Cleavage of group 1 coronavirus spike proteins: How furin cleavage is traded off against heparan sulfate binding upon cell culture adaptation

被引:79
作者
de Haan, C. A. M. [1 ]
Haijema, B. J. [1 ]
Schellen, P. [1 ]
Schreur, P. Wichgers [1 ]
Lintelo, E. Te [1 ]
Vennema, H. [1 ]
Rottier, P. J. M. [1 ]
机构
[1] Univ Utrecht, Fac Vet Med, Dept Immunol & Infect Dis, Div Virol, NL-3584 CL Utrecht, Netherlands
关键词
D O I
10.1128/JVI.00074-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A longstanding enigmatic feature of the group 1 coronaviruses is the uncleaved phenotype of their spike protein, an exceptional property among class I fusion proteins. Here, however, we show that some group 1 coronavirus spike proteins carry a furin enzyme recognition motif and can actually be cleaved, as demonstrated for a feline coronavirus. Interestingly, this feature can be lost during cell culture adaptation by a single mutation in the cleavage motif, this, however, preserves a heparan sulfate binding motif and renders infection by the virus heparan sulfate dependent. We identified a similar cell culture adaptation for the human coronavirus OC43.
引用
收藏
页码:6078 / 6083
页数:6
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