tetano
Editor, Senior Moderator
mBio
. 2024 Feb 27:e0039224.
doi: 10.1128/mbio.00392-24. Online ahead of print. Nsp1 facilitates SARS-CoV-2 replication through calcineurin-NFAT signaling
Wai-Yin Lui[SUP] 1 [/SUP], Chon Phin Ong[SUP] 1 [/SUP], Pak-Hin Hinson Cheung[SUP] 1 [/SUP], Zi-Wei Ye[SUP] 1 [/SUP], Chi-Ping Chan[SUP] 1 [/SUP], Kelvin Kai-Wang To[SUP] 2 [/SUP], Kit-San Yuen[SUP] 1 3 [/SUP], Dong-Yan Jin[SUP] 1 [/SUP]
Affiliations
SARS-CoV-2, the causative agent of COVID-19, has been intensely studied in search of effective antiviral treatments. The immunosuppressant cyclosporine A (CsA) has been suggested to be a pan-coronavirus inhibitor, yet its underlying mechanism remained largely unknown. Here, we found that non-structural protein 1 (Nsp1) of SARS-CoV-2 usurped CsA-suppressed nuclear factor of activated T cells (NFAT) signaling to drive the expression of cellular DEAD-box helicase 5 (DDX5), which facilitates viral replication. Nsp1 interacted with calcineurin A (CnA) to displace the regulatory protein regulator of calcineurin 3 (RCAN3) of CnA for NFAT activation. The influence of NFAT activation on SARS-CoV-2 replication was also validated by using the Nsp1-deficient mutant virus. Calcineurin inhibitors, such as CsA and VIVIT, inhibited SARS-CoV-2 replication and exhibited synergistic antiviral effects when used in combination with nirmatrelvir. Our study delineated the molecular mechanism of CsA-mediated inhibition of SARS-CoV-2 replication and the anti-SARS-CoV-2 action of calcineurin inhibitors.IMPORTANCECyclosporine A (CsA), commonly used to inhibit immune responses, is also known to have anti-SARS-CoV-2 activity, but its mode of action remains elusive. Here, we provide a model to explain how CsA antagonizes SARS-CoV-2 through three critical proteins: DDX5, NFAT1, and Nsp1. DDX5 is a cellular facilitator of SARS-CoV-2 replication, and NFAT1 controls the production of DDX5. Nsp1 is a viral protein absent from the mature viral particle and capable of activating the function of NFAT1 and DDX5. CsA and similar agents suppress Nsp1, NFAT1, and DDX5 to exert their anti-SARS-CoV-2 activity either alone or in combination with Paxlovid.
Keywords: DDX5; NFAT; Nsp1; RCAN3; SARS-CoV-2; calcineurin.
. 2024 Feb 27:e0039224.
doi: 10.1128/mbio.00392-24. Online ahead of print. Nsp1 facilitates SARS-CoV-2 replication through calcineurin-NFAT signaling
Wai-Yin Lui[SUP] 1 [/SUP], Chon Phin Ong[SUP] 1 [/SUP], Pak-Hin Hinson Cheung[SUP] 1 [/SUP], Zi-Wei Ye[SUP] 1 [/SUP], Chi-Ping Chan[SUP] 1 [/SUP], Kelvin Kai-Wang To[SUP] 2 [/SUP], Kit-San Yuen[SUP] 1 3 [/SUP], Dong-Yan Jin[SUP] 1 [/SUP]
Affiliations
- PMID: 38411085
- DOI: 10.1128/mbio.00392-24
SARS-CoV-2, the causative agent of COVID-19, has been intensely studied in search of effective antiviral treatments. The immunosuppressant cyclosporine A (CsA) has been suggested to be a pan-coronavirus inhibitor, yet its underlying mechanism remained largely unknown. Here, we found that non-structural protein 1 (Nsp1) of SARS-CoV-2 usurped CsA-suppressed nuclear factor of activated T cells (NFAT) signaling to drive the expression of cellular DEAD-box helicase 5 (DDX5), which facilitates viral replication. Nsp1 interacted with calcineurin A (CnA) to displace the regulatory protein regulator of calcineurin 3 (RCAN3) of CnA for NFAT activation. The influence of NFAT activation on SARS-CoV-2 replication was also validated by using the Nsp1-deficient mutant virus. Calcineurin inhibitors, such as CsA and VIVIT, inhibited SARS-CoV-2 replication and exhibited synergistic antiviral effects when used in combination with nirmatrelvir. Our study delineated the molecular mechanism of CsA-mediated inhibition of SARS-CoV-2 replication and the anti-SARS-CoV-2 action of calcineurin inhibitors.IMPORTANCECyclosporine A (CsA), commonly used to inhibit immune responses, is also known to have anti-SARS-CoV-2 activity, but its mode of action remains elusive. Here, we provide a model to explain how CsA antagonizes SARS-CoV-2 through three critical proteins: DDX5, NFAT1, and Nsp1. DDX5 is a cellular facilitator of SARS-CoV-2 replication, and NFAT1 controls the production of DDX5. Nsp1 is a viral protein absent from the mature viral particle and capable of activating the function of NFAT1 and DDX5. CsA and similar agents suppress Nsp1, NFAT1, and DDX5 to exert their anti-SARS-CoV-2 activity either alone or in combination with Paxlovid.
Keywords: DDX5; NFAT; Nsp1; RCAN3; SARS-CoV-2; calcineurin.