Department of Microbiology & Immunology, Midwestern University, Downers Grove, IL 60515, USA.
Biochem Biophys Res Commun. 2013 Mar 22;432(4):672-6. doi: 10.1016/j.bbrc.2013.02.020. Epub 2013 Feb 15.
Previously we reported the role of zebrafish (ZF) encoded glucosaminyl 3-O-sulfotransferase-3 (3-OST-3) isoform in assisting herpes simplex virus type-1 (HSV-1) entry and spread by generating an entry receptor to HSV-1 envelope glycoprotein D (gD). However, the ability of ZF encoded 3-OST-2 isoform to participate in HSV-1 entry has not been determined although it is predominantly expressed in ZF brain, a prime target for HSV-1 to infect and establish lifelong latency. Here we report the expression cloning of ZF encoded 3-OST-2 isoform and demonstrate HSV-1 entry into resistant Chinese hamster ovary (CHO-K1) cells expressing the clone. Additional significance of ZF encoded 3-OST-2 receptor was demonstrated using medically important isolates of HSV-1. In addition, interference to HSV-1 entry was observed upon co-expression of HSV-1 gD and ZF 3-OST-2. Similarly HSV-1 entry was significantly inhibited by the pre-treatment of cells with enzyme HS lyases (heparinase II/III). Finally, ZF-3-OST-2 expressing CHO-K1 was able to fuse with HSV-1 glycoprotein expressing cells suggesting their role in HSV-1 spread. Taken together our result demonstrates a role for ZF 3-OST-2 in HSV-1 pathogenesis.
先前我们报道了斑马鱼(ZF)编码的氨基葡糖 3-O-磺基转移酶-3(3-OST-3)同工型在协助单纯疱疹病毒 1 型(HSV-1)进入和传播中的作用,通过产生 HSV-1 包膜糖蛋白 D(gD)的进入受体。然而,尽管 ZF 编码的 3-OST-2 同工型主要在 ZF 大脑中表达,是 HSV-1 感染和建立终身潜伏的主要靶标,但它参与 HSV-1 进入的能力尚未确定。在这里,我们报道了 ZF 编码的 3-OST-2 同工型的表达克隆,并证明了该克隆表达的 CHO-K1 细胞中 HSV-1 的进入。我们还使用具有医学重要性的 HSV-1 分离株证明了 ZF 编码的 3-OST-2 受体的额外意义。此外,在共表达 HSV-1 gD 和 ZF 3-OST-2 时,观察到对 HSV-1 进入的干扰。同样,用酶 HS 裂解酶(肝素酶 II/III)预处理细胞也显著抑制了 HSV-1 的进入。最后,表达 ZF-3-OST-2 的 CHO-K1 能够与表达 HSV-1 糖蛋白的细胞融合,表明它们在 HSV-1 的传播中起作用。总之,我们的结果表明 ZF 3-OST-2 在 HSV-1 发病机制中起作用。