Love Michelle E, Wiehler Shahina, Proud David
Department of Physiology and Pharmacology, and Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Methods Mol Biol. 2025;2903:65-75. doi: 10.1007/978-1-0716-4410-2_7.
The ability to titer virus is critical for quantifying the efficacy of interventions on viral replication as well as for monitoring the consistency and viability of viral stocks to ensure reproducible experiments. Infectious rhinovirus is quantified by determining the dilution of virus that infects and causes cytopathic effects in a permissive cell line. Here we outline a protocol for determining tissue culture infectious dose 50 (TCID) of rhinovirus-16 in WI-38 fibroblasts using an adapted microtiter plate system.
测定病毒滴度的能力对于量化干预措施对病毒复制的效果以及监测病毒储备液的一致性和活力以确保实验可重复性至关重要。传染性鼻病毒通过确定在允许性细胞系中感染并引起细胞病变效应的病毒稀释度来进行定量。在此,我们概述了一种使用改良的微量滴定板系统测定WI-38成纤维细胞中鼻病毒16的组织培养感染剂量50(TCID)的方案。