Nsp1 facilitates SARS-CoV-2 replication through calcineurin-NFAT signaling.

Autor:	Lui W-Y; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong., Ong CP; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong., Cheung P-HH; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong., Ye Z-W; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong., Chan C-P; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong., To KK-W; Department of Microbiology, The University of Hong Kong, Pokfulam, Hong Kong., Yuen K-S; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong.; School of Nursing, Tung Wah College, Kowloon, Hong Kong., Jin D-Y; School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong.
Jazyk:	angličtina
Zdroj:	MBio [mBio] 2024 Apr 10; Vol. 15 (4), pp. e0039224. Date of Electronic Publication: 2024 Feb 27.
DOI:	10.1128/mbio.00392-24
Abstrakt:	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. Importance: Cyclosporine 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. Competing Interests: The authors declare no conflict of interest.
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu