Hagström Anna E V, Garvey Gavin, Paterson Andrew S, Dhamane Sagar, Adhikari Meena, Estes Mary K, Strych Ulrich, Kourentzi Katerina, Atmar Robert L, Willson Richard C
Department of Chemical and Biomolecular Engineering, University of Houston, Houston, Texas, United States of America.
Department of Biology and Biochemistry, University of Houston, Houston, Texas, United States of America.
PLoS One. 2015 May 15;10(5):e0126571. doi: 10.1371/journal.pone.0126571. eCollection 2015.
Noroviruses are recognized worldwide as the principal cause of acute, non-bacterial gastroenteritis, resulting in 19-21 million cases of disease every year in the United States. Noroviruses have a very low infectious dose, a short incubation period, high resistance to traditional disinfection techniques and multiple modes of transmission, making early, point-of-care detection essential for controlling the spread of the disease. The traditional diagnostic tools, electron microscopy, RT-PCR and ELISA require sophisticated and expensive instrumentation, and are considered too laborious and slow to be useful during severe outbreaks. In this paper we describe the development of a new, rapid and sensitive lateral-flow assay using labeled phage particles for the detection of the prototypical norovirus GI.1 (Norwalk), with a limit of detection of 107 virus-like particles per mL, one hundred-fold lower than a conventional gold nanoparticle lateral-flow assay using the same antibody pair.
诺如病毒在全球范围内被公认为急性非细菌性肠胃炎的主要病因,在美国每年导致1900万至2100万例疾病。诺如病毒具有极低的感染剂量、短潜伏期、对传统消毒技术的高抗性以及多种传播方式,这使得早期即时检测对于控制疾病传播至关重要。传统诊断工具,如电子显微镜、逆转录聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA),需要精密且昂贵的仪器设备,并且在严重疫情期间被认为过于繁琐和耗时,无法发挥作用。在本文中,我们描述了一种新型、快速且灵敏的侧向流动检测方法的开发,该方法使用标记的噬菌体颗粒来检测典型的诺如病毒GI.1(诺沃克病毒),检测限为每毫升107个病毒样颗粒,比使用相同抗体对的传统金纳米颗粒侧向流动检测方法低100倍。