Exploring the efficacy of tryptone-stabilized silver nanoparticles against respiratory tract infection-causing

Pooja Pandey1, Sristi Pradhan1, Kimaya Meher1

  • 1School of Biological Sciences, UM-DAE Centre for Excellence in Basic Sciences, University of Mumbai, Vidyanagari, Kalina Campus, Mumbai 400098, India.

Insights

Tryptone stabilized silver nanoparticles (Ts-AgNPs) show potent antimicrobial activity against Klebsiella pneumoniae and Pseudomonas aeruginosa. These nanoparticles effectively inhibit and eradicate bacterial biofilms, offering a novel therapeutic approach for respiratory tract infections.

Area of Science:

  • Nanotechnology
  • Microbiology
  • Infectious Diseases

Background:

  • Antibiotic resistance is a growing global health crisis, driven by the overuse of antibiotics for respiratory tract infections (RTIs).
  • Multidrug-resistant bacteria pose a significant threat, necessitating the development of novel therapeutic strategies.
  • Bacterial biofilms contribute to persistent infections and antibiotic resistance.

Purpose of the Study:

  • To investigate the antimicrobial potential of tryptone stabilized silver nanoparticles (Ts-AgNPs) against Klebsiella pneumoniae and Pseudomonas aeruginosa.
  • To evaluate the efficacy of Ts-AgNPs in inhibiting and eradicating bacterial biofilms.
  • To explore the mechanism of action of Ts-AgNPs, including their effect on virulence factors.

Main Methods:

  • Determined the minimum inhibitory concentration (MIC50) of Ts-AgNPs against planktonic bacteria.
  • Assessed the antimicrobial effect using time-kill curves and colony-forming unit counts.
  • Evaluated biofilm inhibition and eradication capabilities, and analyzed extracellular DNA (eDNA) and extracellular polymeric substance (EPS) quantity.
  • Investigated the impact of Ts-AgNPs on quorum sensing (QS)-induced virulence factors.

Main Results:

  • Ts-AgNPs exhibited low MIC50 values (1.7 μg ml⁻¹ for K. pneumoniae, 2.7 μg ml⁻¹ for P. aeruginosa).
  • Demonstrated significant reduction in bacterial growth and colony-forming units, indicating potent antimicrobial activity.
  • Achieved high biofilm inhibition (up to 93%) and eradication (up to 97%) rates.
  • Showed a decrease in eDNA and EPS, disrupting biofilm structure, and attenuated QS-induced virulence factors.

Conclusions:

  • Ts-AgNPs possess significant antimicrobial and anti-biofilm properties against K. pneumoniae and P. aeruginosa.
  • The nanoparticles disrupt biofilm matrix and reduce bacterial virulence, suggesting a novel mechanism of action.
  • Ts-AgNPs hold promise as a new class of antibiotics for treating RTIs caused by bacterial biofilms.