4.4 Article

Syndecan-1 and syndecan-2 play key roles in herpes simplex virus type-1 infection

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JOURNAL OF GENERAL VIROLOGY
卷 92, 期 -, 页码 733-743

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SOC GENERAL MICROBIOLOGY
DOI: 10.1099/vir.0.027052-0

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  1. NIH [AI057860, AI081869, AI050050]
  2. Rosztoczy Foundation
  3. [EY01792]

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Herpes simplex virus type 1 (HSV-1) is an important human pathogen and a leading cause of infectious blindness in the developed world. HSV-1 exploits heparan sulfate proteoglycans (HSPG) for attachment to cells. While the significance of heparan sulphate (HS) moieties in HSV-1 infection is well established, the role of specific proteoglycan core proteins in the infection process remains poorly understood. The objective of this study was to assess the roles of syndecan-1 and syndecan-2 core proteins in HSV-1 infection, both of which are expressed by many HSV-1 target cell types. Our results demonstrate that syndecan-1 and syndecan-2 gene silencing by RNA interference reduces HSV-1 entry, plaque formation and facilitates cell survival. Furthermore, HSV-1 infection increases syndecan-1 and syndecan-2 protein synthesis and a resultant increase in cell surface expression of HS. Our observations suggest that changes in syndecan-1 and syndecan-2 expression levels may be related to active viral infection. Taken together, our findings provide new insights into HSPG functions during HSV-1 entry and spread.

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