Severe Acute Respiratory Syndrome Coronavirus Open Reading Frame (ORF) 3b, ORF 6, and Nucleocapsid Proteins Function as Interferon Antagonists
Icahn School of Medicine at Mount Sinai · University of North Carolina at Chapel Hill
Abstract
The severe acute respiratory syndrome coronavirus (SARS-CoV) is highly pathogenic in humans, with a death rate near 10%. This high pathogenicity suggests that SARS-CoV has developed mechanisms to overcome the host innate immune response. It has now been determined that SARS-CoV open reading frame (ORF) 3b, ORF 6, and N proteins antagonize interferon, a key component of the innate immune response. All three proteins inhibit the expression of beta interferon (IFN-beta), and further examination revealed that these SARS-CoV proteins inhibit a key protein necessary for the expression of IFN-beta, IRF-3. N protein dramatically inhibited expression from an NF-kappaB-responsive promoter. All three proteins were able…
Citation impact
- FWCI
- 11.39
- Percentile
- 100%
- References
- 33
Authors
5- SASarah A. Kopecky-Bromberg
Icahn School of Medicine at Mount Sinai
- LMLuis Martínez‐Sobrido
Icahn School of Medicine at Mount Sinai
- MBMatthew B. Frieman
University of North Carolina at Chapel Hill
- RARalph A. Baric
University of North Carolina at Chapel Hill
- PPPeter PaleseCorresponding
Icahn School of Medicine at Mount Sinai
Topics & keywords
- Biology
- Open reading frame
- Interferon
- Sendai virus
- STAT1
- Innate immune system
- Virology
- Coronavirus
- Good health and well-being