Please use this identifier to cite or link to this item: https://doi.org/10.1128/MBIO.03436-21
Title: Human Nasal Epithelial Cells Sustain Persistent SARS-CoV-2 Infection In Vitro, despite Eliciting a Prolonged Antiviral Response
Authors: Gamage, Akshamal M 
Tan, Kai Sen 
Chan, Wharton OY
Lew, Zhe Zhang Ryan 
Liu, Jing 
Tan, Chee Wah 
Rajagopalan, Deepa
Lin, Quy Xiao Xuan
Tan, Le Min
Venkatesh, Prasanna Nori
Ong, Yew Kwang 
Thong, Mark
Lin, Raymond Tzer Pin
Prabhakar, Shyam
Wang, De Yun 
Wang, Lin-Fa 
Keywords: Science & Technology
Life Sciences & Biomedicine
Microbiology
COVID-19
nasal epithelial cells
SARS-CoV-2
single-cell sequencing
viral persistence
BAFF
Issue Date: 1-Jan-2022
Publisher: AMER SOC MICROBIOLOGY
Citation: Gamage, Akshamal M, Tan, Kai Sen, Chan, Wharton OY, Lew, Zhe Zhang Ryan, Liu, Jing, Tan, Chee Wah, Rajagopalan, Deepa, Lin, Quy Xiao Xuan, Tan, Le Min, Venkatesh, Prasanna Nori, Ong, Yew Kwang, Thong, Mark, Lin, Raymond Tzer Pin, Prabhakar, Shyam, Wang, De Yun, Wang, Lin-Fa (2022-01-01). Human Nasal Epithelial Cells Sustain Persistent SARS-CoV-2 Infection In Vitro, despite Eliciting a Prolonged Antiviral Response. MBIO 13 (1). ScholarBank@NUS Repository. https://doi.org/10.1128/MBIO.03436-21
Abstract: The dynamics of SARS-CoV-2 infection in COVID-19 patients are highly variable, with a subset of patients demonstrating prolonged virus shedding, which poses a significant challenge for disease management and transmission control. In this study, the long-term dynamics of SARS-CoV-2 infection were investigated using a human well-differentiated nasal epithelial cell (NEC) model of infection. NECs were observed to release SARS-CoV-2 virus onto the apical surface for up to 28 days postinfection (dpi), further corroborated by viral antigen staining. Single-cell transcriptome sequencing (sc-seq) was utilized to explore the host response from infected NECs after short-term (3-dpi) and long-term (28-dpi) infection. We identified a unique population of cells harboring high viral loads present at both 3 and 28 dpi, characterized by expression of cell stress-related genes DDIT3 and ATF3 and enriched for genes involved in tumor necrosis factor alpha (TNF-a) signaling and apoptosis. Remarkably, this sc-seq analysis revealed an antiviral gene signature within all NEC cell types even at 28 dpi. We demonstrate increased replication of basal cells, absence of widespread cell death within the epithelial monolayer, and the ability of SARS-CoV-2 to replicate despite a continuous interferon response as factors likely contributing to SARS-CoV-2 persistence. This study provides a model system for development of therapeutics aimed at improving viral clearance in immunocompromised patients and implies a crucial role for immune cells in mediating viral clearance from infected epithelia. IMPORTANCE Increasing medical attention has been drawn to the persistence of symptoms (long-COVID syndrome) or live virus shedding from subsets of COVID-19 patients weeks to months after the initial onset of symptoms. In vitro approaches to model viral or symptom persistence are needed to fully dissect the complex and likely varied mechanisms underlying these clinical observations. We show that in vitro differentiated human NECs are persistently infected with SARS-CoV-2 for up to 28 dpi. This viral replication occurred despite the presence of an antiviral gene signature across all NEC cell types even at 28 dpi. This indicates that epithelial cell intrinsic antiviral responses are insufficient for the clearance of SARS-CoV-2, implying an essential role for tissue-resident and infiltrating immune cells for eventual viral clearance from infected airway tissue in COVID-19 patients.
Source Title: MBIO
URI: https://scholarbank.nus.edu.sg/handle/10635/227546
ISSN: 21507511
DOI: 10.1128/MBIO.03436-21
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