Abstract |
Herpes simplex viruses (HSVs) display affinity for cell-surface heparan sulfate proteoglycans with biological relevance in virus entry. Here, we exploit an approach to inhibiting HSV infection by using a sulfated fucoidan, and a guluronic acid-rich alginate derived from Sargassum tenerrimum, mimicking the active domain of the entry receptor. These macromolecules have apparent molecular masses of 30+/-5 and 26+/-5 kDa, respectively. They and their chemically sulfated derivatives showed activity against herpes simplex virus type 1 (HSV-1). Their inhibitory concentration 50% (IC(50)) values were in the range 0.5-15 microg/ml and they lacked cytotoxicity at concentrations up to 1000 microg/ml. The anti-HSV activity increased with increasing sulfate ester content. Our results suggest the feasibility of inhibiting HSV infection by blocking viral entry with polysaccharide having specific structure.
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Authors | Sharmistha Sinha, Akram Astani, Tuhin Ghosh, Paul Schnitzler, Bimalendu Ray |
Journal | Phytochemistry
(Phytochemistry)
Vol. 71
Issue 2-3
Pg. 235-42
(Feb 2010)
ISSN: 1873-3700 [Electronic] England |
PMID | 19931103
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | 2009 Elsevier Ltd. All rights reserved. |
Chemical References |
- Alginates
- Antiviral Agents
- Hexuronic Acids
- Plant Extracts
- Polysaccharides
- guluronic acid
- Glucuronic Acid
- fucoidan
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Topics |
- Alginates
(chemistry, pharmacology, therapeutic use)
- Animals
- Antiviral Agents
(chemistry, pharmacology, therapeutic use)
- Cells, Cultured
- Glucuronic Acid
(chemistry, pharmacology, therapeutic use)
- Haplorhini
- Herpes Simplex
(drug therapy, virology)
- Herpesvirus 1, Human
(drug effects)
- Hexuronic Acids
(chemistry, pharmacology, therapeutic use)
- Inhibitory Concentration 50
- Phytotherapy
- Plant Extracts
(chemistry, pharmacology, therapeutic use)
- Polysaccharides
(chemistry, pharmacology, therapeutic use)
- Sargassum
(chemistry)
- Structure-Activity Relationship
- Virus Integration
(drug effects)
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