Abstract
We recently described the discovery, genome, clinical features, genotypes and evolution of a novel and global human respiratory virus named human coronavirus HKU1 (HCoV-HKU1) which is not yet culturable. We expressed a C-terminal FLAG-tagged CoV-HKU1 spike (S) protein by the Semliki Forest Virus (SFV) system and investigated its maturation profile. Pulse chase labeling revealed that S-FLAG was expressed as high-mannose N-glycans of monomers and trimers. It was predominantly cleaved into subdomains S1 and S2 during maturation. S1 was secreted into the medium. Immunofluorescence analysis visualized S along the secretory pathway from endoplasmic reticulum to plasma membrane. Cleavage of S and release of HCoV-HKU1 S pseudotyped virus were inhibited by furin or furin-like enzyme inhibitors. The cell-based expressed full-length S-FLAG could be recognized by the convalescent serum obtained from a patient with HCoV-HKU1 pneumonia. The data suggest that the native form of HCoV-HKU1 spike expressed in our system can be used in developing serological diagnostic assay and in understanding the role of S in the viral life cycle.
Original language | English |
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Pages (from-to) | 1527-1536 |
Number of pages | 10 |
Journal | Experimental Biology and Medicine |
Volume | 233 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2008 |
Externally published | Yes |
ASJC Scopus Subject Areas
- General Biochemistry,Genetics and Molecular Biology
Keywords
- Coronavirus HKU1
- Furin inhibitor
- Glycoprotein
- Life cycle
- Maturation
- Native conformation
- Nglycosylation
- Seroepidemiology
- Spike
- Surface expression
- Virus maturation