%0 Journal Article
%T Initiator cell death event induced by SARS-CoV-2 in the human airway epithelium.
%A Liang K
%A Barnett KC
%A Hsu M
%A Chou WC
%A Bais SS
%A Riebe K
%A Xie Y
%A Nguyen TT
%A Oguin TH
%A Vannella KM
%A Hewitt SM
%A Chertow DS
%A Blasi M
%A Sempowski GD
%A Karlsson A
%A Koller BH
%A Lenschow DJ
%A Randell SH
%A Ting JP
%J Sci Immunol
%V 9
%N 97
%D 2024 Jul 12
%M 38996010
%F 30.63
%R 10.1126/sciimmunol.adn0178
%X Virus-induced cell death is a key contributor to COVID-19 pathology. Cell death induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is well studied in myeloid cells but less in its primary host cell type, angiotensin-converting enzyme 2 (ACE2)-expressing human airway epithelia (HAE). SARS-CoV-2 induces apoptosis, necroptosis, and pyroptosis in HAE organotypic cultures. Single-cell and limiting-dilution analysis revealed that necroptosis is the primary cell death event in infected cells, whereas uninfected bystanders undergo apoptosis, and pyroptosis occurs later during infection. Mechanistically, necroptosis is induced by viral Z-RNA binding to Z-DNA-binding protein 1 (ZBP1) in HAE and lung tissues from patients with COVID-19. The Delta (B.1.617.2) variant, which causes more severe disease than Omicron (B1.1.529) in humans, is associated with orders of magnitude-greater Z-RNA/ZBP1 interactions, necroptosis, and disease severity in animal models. Thus, Delta induces robust ZBP1-mediated necroptosis and more disease severity.