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吩噻嗪类通过靶向刺突蛋白抑制 SARS-CoV-2 进入。

Phenothiazines Inhibit SARS-CoV-2 Entry through Targeting Spike Protein.

机构信息

Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou 510005, China.

State Key Laboratory of Respiratory Disease, Guangzhou Medical University, Guangzhou 511400, China.

出版信息

Viruses. 2023 Jul 31;15(8):1666. doi: 10.3390/v15081666.


DOI:10.3390/v15081666
PMID:37632009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10458444/
Abstract

Novel coronavirus disease 2019 (COVID-19), a respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has brought an unprecedented public health crisis and continues to threaten humanity due to the persistent emergence of new variants. Therefore, developing more effective and broad-spectrum therapeutic and prophylactic drugs against infection by SARS-CoV-2 and its variants, as well as future emerging CoVs, is urgently needed. In this study, we screened several US FDA-approved drugs and identified phenothiazine derivatives with the ability to potently inhibit the infection of pseudotyped SARS-CoV-2 and distinct variants of concern (VOCs), including B.1.617.2 (Delta) and currently circulating Omicron sublineages XBB and BQ.1.1, as well as pseudotyped SARS-CoV and MERS-CoV. Mechanistic studies suggested that phenothiazines predominantly inhibited SARS-CoV-2 pseudovirus (PsV) infection at the early stage and potentially bound to the spike (S) protein of SARS-CoV-2, which may prevent the proteolytic cleavage of the S protein, thereby exhibiting inhibitory activity against SARS-CoV-2 infection. In summary, our findings suggest that phenothiazines can serve as a potential broad-spectrum therapeutic drug for the treatment of SARS-CoV-2 infection as well as the infection of future emerging human coronaviruses (HCoVs).

摘要

新型冠状病毒病 2019(COVID-19)是一种由严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)引起的呼吸道疾病,由于新变种的持续出现,它带来了前所未有的公共卫生危机,继续威胁着人类。因此,迫切需要开发针对 SARS-CoV-2 及其变体以及未来出现的 CoV 的更有效和广谱的治疗和预防感染的药物。在这项研究中,我们筛选了几种美国食品和药物管理局(FDA)批准的药物,并鉴定出具有抑制假型 SARS-CoV-2 以及包括 B.1.617.2(Delta)在内的不同关注变体(VOCs)、目前流行的奥密克戎亚系 XBB 和 BQ.1.1 以及假型 SARS-CoV 和 MERS-CoV 感染的有效能力的吩噻嗪衍生物。机制研究表明,吩噻嗪类药物主要在早期抑制 SARS-CoV-2 假病毒(PsV)感染,并且可能与 SARS-CoV-2 的刺突(S)蛋白结合,这可能阻止 S 蛋白的蛋白水解裂解,从而对 SARS-CoV-2 感染表现出抑制活性。总之,我们的研究结果表明,吩噻嗪类药物可以作为一种潜在的广谱治疗药物,用于治疗 SARS-CoV-2 感染以及未来出现的人类冠状病毒(HCoV)感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/c18e4c23e9d1/viruses-15-01666-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/1167e3611df2/viruses-15-01666-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/3eddf42aace2/viruses-15-01666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/a47a949be282/viruses-15-01666-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/bb95024f618a/viruses-15-01666-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/c18e4c23e9d1/viruses-15-01666-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/1167e3611df2/viruses-15-01666-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/3eddf42aace2/viruses-15-01666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/a47a949be282/viruses-15-01666-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/bb95024f618a/viruses-15-01666-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f6/10458444/c18e4c23e9d1/viruses-15-01666-g004.jpg

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SynDRep: a synergistic partner prediction tool based on knowledge graph for drug repurposing.

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[2]
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[3]
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[4]
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[5]
NSP6 inhibits the production of ACE2-containing exosomes to promote SARS-CoV-2 infectivity.

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本文引用的文献

[1]
Phenothiazines inhibit SARS-CoV-2 cell entry via a blockade of spike protein binding to neuropilin-1.

Antiviral Res. 2023-1

[2]
A guide to COVID-19 antiviral therapeutics: a summary and perspective of the antiviral weapons against SARS-CoV-2 infection.

FEBS J. 2024-4

[3]
Chemically Modified Bovine β-Lactoglobulin as a Broad-Spectrum Influenza Virus Entry Inhibitor with the Potential to Combat Influenza Outbreaks.

Viruses. 2022-9-16

[4]
Pan-coronavirus fusion inhibitors to combat COVID-19 and other emerging coronavirus infectious diseases.

J Med Virol. 2023-1

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SARS-CoV-2's Variants of Concern: A Brief Characterization.

Front Immunol. 2022

[6]
Inhibition of dengue virus infection by trifluoperazine.

Arch Virol. 2022-11

[7]
Novel cleavage sites identified in SARS-CoV-2 spike protein reveal mechanism for cathepsin L-facilitated viral infection and treatment strategies.

Cell Discov. 2022-6-6

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Effectiveness of Paxlovid in Reducing Severe Coronavirus Disease 2019 and Mortality in High-Risk Patients.

Clin Infect Dis. 2023-2-8

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Glycopeptide Antibiotic Teicoplanin Inhibits Cell Entry of SARS-CoV-2 by Suppressing the Proteolytic Activity of Cathepsin L.

Front Microbiol. 2022-4-28

[10]
Remdesivir and three other drugs for hospitalised patients with COVID-19: final results of the WHO Solidarity randomised trial and updated meta-analyses.

Lancet. 2022-5-21

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