Silver Nanoparticle-Aminogylcosides Conjugation for Enhanced Control of Pathogenic E. Coli O157:H7

被引:2
作者
Lee, Eon-Bee [1 ]
Lee, Kyubae [2 ]
机构
[1] Kyungpook Natl Univ, Coll Vet Med, Lab Vet Pharmacokinet & Pharmacodynam, Daegu 41566, South Korea
[2] Konyang Univ, Dept Biomed Mat, Daejeon 35365, South Korea
基金
新加坡国家研究基金会;
关键词
Silver nanoparticles; Aminoglycosides; E; coli; Antibacterial resistance; AMINOGLYCOSIDE RESISTANCE; MECHANISM; ENZYME; INDEX; ARMA;
D O I
10.1007/s10904-024-03015-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This study ventures into unexplored realms by investigating the combined efficacy of aminoglycosides (amikacin (AMI), gentamicin (GEN), kanamycin (KAN), streptomycin (STR), and tobramycin (TOB)) and silver nanoparticles (AgNPs) against pathogenic E. coli, offering a novel approach to combating antibiotic resistance. A noticeable transformation in color from a soft yellow to a rich brown marked the transition of silver ions to AgNPs, a process visually captured over 42 h. Morphological investigations showcased untreated E. coli cells retaining their natural rod shape, contrasted by AgNP treated cells that displayed considerable structural damage, signifying compromised cellular integrity. Antibacterial experiments, involving MIC and MBC tests, unveiled an increased effectiveness of antibiotics when paired with AgNPs, demonstrating a remarkable synergistic relationship. Time-kill assays provided a bacterial reductions, highlighting the boosted antibacterial action resulting from the combined application of AgNPs and antibiotics. The combination of TOB with AgNPs displayed the most substantial biofilm reduction, reaching at 19.87%. Fascinatingly, the armA gene was observed in bacterial cultures exposed to a TOB (2MIC), but its non-detection in cultures treated with a mix of 2MIC TOB and AgNP stood out as particularly noteworthy. This research unveiled a crucial finding where the antibacterial effectiveness of aminoglycosides consistently improved when combined with AgNPs. The findings suggested a promising direction for further research into the synergistic effects of antibiotics and nanoparticle adjuncts. Understanding the underlying mechanisms of this interaction could provide valuable insights into combating bacterial resistance, particularly in strains that are resistant to conventional antibiotic treatments.
引用
收藏
页码:2800 / 2811
页数:12
相关论文
共 56 条
[1]   Effect of Titanium Dioxide Nanoparticles on the Expression of Efflux Pump and Quorum-Sensing Genes in MDR Pseudomonas aeruginosa Isolates [J].
Ahmed, Fatma Y. ;
Aly, Usama Farghaly ;
Abd El-Baky, Rehab Mahmoud ;
Waly, Nancy G. F. M. .
ANTIBIOTICS-BASEL, 2021, 10 (06)
[2]  
[Anonymous], 2017, Performance Standards for Antimicrobial Susceptibility Testing, V27th
[3]   Silver Nanoparticles and Their Antibacterial Applications [J].
Bruna, Tamara ;
Maldonado-Bravo, Francisca ;
Jara, Paul ;
Caro, Nelson .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (13)
[4]  
Cavallo G, 1981, G Batteriol Virol Immunol, V74, P335
[5]   The role of drinking water in the transmission of antimicrobial-resistant E. coli [J].
Coleman, B. L. ;
Salvadori, M. I. ;
McGeer, A. J. ;
Sibley, K. A. ;
Neumann, N. F. ;
Bondy, S. J. ;
Gutmanis, I. A. ;
McEwen, S. A. ;
Lavoie, M. ;
Strong, D. ;
Johnson, I. ;
Jamieson, F. B. ;
Louie, M. .
EPIDEMIOLOGY AND INFECTION, 2012, 140 (04) :633-642
[6]   Origins and Evolution of Antibiotic Resistance [J].
Davies, Julian ;
Davies, Dorothy .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2010, 74 (03) :417-+
[7]   Silver Release from Silver Nanoparticles in Natural Waters [J].
Dobias, J. ;
Bernier-Latmani, R. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2013, 47 (09) :4140-4146
[8]   Aminoglycoside Resistance The Emergence of Acquired 16S Ribosomal RNA Methyltransferases [J].
Doi, Yohei ;
Wachino, Jun-ichi ;
Arakawa, Yoshichika .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2016, 30 (02) :523-+
[9]   The aminoglycosides [J].
Edson, RS ;
Terrell, CL .
MAYO CLINIC PROCEEDINGS, 1999, 74 (05) :519-528
[10]  
Food H. Drug Administration, 2016, JUD US MED IMP ANT D