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Zebrafish-Encoded 3- O -Sulfotransferase-3 Isoform Mediates Herpes Simplex Virus Type 1 Entry and Spread
Zebrafish (2010)
  • Kevin S Jones, Howard University
Abstract
Heparan sulfate proteoglycans modified by human glucosaminyl 3-O-sulfotransferase-3 (3-OST-3) isoform generates the cellular receptor for herpes simplex virus type 1 (HSV-1). Interestingly, the ability of zebrafish (ZF)-encoded 3-OST-3 isoform to modify heparan sulfate to mediate HSV-1 entry and cell-cell fusion has not been determined although it is predominantly expressed in ZF, a popular model organism to study viral infections. Here, we demonstrate that expression of ZF-encoded 3-OST-3 isoform renders the resistant Chinese hamster ovary (CHO-K1) cells to become susceptible for HSV-1 entry. The following lines of evidence support the important role of ZF-encoded 3-OST-3 isoform as the mediator of HSV-1 entry into CHO-K1 cells: (1) ZF 3-OST-3-expressing CHO-K1 cells were able to preferentially bind HSV-1 glycoprotein D, and (2) CHO-K1 cells expressing ZF-encoded 3-OST-3 acquire the ability to fuse with cells expressing HSV-1 glycoproteins. Finally, knocking down 3-OST-3 receptor by siRNA in ZF fibroblasts cells significantly reduced HSV-1 entry and glycoprotein D binding to cells. Taken together, our results provide novel insight into the significance of ZF 3-OST-3 isoform as an HSV-1 entry and fusion receptor and its potential involvement in the HSV-1 disease model of ZF.
Disciplines
Publication Date
May, 2010
DOI
10.1089/zeb.2009.0621
Citation Information
Kevin S Jones. "Zebrafish-Encoded 3- O -Sulfotransferase-3 Isoform Mediates Herpes Simplex Virus Type 1 Entry and Spread" Zebrafish Vol. 7 Iss. 2 (2010) p. 181 - 187
Available at: http://works.bepress.com/kevin-jones/6/