Author: Niu, Qian; Ma, Ling; Zhu, Shaobin; Li, Lan; Zheng, Qisheng; Hou, Jibo; Lian, Hong; Wu, Lina; Yan, Xiaomei
Title: Quantitative Assessment of the Physical Virus Titer and Purity by Ultrasensitive Flow Virometry Cord-id: 44xi6yf5 Document date: 2021_3_17
ID: 44xi6yf5
Snippet: Rapid quantification of viruses is vital for basic research on viral diseases as well as clinical application of virusâ€based products. Here, we report the development of a highâ€throughput singleâ€particle method to enumerate intact viral particles by ultrasensitive flow virometry, which detects single viruses as small as 27 nm in diameter. The nucleic acid dye SYTO 82 was used to stain the viral (or vector) genome, and a laboratoryâ€built nanoâ€flow cytometer (nFCM) was employed to simult
Document: Rapid quantification of viruses is vital for basic research on viral diseases as well as clinical application of virusâ€based products. Here, we report the development of a highâ€throughput singleâ€particle method to enumerate intact viral particles by ultrasensitive flow virometry, which detects single viruses as small as 27 nm in diameter. The nucleic acid dye SYTO 82 was used to stain the viral (or vector) genome, and a laboratoryâ€built nanoâ€flow cytometer (nFCM) was employed to simultaneously detect the sideâ€scatter and fluorescence signals of individual viral particles. Using the bacteriophage T7 as a model system, intact virions were completely discriminated from empty capsids and naked viral genomes. Successful measurement of the physical virus titer and purity was demonstrated for recombinant adenoviruses, which could be used for gene delivery, therapeutic products derived from phage cocktails, and infected cell supernatants for veterinary vaccine production.
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