Inhibition of Melanization by Kojic Acid Promotes Cell Wall Disruption of the Human Pathogenic Fungus Fonsecaea sp.
Jorge Augusto Leão PereiraLienne Silveira de MoraesChubert Bernardo Castro de SenaJosé Luiz Martins do NascimentoAna Paula Drummond RodriguesSilvia Helena Marques da SilvaEdilene Oliveira da SilvaPublished in: Pathogens (Basel, Switzerland) (2022)
Chromoblastomycosis (CBM) is a chronic human subcutaneous mycosis caused by various aetiologic agents. CBM does not have an established treatment but may be managed using antifungal agents, surgical removal of the lesions, or cryotherapy. Kojic acid (KA), a known tyrosinase inhibitor with a variety of biological actions, including fungistatic action against the fungus Cryptococcus neoformans, mediated by inhibiting melanin production, seems to be an alternative to improve the treatment of CBM. The aim of the present study was to analyze the action of KA against the pathogenic fungus Fonsecaea sp., an aetiological agent of CBM. The fungal culture was incubated with KA, and the amount of melanin was assessed, followed by cytochemical detection. Subsequently, the samples were analyzed by light microscopy, transmission and scanning electron microscopy. Culture analysis revealed that 100 g/mL KA significantly decreased the melanization of the fungus and the exocytosis of melanin into the culture supernatant. Additionally, KA induced less growth of biofilm formation and intense disruption of the cell wall, and decreased the number of melanin-containing vesicles in the culture supernatant. Finally, KA inhibited fungal filamentation in culture and the subsequent phagocytosis process. Thus, KA may be a promising substance to help in the treatment of CBM.
Keyphrases
- cell wall
- biofilm formation
- candida albicans
- endothelial cells
- electron microscopy
- pseudomonas aeruginosa
- high resolution
- escherichia coli
- signaling pathway
- cell free
- mass spectrometry
- high throughput
- single cell
- cystic fibrosis
- drug induced
- combination therapy
- label free
- induced pluripotent stem cells
- diabetic rats
- high speed