Chung Soo, Breshears Lane E, Perea Sean, Morrison Christina M, Betancourt Walter Q, Reynolds Kelly A, Yoon Jeong-Yeol
Department of Biosystems Engineering, Department of Biomedical Engineering, Department of Chemical and Environmental Engineering, Department of Soil, Water and Environmental Science, and Mel and Enid Zuckerman College of Public Health, The University of Arizona, Tucson, Arizona 85721, United States.
ACS Omega. 2019 Jun 27;4(6):11180-11188. doi: 10.1021/acsomega.9b00772. eCollection 2019 Jun 30.
Human enteric viruses can be highly infectious and thus capable of causing disease upon ingestion of low doses ranging from 10 to 10 virions. Norovirus is a good example with a minimum infectious dose as low as a few tens of virions, that is, below femtogram scale. Norovirus detection from commonly implicated environmental matrices (water and food) involves complicated concentration of viruses and/or amplification of the norovirus genome, thus rendering detection approaches not feasible for field applications. In this work, norovirus detection was performed on a microfluidic paper analytic device without using any sample concentration or nucleic acid amplification steps by directly imaging and counting on-paper aggregation of antibody-conjugated, fluorescent submicron particles. An in-house developed smartphone-based fluorescence microscope and an image-processing algorithm isolated the particles aggregated by antibody-antigen binding, leading to an extremely low limit of norovirus detection, as low as 1 genome copy/μL in deionized water and 10 genome copies/μL in reclaimed wastewater.
人类肠道病毒具有高度传染性,因此摄入低至10到10个病毒粒子的剂量就能够引发疾病。诺如病毒就是一个很好的例子,其最低感染剂量低至几十 个病毒粒子,即低于飞克级别。从常见的相关环境基质(水和食物)中检测诺如病毒涉及复杂的病毒浓缩和/或诺如病毒基因组扩增,因此使得检测方法对于现场应用而言并不可行。在这项工作中,在微流控纸分析装置上进行诺如病毒检测时,无需任何样品浓缩或核酸扩增步骤,而是通过直接成像和计数抗体偶联的荧光亚微米颗粒在纸上的聚集情况来实现。一种内部开发的基于智能手机的荧光显微镜和图像处理算法分离出通过抗体-抗原结合而聚集的颗粒,从而实现了极低的诺如病毒检测限,在去离子水中低至1个基因组拷贝/μL,在再生废水中低至10个基因组拷贝/μL。