journal article Open Access Sep 13, 2024

Chitosan-Modified AgNPs Efficiently Inhibit Swine Coronavirus-Induced Host Cell Infections via Targeting the Spike Protein

Biomolecules Vol. 14 No. 9 pp. 1152 · MDPI AG
View at Publisher Save 10.3390/biom14091152
Abstract
The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has filled a gap in our knowledge regarding the prevention of CoVs. Swine coronavirus (CoV) is a significant pathogen that causes huge economic losses to the global swine industry. Until now, anti-CoV prevention and control have been challenging due to the rapidly generated variants. Silver nanoparticles (AgNPs) with excellent antimicrobial activity have attracted great interest for biosafety prevention and control applications. In this study, we synthesized chitosan-modified AgNPs (Chi-AgNPs) with good biocompatibility to investigate their antiviral effects on swine CoVs. In vitro assays showed that Chi-AgNPs could significantly impaired viral entry. The direct interaction between Chi-AgNPs and CoVs can destroy the viral surface spike (S) protein secondary structure associated with viral membrane fusion, which is caused by the cleavage of disulfide bonds in the S protein. Moreover, the mechanism showed that Chi-AgNPs reduced the virus-induced apoptosis of Vero cells via the ROS/p53 signaling activation pathway. Our data suggest that Chi-AgNPs can serve as a preventive strategy for CoVs infection and provide a molecular basis for the viricidal effect of Chi-AgNPs on CoVs.
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Details
Published
Sep 13, 2024
Vol/Issue
14(9)
Pages
1152
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Funding
National Natural Science Foundation of China Award: 2023M741130
China Postdoctoral Science Foundation Award: 2023M741130
Hunan Provincial Natural Science Foundation of China Award: 2023M741130
Hunan Province Technology Breakthrough Project Award: 2023M741130
Cite This Article
Dongliang Wang, Caiyun Yin, Yihan Bai, et al. (2024). Chitosan-Modified AgNPs Efficiently Inhibit Swine Coronavirus-Induced Host Cell Infections via Targeting the Spike Protein. Biomolecules, 14(9), 1152. https://doi.org/10.3390/biom14091152