Original Virucidal activity and mechanism of action of cetylpyridinium chloride against SARS-CoV-2

被引:13
作者
Okamoto, Nako [1 ]
Saito, Akatsuki [2 ,3 ]
Okabayashi, Tamaki [2 ,3 ]
Komine, Akihiko [1 ]
机构
[1] Sunstar Inc, R&D, 1-35-10 Kawanishi Cho, Takatsuki, Osaka 5691133, Japan
[2] Univ Miyazaki, Fac Agr, Dept Vet Sci, Miyazaki, Japan
[3] Univ Miyazaki, Ctr Anim Dis Control, Miyazaki, Japan
关键词
SARS-CoV-2; COVID-19; Antiviral; Virus inactivation; Cetylpyridinium chloride;
D O I
10.1016/j.ajoms.2022.04.001
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the pathogen causing the coronavirus disease 2019 (COVID-19) global pandemic. Recent studies have shown the importance of the throat and salivary glands as sites of virus replication and transmission. The viral host receptor, angio-tensin-converting enzyme 2 (ACE2), is broadly enriched in epithelial cells of the salivary glands and oral mucosae. Oral care products containing cetylpyridinium chloride (CPC) as a bactericidal ingredient are known to exhibit antiviral activity against SARS-CoV-2 in vitro. However, the exact mechanism of action remains unknown. Methods: This study examined the antiviral activity of CPC against SARS-CoV-2 and its inhibitory effect on the interaction between the viral spike (S) protein and ACE2 using an enzyme-linked immunosorbent assay.Results: CPC (0.05%, 0.1% and 0.3%) effectively inactivated SARS-CoV-2 within the contact times (20 and 60 s) in directions for use of oral care products in vitro. The binding ability of both the S protein and ACE2 were reduced by CPC.Conclusions: Our results suggest that CPC inhibits the interaction between S protein and ACE2, and thus, reduces infectivity of SARS-CoV-2 and suppresses viral adsorption.
引用
收藏
页码:800 / 804
页数:5
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