Does Conjugation of Silver Nanoparticles with Thiosemicarbazide Increase Their Antibacterial Properties?
Tayebeh HonarmandArdalan Panahi SharifAli SalehzadehAmir JalaliIraj NikokarPublished in: Microbial drug resistance (Larchmont, N.Y.) (2022)
The opportunistic pathogen, Pseudomonas aeruginosa , uses different mechanisms as well as biofilm production to acquire antibiotic resistance. The polysaccharide synthesis locus ( psl ) genes play an important role in P. aeruginosa biofilm formation. Therefore, targeting the expression of psl genes can be a suitable strategy to prevent the formation of biofilms by antibiotic-resistant strains. Today, advances in nanotechnology provide a novel potential strategy to combat antibiotic-resistant bacteria. In this study, the silver nanoparticles (Ag NPs) synthesized using a chemical co-precipitation method and, after conjugation with thiosemicarbazide, their effect on the biofilm-forming ability are studied in P. aeruginosa isolates. Chemical properties of synthesized nanoparticles were determined by scanning and transmission electron microscopy, Fourier transform infrared spectroscopy, diffuse reflectance spectroscopy, ultraviolet-visible spectroscopy, X-ray diffraction, and energy dispersive X-ray spectroscopy. The results confirmed the spherical/cubic morphology, solution stability, and good dispersion of Ag@Glu-TSC NPs with an average size of 40-60 nm. In addition, minimum inhibitory concentration values of functionalized Ag NPs were at least twofold lower than the Ag NPs (alone). The quantitative PCR data analysis showed a decrease in the expression of the pslA gene in the presence of Ag@Glu-TSC NPs, up to 60%, which was associated with a reduction of biofilm formation compared to control. In conclusion, the Ag@Glu-TSC NPs can be considered a new inhibitor of biofilm production in antibiotic-resistant bacteria.
Keyphrases
- biofilm formation
- pseudomonas aeruginosa
- silver nanoparticles
- candida albicans
- electron microscopy
- quantum dots
- high resolution
- staphylococcus aureus
- oxide nanoparticles
- escherichia coli
- cystic fibrosis
- highly efficient
- data analysis
- visible light
- poor prognosis
- genome wide
- acinetobacter baumannii
- single molecule
- genome wide identification
- drug delivery
- gas chromatography
- copy number
- photodynamic therapy
- binding protein
- genome wide analysis
- human health
- risk assessment
- drug resistant
- magnetic resonance
- computed tomography