COXSACKIEVIRUSES B1, B3, AND B5 USE DECAY-ACCELERATING FACTOR AS A RECEPTOR FOR CELL ATTACHMENT

被引:229
作者
SHAFREN, DR
BATES, RC
AGREZ, MV
HERD, RL
BURNS, GF
BARRY, RD
机构
[1] UNIV NEWCASTLE,FAC MED,DEPT MICROBIOL,NEWCASTLE,NSW 2300,AUSTRALIA
[2] UNIV NEWCASTLE,FAC MED,CANC RES UNIT,NEWCASTLE,NSW 2300,AUSTRALIA
[3] UNIV NEWCASTLE,FAC MED,DEPT SURG SCI,NEWCASTLE,NSW 2300,AUSTRALIA
关键词
D O I
10.1128/JVI.69.6.3873-3877.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Receptor binding and subsequent cell-mediated internalization or disassembly are the initial steps in virus replication. Cell surface molecules that participate in this process are the primary determinants of virus tissue tropism. Monoclonal antibody blockade, immunoprecipitation, and DNA transfection were used to identify decay accelerating factor as a major cell attachment receptor for coxsackieviruses B1, B3, and B5. However, expression of human decay acceleration factor on the surface of nonpermissive murine fibroblasts led only to virus attachment without subsequent replication, and it was concluded that an additional cellular cofactor(s) is required to facilitate cell entry and subsequent replication.
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页码:3873 / 3877
页数:5
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