» Articles » PMID: 36754974

Potential Antiviral Effects of Pantethine Against SARS-CoV-2

Overview
Journal Sci Rep
Specialty Science
Date 2023 Feb 8
PMID 36754974
Authors
Affiliations
Soon will be listed here.
Abstract

SARS-CoV-2 interacts with cellular cholesterol during many stages of its replication cycle. Pantethine was reported to reduce total cholesterol levels and fatty acid synthesis and potentially alter different processes that might be involved in the SARS-CoV-2 replication cycle. Here, we explored the potential antiviral effects of pantethine in two in vitro experimental models of SARS-CoV-2 infection, in Vero E6 cells and in Calu-3a cells. Pantethine reduced the infection of cells by SARS-CoV-2 in both preinfection and postinfection treatment regimens. Accordingly, cellular expression of the viral spike and nucleocapsid proteins was substantially reduced, and we observed a significant reduction in viral copy numbers in the supernatant of cells treated with pantethine. In addition, pantethine inhibited the infection-induced increase in TMPRSS2 and HECT E3 ligase expression in infected cells as well as the increase in antiviral interferon-beta response and inflammatory gene expression in Calu-3a cells. Our results demonstrate that pantethine, which is well tolerated in humans, was very effective in controlling SARS-CoV-2 infection and might represent a new therapeutic drug that can be repurposed for the prevention or treatment of COVID-19 and long COVID syndrome.

Citing Articles

Cholesterol and Cholesterol-Lowering Medications in COVID-19-An Unresolved Matter.

Grewal T, Nguyen M, Buechler C Int J Mol Sci. 2024; 25(19).

PMID: 39408818 PMC: 11477656. DOI: 10.3390/ijms251910489.


Cholesterol and COVID-19-therapeutic opportunities at the host/virus interface during cell entry.

Grewal T, Nguyen M, Buechler C Life Sci Alliance. 2024; 7(5).

PMID: 38388172 PMC: 10883773. DOI: 10.26508/lsa.202302453.

References
1.
Bajimaya S, Frankl T, Hayashi T, Takimoto T . Cholesterol is required for stability and infectivity of influenza A and respiratory syncytial viruses. Virology. 2017; 510:234-241. PMC: 5571833. DOI: 10.1016/j.virol.2017.07.024. View

2.
Neufeldt C, Cerikan B, Cortese M, Frankish J, Lee J, Plociennikowska A . SARS-CoV-2 infection induces a pro-inflammatory cytokine response through cGAS-STING and NF-κB. Commun Biol. 2022; 5(1):45. PMC: 8755718. DOI: 10.1038/s42003-021-02983-5. View

3.
Yuan Z, Hu B, Xiao H, Tan X, Li Y, Tang K . The E3 Ubiquitin Ligase RNF5 Facilitates SARS-CoV-2 Membrane Protein-Mediated Virion Release. mBio. 2022; 13(1):e0316821. PMC: 8805027. DOI: 10.1128/mbio.03168-21. View

4.
Dai J, Wang H, Liao Y, Tan L, Sun Y, Song C . Coronavirus Infection and Cholesterol Metabolism. Front Immunol. 2022; 13:791267. PMC: 9069556. DOI: 10.3389/fimmu.2022.791267. View

5.
Novelli G, Liu J, Biancolella M, Alonzi T, Novelli A, Patten J . Inhibition of HECT E3 ligases as potential therapy for COVID-19. Cell Death Dis. 2021; 12(4):310. PMC: 7987752. DOI: 10.1038/s41419-021-03513-1. View