Cao Ling, Tan Lili, Li Liping
Department of Clinical Laboratory, The Third Affiliated Hospital of Nanchang University (The First Hospital of Nanchang) Nanchang 330008, Jiangxi, P. R. China.
Am J Transl Res. 2024 May 15;16(5):2011-2023. doi: 10.62347/DIEO8870. eCollection 2024.
The increasing issue of bacterial resistance, coupled with inadequate progress in developing new antibiotics, necessitates exploring alternative treatments. Antibacterial biomaterials, such as silver and copper, possess advantageous properties such as heat resistance, durability, continuity, and safety. Particularly, they can effectively eliminate pathogenic bacteria while preserving cellular integrity, emphasizing the necessity of identifying optimal metal ion concentrations for practical application. () can serve as a noteworthy model in this context. This study employed a infection model to assess the efficacy of antibacterial metal ions.
Hematoxylin-eosin (HE) staining and inductively coupled plasma mass spectrometry (ICP-MS) assay were utilized to determine the toxic levels of metal ions in mice. Additionally, RNA sequencing (RNA-seq) and assessment of reactive oxygen species (ROS) production in the model were conducted to elucidate the mechanisms underlying metal ion toxicity.
Silver ion concentrations ranging from 10 to 10 M and copper ion concentrations ranging from 10 to 10 M exhibited antimicrobial properties without eliciting cytotoxic effects. Analysis of the transcriptome data derived from mRNA isolated from indicated that CRKP infection activated the FoxO signaling pathway, potentially leading to ROS accumulation and demise.
In conclusion, serves as a comprehensive infection model for assessing antibacterial metal ions.
细菌耐药性问题日益严重,加上新型抗生素研发进展不足,因此有必要探索替代治疗方法。抗菌生物材料,如银和铜,具有耐热、耐用、连续和安全等有利特性。特别是,它们可以有效消除病原菌,同时保持细胞完整性,这强调了确定实际应用中最佳金属离子浓度的必要性。()在这种情况下可以作为一个值得注意的模型。本研究采用感染模型来评估抗菌金属离子的疗效。
采用苏木精-伊红(HE)染色和电感耦合等离子体质谱(ICP-MS)测定法来确定小鼠体内金属离子的毒性水平。此外,进行了RNA测序(RNA-seq)和模型中活性氧(ROS)产生的评估,以阐明金属离子毒性的潜在机制。
浓度范围为10至10 M的银离子和浓度范围为10至10 M的铜离子具有抗菌特性,且未引起细胞毒性作用。对从分离出的mRNA获得的转录组数据进行分析表明,CRKP感染激活了FoxO信号通路,可能导致ROS积累和细胞死亡。
总之,可以作为评估抗菌金属离子的综合感染模型。