Single-cell longitudinal analysis of SARS-CoV-2 infection in human airway epithelium identifies target cells, alterations in gene expression, and cell state changes

Neal G. Ravindra(Yale University), Mia Madel Alfajaro(Yale University), Victor Gasque(Université Claude Bernard Lyon 1), Nicholas C. Huston(Yale University), Han Wan(Yale University), Klara Szigeti‐Buck(Yale University), Yuki Yasumoto(Yale University), Allison M. Greaney(Yale University), Victoria Habet(Yale University), Ryan D. Chow(Yale University), Jennifer Chen(Yale University), Jin Wei(Yale University), Renata B. Filler(Yale University), Bao Wang(Yale University), Guilin Wang, Laura E. Niklason(Yale University), Ruth R. Montgomery(Yale University), Stephanie C. Eisenbarth(Yale University), Sidi Chen(Yale University), Adam Williams(Jackson Laboratory), Akiko Iwasaki(Howard Hughes Medical Institute), Tamás L. Horváth(Yale University), Ellen F. Foxman(Yale University), Richard W. Pierce(Yale University), Anna Marie Pyle(Howard Hughes Medical Institute), David van Dijk(Yale University), Craig B. Wilen(Yale University)
PLoS Biology
March 17, 2021
Cited by 278Open Access
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Abstract

There are currently limited Food and Drug Administration (FDA)-approved drugs and vaccines for the treatment or prevention of Coronavirus Disease 2019 (COVID-19). Enhanced understanding of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection and pathogenesis is critical for the development of therapeutics. To provide insight into viral replication, cell tropism, and host-viral interactions of SARS-CoV-2, we performed single-cell (sc) RNA sequencing (RNA-seq) of experimentally infected human bronchial epithelial cells (HBECs) in air-liquid interface (ALI) cultures over a time course. This revealed novel polyadenylated viral transcripts and highlighted ciliated cells as a major target at the onset of infection, which we confirmed by electron and immunofluorescence microscopy. Over the course of infection, the cell tropism of SARS-CoV-2 expands to other epithelial cell types including basal and club cells. Infection induces cell-intrinsic expression of type I and type III interferons (IFNs) and interleukin (IL)-6 but not IL-1. This results in expression of interferon-stimulated genes (ISGs) in both infected and bystander cells. This provides a detailed characterization of genes, cell types, and cell state changes associated with SARS-CoV-2 infection in the human airway.


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