Antibacterial and antibiofilm activity of silver nanoparticles stabilized with C-phycocyanin against drug-resistant Pseudomonas aeruginosa and Staphylococcus aureus

被引:2
|
作者
Chegini, Zahra [1 ]
Shariati, Aref [2 ]
Alikhani, Mohammad Yousef [1 ]
Safaiee, Maliheh [3 ]
Rajaeih, Shahin [4 ]
Arabestani, Mohammadreza [1 ,5 ]
Azizi, Mehdi [6 ]
机构
[1] Hamadan Univ Med Sci, Sch Med, Dept Microbiol, Hamadan, Iran
[2] Arak Univ Med Sci, Infect Dis Res Ctr IDRC, Arak, Iran
[3] Bu Ali Sina Univ, Fac Chem & Petr Sci, Dept Organ Chem, Hamadan, Iran
[4] Iran Univ Med Sci, Senses Hlth Inst 5, ENT & Head & Neck Res Ctr & Dept, Tehran, Iran
[5] Hamadan Univ Med Sci, Infect Dis Res Ctr, Hamadan, Iran
[6] Hamadan Univ Med Sci, Dept Tissue Engn & Regenerat Med, Hamadan, Iran
关键词
silver nanoparticles; C-phycocyanin; biofilms; antibiotics-resistant; new treatment; IN-VITRO;
D O I
10.3389/fbioe.2024.1455385
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Biofilms are bacterial communities that can protect them against external factors, including antibiotics. In this study, silver nanoparticles (AgNPs) were formed by modifying AgNPs with C-phycocyanin (Ag-Pc) to inhibit the growth of carbapenem-resistant Pseudomonas aeruginosa (CR P. aeruginosa) and methicillin-resistant Staphylococcus aureus (MRSA) and destroy biofilm of these bacteria. Methods: The AgNPs were prepared with the green synthesis method, and Pc was used to stabilize the AgNPs. The Ag-Pc's antibacterial and antibiofilm effects were evaluated using the Microbroth dilution method and microtiter plate assay. The inhibitory effect of Ag-Pc on the expression of biofilm-related genes was evaluated by real-time PCR. Moreover, the MTT assay was used to assess the Ag-Pc toxicity. Results: The Ag-Pc minimum inhibitory concentration (MIC) was 7.4 mu g/mL for CR P. aeruginosa and MRSA. Pc did not show antibacterial effects against any of the strains. Ag-Pc suppressed biofilm formation and destroyed matured biofilm in both bacteria more efficiently than the AgNPs (P< 0.05). The expression of all genes was not significantly reduced in the presence of synthesized nanoparticles. Finally, the MTT assay results did not show toxicity against a murine fibroblast cell line (L929) at MIC concentration. Conclusion: The present study showed the promising potential of Pc for improving the antibacterial and antibiofilm function of AgNPs and inhibiting drug-resistant bacteria. Therefore, Ag-Pc nanoparticles can be considered a promising therapeutic approach for the managing of the bacterial biofilm.
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页数:13
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