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Nasal ciliated cells are primary targets for SARS-CoV-2 replication in the early stage of COVID-19.


ABSTRACT: The upper respiratory tract is compromised in the early period of COVID-19, but SARS-CoV-2 tropism at the cellular level is not fully defined. Unlike recent single-cell RNA-Seq analyses indicating uniformly low mRNA expression of SARS-CoV-2 entry-related host molecules in all nasal epithelial cells, we show that the protein levels are relatively high and that their localizations are restricted to the apical side of multiciliated epithelial cells. In addition, we provide evidence in patients with COVID-19 that SARS-CoV-2 is massively detected and replicated within the multiciliated cells. We observed these findings during the early stage of COVID-19, when infected ciliated cells were rapidly replaced by differentiating precursor cells. Moreover, our analyses revealed that SARS-CoV-2 cellular tropism was restricted to the nasal ciliated versus oral squamous epithelium. These results imply that targeting ciliated cells of the nasal epithelium during the early stage of COVID-19 could be an ideal strategy to prevent SARS-CoV-2 propagation.

SUBMITTER: Ahn JH 

PROVIDER: S-EPMC8245175 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Nasal ciliated cells are primary targets for SARS-CoV-2 replication in the early stage of COVID-19.

Ahn Ji Hoon JH   Kim JungMo J   Hong Seon Pyo SP   Choi Sung Yong SY   Yang Myung Jin MJ   Ju Young Seok YS   Kim Young Tae YT   Kim Ho Min HM   Rahman M D Tazikur MDT   Chung Man Ki MK   Hong Sang Duk SD   Bae Hosung H   Lee Chang-Seop CS   Koh Gou Young GY  

The Journal of clinical investigation 20210701 13


The upper respiratory tract is compromised in the early period of COVID-19, but SARS-CoV-2 tropism at the cellular level is not fully defined. Unlike recent single-cell RNA-Seq analyses indicating uniformly low mRNA expression of SARS-CoV-2 entry-related host molecules in all nasal epithelial cells, we show that the protein levels are relatively high and that their localizations are restricted to the apical side of multiciliated epithelial cells. In addition, we provide evidence in patients with  ...[more]

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