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Relative infectivity of the SARS-CoV-2 Omicron variant in human alveolar cells

With the continuous emergence of highly transmissible SARS-CoV-2 variants, the comparison of their infectivity has become a critical issue for public health. However, a direct assessment of the viral characteristic has been challenging because of the lack of appropriate experimental models and effic...

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Detalles Bibliográficos
Autores principales: Kim, Taewoo, Min, Kyoung Il, Yang, Jeong-Sun, Kim, Jun Won, Cho, Junhyung, Kim, Yun Ho, Lee, Jeong Seok, Kim, Young Tae, Kim, Kyung-Chang, Kim, Jeong Yeon, Na, Kwon Joong, Lee, Joo-Yeon, Ju, Young Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659354/
https://www.ncbi.nlm.nih.gov/pubmed/36406862
http://dx.doi.org/10.1016/j.isci.2022.105571
Descripción
Sumario:With the continuous emergence of highly transmissible SARS-CoV-2 variants, the comparison of their infectivity has become a critical issue for public health. However, a direct assessment of the viral characteristic has been challenging because of the lack of appropriate experimental models and efficient methods. Here, we integrated human alveolar organoids and single-cell transcriptome sequencing to facilitate the evaluation. In a proof-of-concept study with four highly transmissible SARS-CoV-2 variants, including GR (B.1.1.119), Alpha (B.1.1.7), Delta (B.1.617.2), and Omicron (BA.1), a rapid evaluation of the relative infectivity was possible. Our system demonstrates that the Omicron variant is 5- to 7-fold more infectious to human alveolar cells than the other SARS-CoV-2 variants at the initial stage of infection. To our knowledge, for the first time, this study measures the relative infectivity of the Omicron variant under multiple virus co-infection and provides new experimental procedures that can be applied to monitor emerging viral variants.