Low-molecular weight mannogalactofucans prevent herpes simplex virus type 1 infection via activation of Toll-like receptor 2
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
28522392
DOI
10.1016/j.ijbiomac.2017.05.060
PII: S0141-8130(16)33044-6
Knihovny.cz E-resources
- Keywords
- Antiviral activity, Mannogalactofucans, Toll-like receptor 2,
- MeSH
- Antiviral Agents chemistry pharmacology MeSH
- Chlorocebus aethiops MeSH
- Galactose chemistry pharmacology MeSH
- Herpes Simplex metabolism prevention & control MeSH
- Herpesvirus 1, Human drug effects MeSH
- Molecular Weight MeSH
- Solubility MeSH
- Toll-Like Receptor 2 metabolism MeSH
- Vero Cells MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antiviral Agents MeSH
- Galactose MeSH
- Toll-Like Receptor 2 MeSH
Low-molecular-weight mannogalactofucans (LMMGFs, <4000g/mol) were prepared by the enzymatic degradation of Undaria pinnatifida sporophyll galactofucan (MF) and evaluated or their antiviral activities and underlying action mechanisms against herpes simplex virus type 1 (HSV-1). The 50% inhibitory concentrations (IC50) of LMMGFs and MF were 2.64 and 2.42μg/mL, respectively. LMMGFs inhibited the viral entry on the host cell surface and also exhibited inhibitory activity directly against viral particles, as observed in a virucidal assay. LMMGFs dose-dependently enhanced the mRNA expression of Toll-like receptor 2 (TLR2) and stimulated the phosphorylation of Akt and JNK in Vero cells. These results clearly demonstrated that LMMGFs use TLR2 as their receptor, preventing HSV-1 infection on the host cell surface and antagonizing viral adsorption via TLR2 pathway activation in Vero cells.
Department of Biotechnology The Catholic University of Korea Bucheon Gyeonggi do 14662 Korea
Department of Microbiology College of Medicine Kon Kuk University Seoul 05029 Korea
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