tetano
Editor, Senior Moderator
Cell Rep
. 2021 Jan 12;34(2):108628.
doi: 10.1016/j.celrep.2020.108628.
MDA5 Governs the Innate Immune Response to SARS-CoV-2 in Lung Epithelial Cells
Xin Yin[SUP] 1 [/SUP], Laura Riva[SUP] 2 [/SUP], Yuan Pu[SUP] 2 [/SUP], Laura Martin-Sancho[SUP] 2 [/SUP], Jun Kanamune[SUP] 3 [/SUP], Yuki Yamamoto[SUP] 3 [/SUP], Kouji Sakai[SUP] 4 [/SUP], Shimpei Gotoh[SUP] 3 [/SUP], Lisa Miorin[SUP] 5 [/SUP], Paul D De Jesus[SUP] 2 [/SUP], Chih-Cheng Yang[SUP] 6 [/SUP], Kristina M Herbert[SUP] 2 [/SUP], Sunnie Yoh[SUP] 2 [/SUP], Judd F Hultquist[SUP] 7 [/SUP], Adolfo Garc?a-Sastre[SUP] 8 [/SUP], Sumit K Chanda[SUP] 9 [/SUP]
Affiliations
Abstract
Recent studies have profiled the innate immune signatures in patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and suggest that cellular responses to viral challenge may affect disease severity. Yet the molecular events that underlie cellular recognition and response to SARS-CoV-2 infection remain to be elucidated. Here, we find that SARS-CoV-2 replication induces a delayed interferon (IFN) response in lung epithelial cells. By screening 16 putative sensors involved in sensing of RNA virus infection, we found that MDA5 and LGP2 primarily regulate IFN induction in response to SARS-CoV-2 infection. Further analyses revealed that viral intermediates specifically activate the IFN response through MDA5-mediated sensing. Additionally, we find that IRF3, IRF5, and NF-κB/p65 are the key transcription factors regulating the IFN response during SARS-CoV-2 infection. In summary, these findings provide critical insights into the molecular basis of the innate immune recognition and signaling response to SARS-CoV-2.
Keywords: IRF3; IRF5; MDA5; NF-κB/p65; SARS-CoV-2; interferon; lung epithelial cells.
. 2021 Jan 12;34(2):108628.
doi: 10.1016/j.celrep.2020.108628.
MDA5 Governs the Innate Immune Response to SARS-CoV-2 in Lung Epithelial Cells
Xin Yin[SUP] 1 [/SUP], Laura Riva[SUP] 2 [/SUP], Yuan Pu[SUP] 2 [/SUP], Laura Martin-Sancho[SUP] 2 [/SUP], Jun Kanamune[SUP] 3 [/SUP], Yuki Yamamoto[SUP] 3 [/SUP], Kouji Sakai[SUP] 4 [/SUP], Shimpei Gotoh[SUP] 3 [/SUP], Lisa Miorin[SUP] 5 [/SUP], Paul D De Jesus[SUP] 2 [/SUP], Chih-Cheng Yang[SUP] 6 [/SUP], Kristina M Herbert[SUP] 2 [/SUP], Sunnie Yoh[SUP] 2 [/SUP], Judd F Hultquist[SUP] 7 [/SUP], Adolfo Garc?a-Sastre[SUP] 8 [/SUP], Sumit K Chanda[SUP] 9 [/SUP]
Affiliations
- PMID: 33440148
- DOI: 10.1016/j.celrep.2020.108628
Abstract
Recent studies have profiled the innate immune signatures in patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and suggest that cellular responses to viral challenge may affect disease severity. Yet the molecular events that underlie cellular recognition and response to SARS-CoV-2 infection remain to be elucidated. Here, we find that SARS-CoV-2 replication induces a delayed interferon (IFN) response in lung epithelial cells. By screening 16 putative sensors involved in sensing of RNA virus infection, we found that MDA5 and LGP2 primarily regulate IFN induction in response to SARS-CoV-2 infection. Further analyses revealed that viral intermediates specifically activate the IFN response through MDA5-mediated sensing. Additionally, we find that IRF3, IRF5, and NF-κB/p65 are the key transcription factors regulating the IFN response during SARS-CoV-2 infection. In summary, these findings provide critical insights into the molecular basis of the innate immune recognition and signaling response to SARS-CoV-2.
Keywords: IRF3; IRF5; MDA5; NF-κB/p65; SARS-CoV-2; interferon; lung epithelial cells.