<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shaath H</submitter><funding>Qatar Biomedical Research institute</funding><pagination>E260</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7564677</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(9)</volume><pubmed_abstract>The continuous and rapid emergence of new viral strains calls for a better understanding of the fundamental changes occurring within the host cell upon viral infection. In this study, we analyzed RNA-seq transcriptome data from Calu-3 human lung epithelial cells infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) compared to five other viruses namely, severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East Respiratory Syndrome (SARS-MERS), influenzavirus A (FLUA), influenzavirus B (FLUB), and rhinovirus (RHINO) compared to mock-infected cells and characterized their coding and noncoding RNA transcriptional portraits. The induction of interferon, inflammatory, and immune response was a hallmark of SARS-CoV-2 infection. Comprehensive bioinformatics reveal</pubmed_abstract><journal>Biology</journal><pubmed_title>Computational and Transcriptome Analyses Revealed Preferential Induction of Chemotaxis and Lipid Synthesis by SARS-CoV-2.</pubmed_title><pmcid>PMC7564677</pmcid><funding_grant_id>QB13</funding_grant_id><pubmed_authors>Alajez NM</pubmed_authors><pubmed_authors>Shaath H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Computational and Transcriptome Analyses Revealed Preferential Induction of Chemotaxis and Lipid Synthesis by SARS-CoV-2.</name><description>The continuous and rapid emergence of new viral strains calls for a better understanding of the fundamental changes occurring within the host cell upon viral infection. In this study, we analyzed RNA-seq transcriptome data from Calu-3 human lung epithelial cells infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) compared to five other viruses namely, severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East Respiratory Syndrome (SARS-MERS), influenzavirus A (FLUA), influenzavirus B (FLUB), and rhinovirus (RHINO) compared to mock-infected cells and characterized their coding and noncoding RNA transcriptional portraits. The induction of interferon, inflammatory, and immune response was a hallmark of SARS-CoV-2 infection. Comprehensive bioinformatics reveal</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2026-04-08T00:39:04.489Z</modification><creation>2020-11-01T08:24:03Z</creation></dates><accession>S-EPMC7564677</accession><cross_references><pubmed>32882823</pubmed><doi>10.3390/biology9090260</doi></cross_references></HashMap>