<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Otter CJ</submitter><pubmed_abstract>The nasal epithelium is the initial entry portal and primary barrier to infection by all human coronaviruses (HCoVs). We utilize primary nasal epithelial cells grown at air-liquid interface, which recapitulate the heterogeneous cellular population as well as mucociliary clearance functions of the &lt;i>in vivo&lt;/i> nasal epithelium, to compare lethal (SARS-CoV-2 and MERS-CoV) and seasonal (HCoV-NL63 and HCoV-229E) HCoVs. All four HCoVs replicate productively in nasal cultures but diverge significantly in terms of cytotoxicity induced following infection, as the seasonal HCoVs as well as SARS-CoV-2 cause cellular cytotoxicity as well as epithelial barrier disruption, while MERS-CoV does not. Treatment of nasal cultures with type 2 cytokine IL-13 to mimic asthmatic airways differentially impacts</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2022.10.17.512617</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9603826</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Infection of primary nasal epithelial cells differentiates among lethal and seasonal human coronaviruses.</pubmed_title><pmcid>PMC9603826</pmcid><pubmed_authors>Cohen NA</pubmed_authors><pubmed_authors>Fausto A</pubmed_authors><pubmed_authors>Weiss SR</pubmed_authors><pubmed_authors>Tan LH</pubmed_authors><pubmed_authors>Otter CJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Infection of primary nasal epithelial cells differentiates among lethal and seasonal human coronaviruses.</name><description>The nasal epithelium is the initial entry portal and primary barrier to infection by all human coronaviruses (HCoVs). We utilize primary nasal epithelial cells grown at air-liquid interface, which recapitulate the heterogeneous cellular population as well as mucociliary clearance functions of the &lt;i>in vivo&lt;/i> nasal epithelium, to compare lethal (SARS-CoV-2 and MERS-CoV) and seasonal (HCoV-NL63 and HCoV-229E) HCoVs. All four HCoVs replicate productively in nasal cultures but diverge significantly in terms of cytotoxicity induced following infection, as the seasonal HCoVs as well as SARS-CoV-2 cause cellular cytotoxicity as well as epithelial barrier disruption, while MERS-CoV does not. Treatment of nasal cultures with type 2 cytokine IL-13 to mimic asthmatic airways differentially impacts</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-05T11:28:30.974Z</modification><creation>2025-04-05T11:28:30.974Z</creation></dates><accession>S-EPMC9603826</accession><cross_references><pubmed>36299422</pubmed><doi>10.1101/2022.10.17.512617</doi></cross_references></HashMap>