Nasal mucus-derived KLK13 restricts SARS-CoV-2 infection via proteolytic cleavage of spike
Epithelial cilia directly come into contact with inhaled pathogens. The nasal mucus functions as a formidable barrier against penetration of viral particles. KLK13 is secreted into nasal mucus and efficiently cleaves the spike proteins across different coronavirus species. KLK13-mediated cleavage of spike inhibits SARS-CoV-2 entry and syncytium formation. Intranasally delivered KLK13 also restricts SARS-CoV-2 infection <i>in vivo</i>. The finding that KLK13 acts as a scissor of viral spike in nasal mucus paves the way for the development of new antivirals against respiratory viruses.
Authors
- Ran Chen (ORCID: https://orcid.org/0009-0003-0668-9136)
- Wenying Cao (ORCID: https://orcid.org/0009-0004-3756-1503)
- Shuofeng Yuan (ORCID: https://orcid.org/0000-0001-7996-1119)
- Hehe Cao
- Ningze Zheng
- Jianheng Chen
- Guigen Zhang (ORCID: https://orcid.org/0000-0002-3336-6768)
- Hui Zhang (ORCID: https://orcid.org/0000-0003-3620-610X)
- X. Deng
Institutions
- Sun Yat-sen University (CN)
- Institute of Human Virology (NG)
- University of Hong Kong (HK)
Publication Details
- Journal
- mBio
- Published
- 2025-10-20
- DOI
- https://doi.org/10.1128/mbio.02051-25
- Primary Topic
- SARS-CoV-2 and COVID-19 Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00