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        <identifier>oai:figshare.com:article/33285636</identifier>
        <datestamp>2026-09-21T09:24:03Z</datestamp>
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          <dc:title>Supporting data for "Comparing host response to SARS-CoV and SARS-CoV-2 in normal human bronchial epithelial cells and Syrian hamsters"</dc:title>
          <dc:creator>Chi Cheng Sou (18992261)</dc:creator>
          <dc:subject>Medical virology</dc:subject>
          <dc:subject>Syrian hamsters</dc:subject>
          <dc:subject>NHBE cells</dc:subject>
          <dc:subject>host response</dc:subject>
          <dc:subject>SARS-CoV</dc:subject>
          <dc:subject>SARS-CoV-2</dc:subject>
          <dc:subject>Omicron BA.1</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Differentiated normal human bronchial epithelial cells (NHBE) were infected with SARS-CoV (strain: HK39849) or SARS-CoV-2 (strain: hCoV-19/Hong Kong/VM0001061/ 2020) at an MOI of 0.5 or MOCK-infected with PBS, and were collected at 2h, 6h, 24h, 48h, and 72h post-infection (hpi) to determine viral load and host response by TCID50 and bulk RNA sequencing (RNAseq), respectively. Male Syrian hamsters were intranasally inoculated with 10&lt;sup&gt;5&lt;/sup&gt; TCID50 of SARS-CoV, SARS-CoV-2, or PBS. Nasal turbinates and lungs were collected on 1, 2, and 5 days post-inoculation (dpi) to determine viral load and host response. Gene-set enrichment analysis (GSEA) was used to identify pathways of significant biological functions.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-21T09:24:03Z</dc:date>
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          <dc:identifier>10.25442/hku.33285636.v1</dc:identifier>
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