4.6 Article

Silver Nanoparticles Biosynthesized with Spruce Bark Extract-A Molecular Aggregate with Antifungal Activity against Candida Species

Journal

ANTIBIOTICS-BASEL
Volume 10, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics10101261

Keywords

biosynthesis; biofilm; silver nanoparticles; spruce bark; synergism; SAP2; ALS3; HSP70

Funding

  1. George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, Research Grant [294/5/14.1.2020]

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The study found that silver nanoparticles synthesized using spruce bark exhibit antifungal activity, synergistic effects with fluconazole, and inhibitory effects on biofilm production by Candida species. The silver nanoparticles mediated by spruce bark extract and silver salts could potentially be used as treatment or adjuvant options against not only common Candida albicans but also more aggressive non-albicans Candida species.
Due to their high content of biomolecules, combined with silver's well known antimicrobial potential, silver nanoparticles biosynthesized using spruce bark (AgNP SBEs) demonstrate antibacterial and antioxidant activity, making them a versatile option for developing new antimicrobial agents that might be used for medical treatment or as adjuvants for the classical agents. This study aims to analyze if silver nanoparticles (AgNPs) mediated by spruce bark extract (SBE) and silver salts (AgNP SBE Acetate, AgNP SBE Nitrate) presents antifungal activity against five different Candida spp., synergistic activity with fluconazole, and if they interact with some virulence factors of C. albicans. AgNP SBEs presented MICs (minimum inhibitory concentrations) for all the five tested Candida spp. AgNP SBEs inhibited the growth of C. parapsilosis, C. krusei, and C. guilliermondii, exerted synergistic activity with fluconazole for C. parapsilosis and C. guilliermondii, and inhibited biofilm production for C. albicans, C. auris, and C. guilliermondii. MICs of AgNP SBE Acetate significantly inhibited the production of germ tubes of C. albicans. The expression of C. albicans SAP2 gene was down-regulated by the short-time treatment with MICs of AgNP SBE Acetate, while ALS3 and HSP70 genes were up-regulated by the AgNPs MICs. These results emphasize the potential of using the AgNP SBEs as treatments/adjuvants options, not only against the redundant C. albicans but also for the non-albicans Candida species (which are not as frequently involved in human pathologies, but, sometimes, can be more aggressive).

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