Particle-cell contact enhances antibacterial activity of silver nanoparticles

PLoS One. 2013 May 30;8(5):e64060. doi: 10.1371/journal.pone.0064060. Print 2013.

Abstract

Background: It is generally accepted that antibacterial properties of Ag nanoparticles (AgNPs) are dictated by their dissolved fraction. However, dissolution-based concept alone does not fully explain the toxic potency of nanoparticulate silver compared to silver ions.

Methodology/principal findings: Herein, we demonstrated that the direct contact between bacterial cell and AgNPs' surface enhanced the toxicity of nanosilver. More specifically, cell-NP contact increased the cellular uptake of particle-associated Ag ions - the single and ultimate cause of toxicity. To prove that, we evaluated the toxicity of three different AgNPs (uncoated, PVP-coated and protein-coated) to six bacterial strains: Gram-negative Escherichia coli, Pseudomonas fluorescens, P. putida and P. aeruginosa and Gram-positive Bacillus subtilis and Staphylococcus aureus. While the toxicity of AgNO3 to these bacteria varied only slightly (the 4-h EC50 ranged from 0.3 to 1.2 mg Ag/l), the 4-h EC50 values of protein-coated AgNPs for various bacterial strains differed remarkably, from 0.35 to 46 mg Ag/l. By systematically comparing the intracellular and extracellular free Ag(+) liberated from AgNPs, we demonstrated that not only extracellular dissolution in the bacterial test environment but also additional dissolution taking place at the particle-cell interface played an essential role in antibacterial action of AgNPs. The role of the NP-cell contact in dictating the antibacterial activity of Ag-NPs was additionally proven by the following observations: (i) separation of bacterial cells from AgNPs by particle-impermeable membrane (cut-off 20 kDa, ∼4 nm) significantly reduced the toxicity of AgNPs and (ii) P. aeruginosa cells which tended to attach onto AgNPs, exhibited the highest sensitivity to all forms of nanoparticulate Ag.

Conclusions/significance: Our findings provide new insights into the mode of antibacterial action of nanosilver and explain some discrepancies in this field, showing that "Ag-ion" and "particle-specific" mechanisms are not controversial but, rather, are two faces of the same coin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology
  • Biological Availability
  • Cell Adhesion
  • Chemical Precipitation
  • Dose-Response Relationship, Drug
  • Gram-Negative Bacteria / cytology*
  • Gram-Negative Bacteria / drug effects*
  • Gram-Positive Bacteria / cytology*
  • Gram-Positive Bacteria / drug effects*
  • Intracellular Space / drug effects
  • Metal Nanoparticles*
  • Silver / chemistry*
  • Silver / pharmacology*
  • Silver Compounds / chemistry
  • Silver Compounds / pharmacology
  • Silver Nitrate / chemistry
  • Silver Nitrate / pharmacology
  • Species Specificity

Substances

  • Anti-Bacterial Agents
  • Silver Compounds
  • Silver
  • collargol
  • Silver Nitrate

Grants and funding

This research was supported by the Estonian target funding project SF0690063s08, ETF8561 and ETF9347 grants, European Social Fund and EU 7th Framework Programme under grant agreement no. 263147 (NanoValid). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.