O'Donnell Christopher D, Shukla Deepak
Department of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.
Virol Sin. 2008 Dec 1;23(6):383-393. doi: 10.1007/s12250-008-2992-1.
Herpes simplex virus type-1 (HSV-1) is one of many pathogens that use the cell surface glycosaminoglycan heparan sulfate as a receptor. Heparan sulfate is highly expressed on the surface and extracellular matrix of virtually all cell types making it an ideal receptor. Heparan sulfate interacts with HSV-1 envelope glycoproteins gB and gC during the initial attachment step during HSV-1 entry. In addition, a modified form of heparan sulfate, known as 3-O-sulfated heparan sulfate, interacts with HSV-1 gD to induce fusion between the viral envelope and host cell membrane. The 3-O-sulfation of heparan sulfate is a rare modification which occurs during the biosynthesis of heparan sulfate that is carried out by a family of enzymes known as 3-O-sulfotransferases. Due to its involvement in multiple steps of the infection process, heparan sulfate has been a prime target for the development of agents to inhibit HSV entry. Understanding how heparan sulfate functions during HSV-1 infection may not only be critical for inhibiting infection by this virus, but it may also be crucial in the fight against many other pathogens as well.
单纯疱疹病毒1型(HSV-1)是众多利用细胞表面糖胺聚糖硫酸乙酰肝素作为受体的病原体之一。硫酸乙酰肝素在几乎所有细胞类型的表面和细胞外基质中都高度表达,使其成为理想的受体。在HSV-1进入的初始附着步骤中,硫酸乙酰肝素与HSV-1包膜糖蛋白gB和gC相互作用。此外,一种硫酸乙酰肝素的修饰形式,即3-O-硫酸化硫酸乙酰肝素,与HSV-1 gD相互作用,诱导病毒包膜与宿主细胞膜融合。硫酸乙酰肝素的3-O-硫酸化是一种罕见的修饰,发生在由一类称为3-O-磺基转移酶的酶进行的硫酸乙酰肝素生物合成过程中。由于其参与感染过程的多个步骤,硫酸乙酰肝素一直是开发抑制HSV进入药物的主要靶点。了解硫酸乙酰肝素在HSV-1感染过程中的作用方式,不仅对于抑制这种病毒的感染至关重要,而且在对抗许多其他病原体的斗争中也可能至关重要。