iScience (Jan 2021)

Transcriptomic similarities and differences in host response between SARS-CoV-2 and other viral infections

  • Simone A. Thair,
  • Yudong D. He,
  • Yehudit Hasin-Brumshtein,
  • Suraj Sakaram,
  • Rushika Pandya,
  • Jiaying Toh,
  • David Rawling,
  • Melissa Remmel,
  • Sabrina Coyle,
  • George N. Dalekos,
  • Ioannis Koutsodimitropoulos,
  • Glykeria Vlachogianni,
  • Eleni Gkeka,
  • Eleni Karakike,
  • Georgia Damoraki,
  • Nikolaos Antonakos,
  • Purvesh Khatri,
  • Evangelos J. Giamarellos-Bourboulis,
  • Timothy E. Sweeney

Journal volume & issue
Vol. 24, no. 1
p. 101947

Abstract

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Summary: The pandemic 2019 novel coronavirus disease (COVID-19) shares certain clinical characteristics with other acute viral infections. We studied the whole-blood transcriptomic host response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using RNAseq from 24 healthy controls and 62 prospectively enrolled patients with COVID-19. We then compared these data to non-COVID-19 viral infections, curated from 23 independent studies profiling 1,855 blood samples covering six viruses (influenza, respiratory syncytial virus (RSV), human rhinovirus (HRV), severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1), Ebola, dengue). We show gene expression changes in COVID-19 versus non-COVID-19 viral infections are highly correlated (r = 0.74, p < 0.001). However, we also found 416 genes specific to COVID-19. Inspection of top genes revealed dynamic immune evasion and counter host responses specific to COVID-19. Statistical deconvolution of cell proportions maps many cell type proportions concordantly shifting. Discordantly increased in COVID-19 were CD56bright natural killer cells and M2 macrophages. The concordant and discordant responses mapped out here provide a window to explore the pathophysiology of the host response to SARS-CoV-2.

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