Antisense Oligonucleotide-Capped Gold Nanoparticles as a Potential Strategy for Tackling Antimicrobial Resistance

被引:0
作者
Rodolfo Garza-Cardenas, Cesar [1 ,2 ]
Leon-Buitimea, Angel [1 ,2 ]
Siller-Ceniceros, A. A. [1 ,2 ]
Ruben Morones-Ramirez, Jose [1 ,2 ]
机构
[1] Univ Autonoma Nuevo Leon, Fac Ciencias Quim, San Nicolas De Los Garza 66455, Mexico
[2] Univ Autonoma Nuevo Leon, Fac Ciencias Quim, Ctr Invest Biotecnol & Nanotecnol, Parque Invest & Innovac Tecnol, Apodaca 66628, Mexico
关键词
antisense oligonucleotide; gene silencing; gold nanoparticles; antimicrobial resistance; combination therapy; beta-lactam antibiotics; nanomedicine; ESCHERICHIA-COLI; BETA-LACTAMASES; DNA; REVERSION; DELIVERY; RNA;
D O I
10.3390/microbiolres16030070
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Multidrug-resistant (MDR) bacterial pathogens pose a serious threat to global health, underscoring the urgent need for innovative therapeutic strategies. In this work, we designed and characterized thiol-modified antisense oligonucleotide-capped gold nanoparticles (ASO-AuNPs) to resensitize antibiotic-resistant bacteria. Transmission electron microscopy and UV-Vis spectroscopy confirmed the morphology, size, and optical properties of AuNPs and ASO-AuNPs. Minimum inhibitory concentrations (MIC) of ampicillin were determined for non-resistant Escherichia coli DH5 alpha (16 ppm) and an ampicillin-resistant E. coli DH5 alpha strain (PSK, 32,768 ppm). When co-administered with ampicillin, ASO-AuNPs (0.1 and 0.2 nM) significantly reduced bacterial growth compared to the antibiotic-alone control (p < 0.05), demonstrating the capacity of ASO-AuNPs to restore antibiotic efficacy. These findings provide a proof of concept that antisense oligonucleotide-functionalized nanomaterials can be harnessed to overcome beta-lactam resistance, setting the stage for further optimization and translation into clinical applications.
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页数:20
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