On the Calculation of TCID50 for Quantitation of Virus Infectivity |
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Authors: | Lei Chengfeng Yang Jian Hu Jia Sun Xiulian |
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Affiliation: | 1.Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan 430071, China2.University of Chinese Academy of Sciences, Beijing 100049, China |
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Abstract: | The most important property of a virus is its infectivity. To measure infectivity, one can assay viral replication in cells to obtain a titer for a given virus stock. A titer is defined as a given number of infectious viral units per unit volume, and an infectious unit is the smallest amount of virus that produces recognizable effects [e.g., cytopathic effect (CPE), dot blot immunoreactivity]. The median tissue culture infectious dose (TCID50) is defined as the dilution of a virus required to infect 50% of a given cell culture. Several methods have been developed to calculate the TCID50 including the Spearman–K?rber method (Spearman 1908; K?rber 1931), the Reed–Muench method (Reed and Muench 1938), the improved K?rber method (Sun 1963), the Weil method (Meynell GG and Meynell E 1970), and probit/logit regression models (Finney 1971). In this letter, we analyze datasets using three popular methods for calculating the TCID50 in Excel based calculator (Supplementary file 1). We also compared these results with those of probit/logit regression models and discuss the differences among these methods. |
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