Yang Tsung-Ying, Kao Hao-Yun, Lu Po-Liang, Chen Pei-Yu, Wang Shu-Chi, Wang Liang-Chun, Hsieh Ya-Ju, Tseng Sung-Pin
Department of Medical Laboratory Science and Biotechnology, College of Health Sciences, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Department of Healthcare Administration and Medical Informatics, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Pharmaceuticals (Basel). 2021 Aug 12;14(8):795. doi: 10.3390/ph14080795.
Colistin- and carbapenem-resistant cases are increasing at alarming rates worldwide. Drug repurposing is receiving greater attention as an alternative approach in light of economic and technical barriers in antibiotics research. The immunomodulation agent ammonium trichloro(dioxoethylene-,'-)tellurate (AS101) was repurposed as an antimicrobial agent against colistin- and carbapenem-resistant (CRKP). 134 CRKP isolates were collected between 2012 and 2015 in Taiwan. The in vitro antibacterial activities of AS101 was observed through broth microdilution, time-kill assay, and electron microscopy. Pharmaceutical manipulation and RNA microarray were applied to investigate these antimicrobial mechanisms. , a nematode animal model, and the Institute for Cancer Research (ICR) mouse model was employed for the evaluation of in vivo efficacy. The in vitro antibacterial results were found for AS101 against colistin- and CRKP isolates, with minimum inhibitory concentration (MIC) values ranging from <0.5 to 32 μg/mL. ROS-mediated antibacterial activity eliminated 99.9% of bacteria within 2-4 h. AS101 also extended the median survival time in a animal model infected with a colistin-resistant CRKP isolate and rescued lethally infected animals in a separate mouse model of mono-bacterial sepsis by eliminating bacterial organ loads. These findings support the use of AS101 as an antimicrobial agent for addressing the colistin and carbapenem resistance crisis.
耐黏菌素和碳青霉烯类的病例在全球正以惊人的速度增加。鉴于抗生素研究中的经济和技术障碍,药物重新利用作为一种替代方法正受到更多关注。免疫调节剂三氯(二氧乙烯 - ,'-)碲酸铵(AS101)被重新用作抗耐黏菌素和耐碳青霉烯类(CRKP)的抗菌剂。2012年至2015年期间在台湾收集了134株CRKP分离株。通过肉汤微量稀释法、时间杀菌试验和电子显微镜观察了AS101的体外抗菌活性。应用药物操作和RNA微阵列来研究这些抗菌机制。使用线虫动物模型和癌症研究所(ICR)小鼠模型评估体内疗效。发现AS101对耐黏菌素和CRKP分离株有体外抗菌结果,最低抑菌浓度(MIC)值范围为<0.5至32μg/mL。ROS介导的抗菌活性在2 - 4小时内消除了99.9%的细菌。AS101还延长了感染耐黏菌素的CRKP分离株的线虫动物模型的中位生存时间,并通过消除细菌器官负荷在单独的单菌败血症小鼠模型中挽救了致命感染的动物。这些发现支持将AS101用作解决耐黏菌素和碳青霉烯类耐药危机的抗菌剂。