病毒定量
单纯疱疹病毒
污渍
病毒学
染色
水泡性口炎病毒
病毒
斑块形成单元
溶解
溶瘤病毒
溶解循环
生物
分子生物学
化学
病理
医学
作者
Tairan Liu,Yuzhu Li,Hatice Ceylan Koydemir,Yijie Zhang,Ethan Yang,Merve Eryılmaz,Hongda Wang,Jingxi Li,Bijie Bai,Guangdong Ma,Aydogan Ozcan
标识
DOI:10.1038/s41551-023-01057-7
摘要
Abstract A plaque assay—the gold-standard method for measuring the concentration of replication-competent lytic virions—requires staining and usually more than 48 h of runtime. Here we show that lens-free holographic imaging and deep learning can be combined to expedite and automate the assay. The compact imaging device captures phase information label-free at a rate of approximately 0.32 gigapixels per hour per well, covers an area of about 30 × 30 mm 2 and a 10-fold larger dynamic range of virus concentration than standard assays, and quantifies the infected area and the number of plaque-forming units. For the vesicular stomatitis virus, the automated plaque assay detected the first cell-lysing events caused by viral replication as early as 5 h after incubation, and in less than 20 h it detected plaque-forming units at rates higher than 90% at 100% specificity. Furthermore, it reduced the incubation time of the herpes simplex virus type 1 by about 48 h and that of the encephalomyocarditis virus by about 20 h. The stain-free assay should be amenable for use in virology research, vaccine development and clinical diagnosis.
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