Echoviruses and Coxsackie B viruses that use human decay-accelerating factor (DAF) as a receptor do not bind the rodent analogues of DAF

被引:36
作者
Spiller, OB
Goodfellow, IG
Evans, DJ
Almond, JW
Morgan, BP
机构
[1] Cardiff Univ, Dept Med Biochem, Complement Biol Grp, Cardiff CF4 4XX, S Glam, Wales
[2] Univ Glasgow, Inst Virol, Glasgow G11 5JR, Lanark, Scotland
[3] Univ Reading, Sch Anim & Microbial Sci, Virol Grp, Reading RG6 2AJ, Berks, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1086/315210
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Many serotypes of echovirus (EV) and Coxsackie B virus (CBV) bind human decay-accelerating factor (DAF) and use it as a receptor for infection, Analogues for DAF have been isolated from mice and rats and characterized; these analogues have amino acid identities to human DAF of similar to 60%, EV serotypes 3, 6', 7, 11-13, and 29 and CBV serotypes 1, 3, and 5 caused hemagglutination of human erythrocytes but not rat or mouse erythrocytes, suggesting failure to bind rodent DAF. To confirm this evidence, radiolabeled viruses were incubated with transfected Chinese hamster ovary (CHO) cells that were abundantly expressing each type of DAF. Only cells that expressed human DAF bound virus, Although binding of EV and CBV was specific for human DAF, complement inhibition by DAF expressed in CHO cells was similar for each analogue.
引用
收藏
页码:340 / 343
页数:4
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