Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8) open reading frame 4 protein (Kaposica) is a functional homolog of complement control proteins

被引:50
作者
Mullick, J
Bernet, J
Singh, AK
Lambris, JD
Sahu, A
机构
[1] Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
[2] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
基金
英国惠康基金;
关键词
D O I
10.1128/JVI.77.6.3878-3881.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome analysis of Kaposi's sarcoma-associated herpesvirus (KSHV) has revealed the presence of an open reading frame (ORF 4) with sequence homology to complement control proteins. To assign a function to this protein, we have now expressed this ORF using the Pichia expression system and shown that the purified protein inhibited human complement-mediated lysis of erythrocytes, blocked cell surface deposition of C3b (the proteolytically activated form of C3), and served as a cofactor for factor I-mediated inactivation of complement proteins C3b and C4b (the subunits of C3 convertases). Thus, our data indicate that this KSHV inhibitor of complement activation (kaposica) provides a mechanism by which KSHV can subvert complement attack by the host.
引用
收藏
页码:3878 / 3881
页数:4
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