Promising Antibiofilm Agents: Recent Breakthrough against Biofilm Producing Methicillin-Resistant Staphylococcus

Marwa I Abd El-Hamid1, El-Sayed Y El-Naenaeey1, Toka M Kandeel2

  • 1Department of Microbiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt.

Insights

Zinc oxide nanoparticles (ZnO NPs), proteinase K, and hamamelitannin (HAM) effectively inhibit multidrug-resistant Staphylococcus aureus (MRSA) biofilms. ZnO NPs also exhibit antimicrobial activity, offering a potent treatment option for MRSA infections.

Area of Science:

  • Microbiology
  • Nanotechnology
  • Infectious Diseases

Background:

  • Multidrug-resistant methicillin-resistant Staphylococcus aureus (MRSA) poses a significant global health threat due to its resistance to antibiotics.
  • The recalcitrant nature of MRSA biofilms contributes to treatment failure, necessitating the development of novel antibiofilm strategies.

Purpose of the Study:

  • To evaluate the antibiofilm efficacy of zinc oxide nanoparticles (ZnO NPs), proteinase K, and hamamelitannin (HAM) against MRSA biofilms.
  • To investigate the impact of these agents on the expression of key biofilm and quorum sensing genes in MRSA.
  • To assess the antimicrobial activity of the agents and their correlation with biofilm production and genotypic characteristics.

Main Methods:

  • Phenotypic and genotypic methods were employed to identify biofilm-producing MDR MRSA isolates.
  • Antimicrobial and antibiofilm activities of ZnO NPs, proteinase K, and HAM were assessed.
  • Transcriptional modulation of biofilm (icaA) and quorum sensing (agr) genes was analyzed.

Main Results:

  • ZnO NPs, proteinase K, and HAM demonstrated significant antibiofilm activity against MRSA biofilms.
  • These agents modulated the transcription of icaA and agr genes.
  • Only ZnO NPs exhibited potent antimicrobial activity against MRSA.
  • Biofilm production positively correlated with antimicrobial resistance and agr genotypes II and IV.

Conclusions:

  • ZnO NPs are recommended as standalone agents for their potent antimicrobial and antibiofilm properties against MDR MRSA.
  • Proteinase K and HAM can be used as adjunct therapies, co-administered with other antimicrobials, to manage MRSA biofilm infections.

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