PT  - JOURNAL ARTICLE
AU  - Daniel Blanco-Melo
AU  - Benjamin E. Nilsson-Payant
AU  - Wen-Chun Liu
AU  - Rasmus Møller
AU  - Maryline Panis
AU  - David Sachs
AU  - Randy A. Albrecht
AU  - Benjamin R. tenOever
TI  - SARS-CoV-2 launches a unique transcriptional signature from in vitro, ex vivo, and in vivo systems
AID  - 10.1101/2020.03.24.004655
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.03.24.004655
4099  - http://biorxiv.org/content/early/2020/03/24/2020.03.24.004655.short
4100  - http://biorxiv.org/content/early/2020/03/24/2020.03.24.004655.full
AB  - One of the greatest threats to humanity is the emergence of a pandemic virus. Among those with the greatest potential for such an event include influenza viruses and coronaviruses. In the last century alone, we have observed four major influenza A virus pandemics as well as the emergence of three highly pathogenic coronaviruses including SARS-CoV-2, the causative agent of the ongoing COVID-19 pandemic. As no effective antiviral treatments or vaccines are presently available against SARS-CoV-2, it is important to understand the host response to this virus as this may guide the efforts in development towards novel therapeutics. Here, we offer the first in-depth characterization of the host transcriptional response to SARS-CoV-2 and other respiratory infections through in vitro, ex vivo, and in vivo model systems. Our data demonstrate the each virus elicits both core antiviral components as well as unique transcriptional footprints. Compared to the response to influenza A virus and respiratory syncytial virus, SARS-CoV-2 elicits a muted response that lacks robust induction of a subset of cytokines including the Type I and Type III interferons as well as a numerous chemokines. Taken together, these data suggest that the unique transcriptional signature of this virus may be responsible for the development of COVID-19.