Evaluation of the Antimicrobial Activity of ZnO Nanoparticles against Enterotoxigenic Staphylococcus aureus

Reham M El-Masry1, Dalia Talat2, Shahira A Hassoubah3

  • 1Directorate of Veterinary Medicine, El-Gharbia 31515, Egypt.

Life (Basel, Switzerland)
|October 27, 2022
PubMed

Insights

Zinc oxide nanoparticles (ZnO NPs) show potent antibacterial effects against Staphylococcus aureus, reducing bacterial growth and enterotoxin A production. ZnO NPs also disrupt bacterial cell morphology and affect specific genes, offering a promising strategy against antibiotic resistance.

Area of Science:

  • Nanotechnology
  • Microbiology
  • Materials Science

Background:

  • Staphylococcus aureus (S. aureus) is a major cause of bacterial infections, with antibiotic resistance posing a significant global health challenge.
  • Metal nanoparticles and their oxides are being explored as novel antimicrobial agents to combat antibiotic-resistant bacteria.

Purpose of the Study:

  • To investigate the antibacterial efficacy of zinc oxide nanoparticles (ZnO NPs) against enterotoxigenic S. aureus.
  • To evaluate the impact of ZnO NPs on S. aureus growth, enterotoxin production, gene expression, and cell morphology.

Main Methods:

  • In vitro antibacterial activity assessed using agar diffusion tests and minimum inhibitory concentration (MIC) determination.
  • Bacterial growth reduction quantified, and enterotoxin A levels measured via ELISA.
  • Gene expression analysis using PCR (targeting sea and nuc genes) and morphological changes observed using scanning electron microscopy (SEM).

Main Results:

  • ZnO NPs demonstrated significant zones of inhibition and reduced bacterial counts, with a 98.99% growth reduction observed with 20 nm ZnO NPs at 10 mM.
  • MIC values varied based on ZnO NP size and bacterial concentration, ranging from 2.5 to 5 mM.
  • ELISA and PCR results confirmed a significant decrease in enterotoxin A and disruption of the sea gene, respectively, with no effect on the nuc gene. SEM revealed morphological damage to bacterial cells.

Conclusions:

  • ZnO NPs exhibit potent antibacterial properties against S. aureus, effectively inhibiting growth, reducing enterotoxin A, and damaging bacterial cells.
  • The observed effects on the sea gene suggest a mechanism involving gene expression modulation.
  • ZnO NPs represent a promising alternative strategy to combat antibiotic-resistant S. aureus infections.