Broglie Jessica Jenkins, Alston Brittny, Yang Chang, Ma Lun, Adcock Audrey F, Chen Wei, Yang Liju
Biomanufacturing Research Institute and Technology Enterprise (BRITE), Department of Pharmaceutical Sciences, North Carolina Central University, Durham, North Carolina, United States of America.
Department of Physics, University of Texas at Arlington, Arlington, Texas, United States of America.
PLoS One. 2015 Oct 16;10(10):e0141050. doi: 10.1371/journal.pone.0141050. eCollection 2015.
Human norovirus is a leading cause of acute gastroenteritis worldwide in a plethora of residential and commercial settings, including restaurants, schools, and hospitals. Methods for easily detecting the virus and for treating and preventing infection are critical to stopping norovirus outbreaks, and inactivation via nanoparticles (NPs) is a more universal and attractive alternative to other physical and chemical approaches. Using norovirus GI.1 (Norwalk) virus-like particles (VLPs) as a model viral system, this study characterized the antiviral activity of Au/CuS core/shell nanoparticles (NPs) against GI.1 VLPs for the rapid inactivation of HuNoV. Inactivation of VLPs (GI.1) by Au/CuS NPs evaluated using an absorbance-based ELISA indicated that treatment with 0.083 μM NPs for 10 min inactivated ~50% VLPs in a 0.37 μg/ml VLP solution and 0.83 μM NPs for 10 min completely inactivated the VLPs. Increasing nanoparticle concentration and/or VLP-NP contact time significantly increased the virucidal efficacy of Au/CuS NPs. Changes to the VLP particle morphology, size, and capsid protein were characterized using dynamic light scattering, transmission electron microscopy, and Western blot analysis. The strategy reported here provides the first reported proof-of-concept Au/CuS NPs-based virucide for rapidly inactivating human norovirus.
人诺如病毒是全球范围内众多住宅和商业场所(包括餐馆、学校和医院)急性胃肠炎的主要病因。轻松检测该病毒以及治疗和预防感染的方法对于阻止诺如病毒爆发至关重要,而通过纳米颗粒(NPs)进行灭活是一种比其他物理和化学方法更具通用性和吸引力的替代方法。本研究以诺如病毒GI.1(诺沃克)病毒样颗粒(VLPs)作为模型病毒系统,表征了金/硫化铜核壳纳米颗粒(NPs)对GI.1 VLPs的抗病毒活性,以实现人诺如病毒的快速灭活。使用基于吸光度的酶联免疫吸附测定法评估金/硫化铜NPs对VLPs(GI.1)的灭活情况,结果表明,在0.37μg/ml的VLP溶液中,用0.083μM的NPs处理10分钟可使约50%的VLPs失活,而用0.83μM的NPs处理10分钟可使VLPs完全失活。增加纳米颗粒浓度和/或VLP-NP接触时间可显著提高金/硫化铜NPs的杀病毒效果。使用动态光散射、透射电子显微镜和蛋白质免疫印迹分析对VLP颗粒的形态、大小和衣壳蛋白的变化进行了表征。本文报道的策略首次提供了基于金/硫化铜NPs的杀病毒剂的概念验证,可快速灭活人类诺如病毒。