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dc.contributor.authorMoni, M.A.en_AU
dc.contributor.authorQuinn, J.M.W.en_AU
dc.contributor.authorSinmaz, N.en_AU
dc.contributor.authorSummers, M.A.en_AU
dc.date.accessioned2021-06-02T04:55:22Z
dc.date.available2021-06-02T04:55:22Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/2123/25307
dc.description.abstractTo identify key gene expression pathways altered with infection of the novel coronavirus SARS-CoV-2, we performed the largest comparative genomic and transcriptomic analysis to date. We compared the novel pandemic coronavirus SARS-CoV-2 with SARS-CoV and MERS-CoV, as well as influenza A strains H1N1, H3N2 and H5N1. Phylogenetic analysis confirms that SARS-CoV-2 is closely related to SARS-CoV at the level of the viral genome. RNAseq analyses demonstrate that human lung epithelial cell responses to SARS-CoV-2 infection are distinct. Extensive Gene Expression Omnibus literature screening and drug predictive analyses show that SARS-CoV-2 infection response pathways are closely related to those of SARS-CoV and respiratory syncytial virus infections. We validated SARS-CoV-2 infection response genes as disease-associated using Kaplan-Meier survival estimates in lung disease patient data. We also analysed COVID-19 patient peripheral blood samples, which identified signalling pathway concordance between the primary lung cell and blood cell infection responses.en_AU
dc.language.isoenen_AU
dc.subjectCOVID-19en_AU
dc.subjectCoronavirusen_AU
dc.titleGene expression profiling of SARS-CoV-2 infections reveal distinct primary lung cell and systemic immune infection responses that identify pathways relevant in COVID-19 diseaseen_AU
dc.typeArticleen_AU
dc.identifier.doi10.1093/bib/bbaa376


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