4.6 Article

Toxicity of differently sized and charged silver nanoparticles to yeast Saccharomyces cerevisiae BY4741: a nano-biointeraction perspective

Journal

NANOTOXICOLOGY
Volume 13, Issue 8, Pages 1041-1059

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/17435390.2019.1621401

Keywords

Silver nanoparticles; toxicity; cell structure; confocal and electron microscopy

Funding

  1. Estonian Research Council [IUT 23-5, ETF9001]
  2. Fondazione Cariplo [2013-0987]
  3. ERDF project 'Centre of Technologies and Investigations of Nanomaterials (NAMURthorn)' [2014-2020.4.01.16-0123]
  4. 'Center of Excellence' project TK134 'Emerging orders in quantum and nanomaterials'
  5. EU COST Action [ES1205]

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In the current study, we evaluated the modulatory effects of size and surface coating/charge of AgNPs on their toxicity to a unicellular yeast Saccharomyces cerevisiae BY4741 - a fungal model. For that, the toxicity of a set of 10 and 80 nm citrate-coated (negatively charged) and branched polyethylenimine (bPEI) coated (positively charged) AgNPs was evaluated in parallel with AgNO3 as ionic control. Yeast cells were exposed to different concentrations of studied compounds in deionized water for 24 h at 30 degrees C and evaluated for the viability by the post-exposure colony-forming ability. Particle-cell interactions were assessed by SEM, TEM and confocal laser scanning microscopy (CLSM) in the reflection mode. AgNPs toxicity to yeast was size and charge-dependent: 24-h IC50 values ranged from 0.04 (10nAg-bPEI) up to 8.3 mg Ag/L (80nAg-Cit). 10 nm AgNPs were 5-27 times more toxic than 80 nm AgNPs and bPEI-AgNPs 8-44 times more toxic than citrate-AgNPs. SEM and TEM visualization showed that bPEI-AgNPs but not citrate-AgNPs adsorbed onto the yeast cell's surface. However, according to CLSM all the studied AgNPs, whatever the size and coating, ended up within the yeast cell. Toxicity of citrate-AgNPs was largely explained by the dissolved Ag ions but the bPEI-AgNPs showed mainly particle-driven effects leading to the cellular internalization and/or to more pronounced dissolution of AgNPs in the close vicinity of the cell wall. Therefore, the size, and especially the coating/charge of AgNPs can be efficiently used for the design of new more efficient antifungals.

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