Zhu Ying, Warrick Jay W, Haubert Kathryn, Beebe David J, Yin John
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI 53706, USA.
Biomed Microdevices. 2009 Jun;11(3):565-70. doi: 10.1007/s10544-008-9263-7.
The plaque assay has long served as the "gold standard" to measure virus infectivity and test antiviral drugs, but the assay is labor-intensive, lacks sensitivity, uses excessive reagents, and is hard to automate. Recent modification of the assay to exploit flow-enhanced virus spread with quantitative imaging has increased its sensitivity. Here we performed flow-enhanced infection assays in microscale channels, employing passive fluid pumping to inoculate cell monolayers with virus and drive infection spread. Our test of an antiviral drug (5-fluorouracil) against vesicular stomatitis virus infections of BHK cell monolayers yielded a two-fold improvement in sensitivity, relative to the standard assay based on plaque counting. The reduction in scale, simplified fluid handling, image-based quantification, and higher assay sensitivity will enable infection measurements for high-throughput drug screening, sero-conversion testing, and patient-specific diagnosis of viral infections.
蚀斑测定长期以来一直是测量病毒感染性和测试抗病毒药物的“金标准”,但该测定劳动强度大、缺乏敏感性、试剂用量过多且难以自动化。最近对该测定进行了改进,利用流动增强病毒传播并结合定量成像,提高了其敏感性。在这里,我们在微尺度通道中进行了流动增强感染测定,采用被动流体泵送将病毒接种到细胞单层上并驱动感染传播。我们针对BHK细胞单层的水泡性口炎病毒感染测试了一种抗病毒药物(5-氟尿嘧啶),相对于基于蚀斑计数的标准测定,敏感性提高了两倍。规模的缩小、简化的流体处理、基于图像的定量以及更高的测定敏感性将使感染测量能够用于高通量药物筛选、血清转化测试以及病毒感染的患者特异性诊断。