Down-regulation of CD46 by piliated Neisseria gonorrhoeae

被引:37
作者
Gill, DB
Koomey, M
Cannon, KG
Atkinson, JP
机构
[1] Washington Univ, Sch Med, Dept Med, Div Rheumatol, St Louis, MO 63110 USA
[2] Univ Oslo, Ctr Biotechnol, Ctr Mol Biol & Neurosci, N-0316 Oslo, Norway
[3] Univ Oslo, Inst Pharm, Dept Microbiol, N-0316 Oslo, Norway
[4] Univ N Carolina, Sch Med, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
关键词
type IV pilus; PilT; pilus retraction; PilE; protein shedding;
D O I
10.1084/jem.20031159
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human membrane cofactor protein (CD46) protects host cells against complement attack and may function as a receptor for pathogenic Neissniae. We assessed CD46 expression in the human cervical cell line ME-180 after exposure to Neisseria gonorrhoeae. Piliated but not nonpiliated gonococci adhered to cells and produced tip to an 80% reduction in CD46 surface expression by 6 h that persisted for at least 24 h. This response required a minimum multiplicity of infection of 10 and was not prevented by antibodies to CD46. CD46 down-regulation was not attributable to intracellular retention or a global or specific shutdown of mRNA or protein synthesis. Substantial quantities of CD46 were found in the supernatants, indicating a specific shedding of this protein. Adherent gonococci lacking the pilus retraction protein PilT did not down-regulate CD46 but de-repression of pilT expression restored CD46 down-regulation. After experimental infection of human volunteers with a gonococcal variant incapable of inducing CID46 down-regulation, variants of this strain were reisolated that exhibited CD46 down-regulation. Pilus-mediated interactions of gonococci with human epithelial cells results in a pathogen-induced manipulation of the host cell environment in which a membrane protein is removed from epithehal cells by liberation into the surrounding milieu.
引用
收藏
页码:1313 / 1322
页数:10
相关论文
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