生物
冠状病毒
呼吸道
病毒学
免疫学
病毒
呼吸系统
病理
疾病
2019年冠状病毒病(COVID-19)
医学
传染病(医学专业)
解剖
作者
Katrina B. Mar,Alexandra I. Wells,Marley C. Caballero Van Dyke,Alexandra H Lopez,Jennifer L. Eitson,Wenchun Fan,Natasha W. Hanners,Bret M. Evers,John M. Shelton,John W. Schoggins
出处
期刊:Nature microbiology
日期:2023-07-13
卷期号:8 (8): 1587-1599
被引量:9
标识
DOI:10.1038/s41564-023-01431-w
摘要
LY6E is an antiviral restriction factor that inhibits coronavirus spike-mediated fusion, but the cell types in vivo that require LY6E for protection from respiratory coronavirus infection are unknown. Here we used a panel of seven conditional Ly6e knockout mice to define which Ly6e-expressing cells confer control of airway infection by murine coronavirus and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Loss of Ly6e in Lyz2-expressing cells, radioresistant Vav1-expressing cells and non-haematopoietic cells increased susceptibility to murine coronavirus. Global conditional loss of Ly6e expression resulted in clinical disease and higher viral burden after SARS-CoV-2 infection, but little evidence of immunopathology. We show that Ly6e expression protected secretory club and ciliated cells from SARS-CoV-2 infection and prevented virus-induced loss of an epithelial cell transcriptomic signature in the lung. Our study demonstrates that lineage confined rather than broad expression of Ly6e sufficiently confers resistance to disease caused by murine and human coronaviruses. A panel of seven conditional Ly6e knockout mice are used to show that Ly6e expression protects the respiratory tract from severe acute respiratory syndrome coronavirus 2 and mouse hepatitis virus infection.
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