<p><i>Staphylococcus aureus</i> (<i>S. aureus</i>) is a common cause of nosocomial infections, posing substantial public health challenges. The current study employed a synthesized zingerone-potassium-doped ZnO (Zin-K-ZnO) nanoparticles (NPs) against the growth and biofilm formation by <i>S. aureus</i>. A real-time PCR was used for assessment of the expression of antibiotic resistance and virulence factor (<i>mecA</i> and <i>spA</i>, respectively) in <i>S. aureus</i> under treatment with the NPs compared to control. 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide&#xa0;(MTT) assay was used to determine the cytotoxicity of the NPs based on the survival percentage of HCT-116 cells cultured with NPs of the concentration obtained for MIC. Structure analyses revealed that the NPs exhibited an approximately spherical morphology, with an average diameter of 37 nm. Antibacterial activity assessment demonstrated dose-dependent inhibition of <i>S. aureus</i> growth by the NPs. The minimum inhibitory concentration (MIC) of Zin-K-ZnO NPs (9.5 mM) was significantly lower than the value for zingerone (56 mM). Furthermore, Zin-K-ZnO NPs at the concentration of 64–1024 mg/mL prevented <i>S. aureus</i> biofilm formation by 19.9–81.0 ± 4.7%, which was significantly more effective compared to zingerone. Additionally, the NPs led to a substantial decrease in the expression of <i>spA</i> and <i>mecA</i> genes in <i>S. aureus</i>. MTT result revealed that NPs with the concentration of 9.5 mM had low cytotoxicity (92% cell viability) on HCT-116 cells. The results highlighted the strong antibacterial properties exhibited by both zingerone and Zin-K-ZnO NPs against <i>S. aureus</i> growth and biofilm formation.</p>

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Enhancing the Antimicrobial Effectiveness of Zinc Oxide Nanoparticles Against Staphylococcus aureus, Through Combination with Potassium and Zingerone

  • Raziyeh Frootan,
  • Farokh Rokhbakhsh-Zamin,
  • Abdollah Jafarzadeh,
  • Ebrahim Rezazadeh Zarandi,
  • Nadia Kazemipour

摘要

Staphylococcus aureus (S. aureus) is a common cause of nosocomial infections, posing substantial public health challenges. The current study employed a synthesized zingerone-potassium-doped ZnO (Zin-K-ZnO) nanoparticles (NPs) against the growth and biofilm formation by S. aureus. A real-time PCR was used for assessment of the expression of antibiotic resistance and virulence factor (mecA and spA, respectively) in S. aureus under treatment with the NPs compared to control. 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay was used to determine the cytotoxicity of the NPs based on the survival percentage of HCT-116 cells cultured with NPs of the concentration obtained for MIC. Structure analyses revealed that the NPs exhibited an approximately spherical morphology, with an average diameter of 37 nm. Antibacterial activity assessment demonstrated dose-dependent inhibition of S. aureus growth by the NPs. The minimum inhibitory concentration (MIC) of Zin-K-ZnO NPs (9.5 mM) was significantly lower than the value for zingerone (56 mM). Furthermore, Zin-K-ZnO NPs at the concentration of 64–1024 mg/mL prevented S. aureus biofilm formation by 19.9–81.0 ± 4.7%, which was significantly more effective compared to zingerone. Additionally, the NPs led to a substantial decrease in the expression of spA and mecA genes in S. aureus. MTT result revealed that NPs with the concentration of 9.5 mM had low cytotoxicity (92% cell viability) on HCT-116 cells. The results highlighted the strong antibacterial properties exhibited by both zingerone and Zin-K-ZnO NPs against S. aureus growth and biofilm formation.