to H 2 Por 3a at the concentration of 5.0 μM.

Journal of Photochemistry and Photobiology A ChemistryVol. 471
University of Lisbon (PT), Rede de Química e Tecnologia (PT), University of Aveiro (PT)
Universidade de Aveiro, Ministério da Ciência, Tecnologia e Ensino Superior, Laboratório Associado para a Química Verde, Centro de Química Estrutural, Centro de Estudos Ambientais e Marinhos, Universidade de Aveiro, Fundação para a Ciência e a Tecnologia, Institute for Molecular Science
Zero hunger
Openalex Percentile: Top 12%
Plant Pathogens and Fungal Diseases
2.30
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