Blue light irradiation triggers the antimicrobial potential of ZnO nanoparticles on drug-resistant Acinetobacter baumannii

J Photochem Photobiol B. 2018 Mar:180:235-242. doi: 10.1016/j.jphotobiol.2018.02.003. Epub 2018 Feb 6.

Abstract

Photodynamic inactivation (PDI) is a non-invasive and safe therapeutic method for microbial infections. Bacterial antibiotic resistance is caused by antibiotics abuse. Drug-resistant Acinetobacter spp. is a serious problem in hospitals around the world. These pathogens from nosocomial infections have high mortality rates in frailer people, and Acinetobacter spp. is commonly found in immunocompromised patients. Visible light is safer than ultraviolet light (UV) for PDI of nosocomial pathogens with mammalian cells. Zinc oxide nanoparticles (ZnO-NPs) were used in this study as an antimicrobial agent and a photosensitizer. ZnO is recognized as safe and has extensive usage in food additives, medical and cosmetic products. In this study, we used 0.125 mg/ml ZnO-NPs combined with 10.8 J/cm2 blue light (BL) on Acinetobacter baumannii (A. baumannii) that could significantly reduce microbial survival. However, individual exposure to ZnO-NPs does not affect the viability of A. baumannii. BL irradiation could trigger the antimicrobial ability of ZnO nanoparticles on A. baumannii. The mechanism of photocatalytic ZnO-NPs treatment for sterilization occurs through bacterial membrane disruptions. Otherwise, the photocatalytic ZnO-NPs treatment showed high microbial eradication in nosocomial pathogens, including colistin-resistant and imipenem-resistant A. baumannii and Klebsiella pneumoniae. Based on our results, the photocatalytic ZnO-NPs treatment could support hygiene control and clinical therapies without antibiotics to nosocomial bacterial infections.

Keywords: A. baumannii; Hospital-grade disinfectant; Light-emitting diode; Nosocomial pathogen; Photodynamic inactivation.

MeSH terms

  • Acinetobacter baumannii / drug effects*
  • Acinetobacter baumannii / radiation effects
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology*
  • Catalysis
  • Cell Wall / drug effects
  • Cell Wall / radiation effects
  • Colistin / pharmacology
  • Drug Resistance, Bacterial / drug effects*
  • Drug Resistance, Bacterial / radiation effects
  • Light*
  • Metal Nanoparticles / chemistry
  • Metal Nanoparticles / toxicity*
  • Microscopy, Electron, Transmission
  • Microscopy, Fluorescence
  • Photosensitizing Agents / chemistry
  • Photosensitizing Agents / pharmacology
  • Zinc Oxide / chemistry*

Substances

  • Anti-Infective Agents
  • Photosensitizing Agents
  • Zinc Oxide
  • Colistin