International Journal of Molecular Sciences (May 2021)

Potential of Silver Nanoparticles in Overcoming the Intrinsic Resistance of <i>Pseudomonas aeruginosa</i> to Secondary Metabolites from Carnivorous Plants

  • Marta Krychowiak-Maśnicka,
  • Mirosława Krauze-Baranowska,
  • Sylwia Godlewska,
  • Zbigniew Kaczyński,
  • Aleksandra Bielicka-Giełdoń,
  • Natalia Grzegorczyk,
  • Magdalena Narajczyk,
  • Joanna E. Frackowiak,
  • Aleksandra Krolicka

DOI
https://doi.org/10.3390/ijms22094849
Journal volume & issue
Vol. 22, no. 9
p. 4849

Abstract

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Carnivorous plants are exemplary natural sources of secondary metabolites with biological activity. However, the therapeutic antimicrobial potential of these compounds is limited due to intrinsic resistance of selected bacterial pathogens, among which Pseudomonas aeruginosa represents an extreme example. The objective of the study was to overcome the intrinsic resistance of P. aeruginosa by combining silver nanoparticles (AgNPs) with secondary metabolites from selected carnivorous plant species. We employed the broth microdilution method, the checkerboard titration technique and comprehensive phytochemical analyses to define interactions between nanoparticles and active compounds from carnivorous plants. It has been confirmed that P. aeruginosa is resistant to a broad range of secondary metabolites from carnivorous plants, i.e., naphthoquinones, flavonoids, phenolic acids (MBC = 512 µg mL−1) and only weakly sensitive to their mixtures, i.e., extracts and extracts’ fractions. However, it was shown that the antimicrobial activity of extracts and fractions with a significant level of naphthoquinone (plumbagin) was significantly enhanced by AgNPs. Our studies clearly demonstrated a crucial role of naphthoquinones in AgNPs and extract interaction, as well as depicted the potential of AgNPs to restore the bactericidal activity of naphthoquinones towards P. aeruginosa. Our findings indicate the significant potential of nanoparticles to modulate the activity of selected secondary metabolites and revisit their antimicrobial potential towards human pathogenic bacteria.

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