Gene expression profiling of SARS-CoV-2 infections reveal distinct primary lung cell and systemic immune infection responses that identify pathways relevant in COVID-19 disease

Brief Bioinform. 2021 Mar 22;22(2):1324-1337. doi: 10.1093/bib/bbaa376.

Abstract

To 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.

Keywords: COVID-19; MERS-CoV; RNAseq; SARS-CoV; SARS-CoV-2; coronaviruses; transcriptomics.

MeSH terms

  • COVID-19 / immunology*
  • COVID-19 / virology
  • Gene Expression Profiling*
  • Humans
  • Influenza A virus / immunology
  • Kaplan-Meier Estimate
  • Lung / immunology
  • Lung / virology*
  • Reproducibility of Results
  • SARS-CoV-2 / genetics*