Journal
VIRUSES-BASEL
Volume 15, Issue 5, Pages -Publisher
MDPI
DOI: 10.3390/v15051166
Keywords
human airway organoids; epithelial polarity; SARS-CoV-2; Omicron variant
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Researchers have successfully established a three-dimensional organoid model of the respiratory epithelium, which accurately mimics the morphology and function of the human airway epithelium. This model allows for sustained replication of SARS-CoV-2 and accurately recapitulates the infectivity and replicative fitness of different viral variants. The model has significant importance in studying respiratory biology and diseases.
The respiratory epithelium, particularly the airway epithelium, is the primary infection site for respiratory pathogens. The apical surface of epithelial cells is constantly exposed to external stimuli including invading pathogens. Efforts have been made to establish organoid cultures to recapitulate the human respiratory tract. However, a robust and simple model with an easily accessible apical surface would benefit respiratory research. Here, we report the generation and characterization of apical-out airway organoids from the long-term expandable lung organoids that we previously established. The apical-out airway organoids morphologically and functionally recapitulated the human airway epithelium at a comparable level to the apical-in airway organoids. Moreover, apical-out airway organoids sustained productive and multicycle replication of SARS-CoV-2, and accurately recapitulated the higher infectivity and replicative fitness of the Omicron variants BA.5 and B.1.1.529 and an ancestral virus. In conclusion, we established a physiologically relevant and convenient apical-out airway organoid model for studying respiratory biology and diseases.
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