猪流行性腹泻病毒
冠状病毒
病毒学
纳米团簇
病毒复制
病毒
核糖核酸
生物
病毒结构蛋白
维罗细胞
沙粒病毒
萌芽
病毒进入
病毒包膜
2019年冠状病毒病(COVID-19)
细胞生物学
基因
材料科学
免疫学
免疫系统
医学
生物化学
纳米技术
CD8型
传染病(医学专业)
病理
疾病
淋巴细胞性脉络膜脑膜炎
作者
Ting Du,Jiangong Liang,Nan Dong,Jian Lü,Yiying Fu,Liurong Fang,Shaobo Xiao,Heyou Han
标识
DOI:10.1021/acsami.7b13811
摘要
Development of novel antiviral reagents is of great importance for the control of virus spread. Here, Ag2S nanoclusters (NCs) were proved for the first time to possess highly efficient antiviral activity by using porcine epidemic diarrhea virus (PEDV) as a model of coronavirus. Analyses of virus titers showed that Ag2S NCs significantly suppressed the infection of PEDV by about 3 orders of magnitude at the noncytotoxic concentration at 12 h postinfection, which was further confirmed by the expression of viral proteins. Mechanism investigations indicated that Ag2S NCs treatment inhibits the synthesis of viral negative-strand RNA and viral budding. Ag2S NCs treatment was also found to positively regulate the generation of IFN-stimulating genes (ISGs) and the expression of proinflammation cytokines, which might prevent PEDV infection. This study suggest the novel underlying of Ag2S NCs as a promising therapeutic drug for coronavirus.
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