| Literature DB >> 17151121 |
Fengwei Bai1, Terrence Town, Deepti Pradhan, Jonathan Cox, Michel Ledizet, John F Anderson, Richard A Flavell, Joanna K Krueger, Raymond A Koski, Erol Fikrig.
Abstract
West Nile virus (WNV) can cause fatal murine and human encephalitis. The viral envelope protein interacts with host cells. A murine brain cDNA phage display library was therefore probed with WNV envelope protein, resulting in the identification of several adherent peptides. Of these, peptide 1 prevented WNV infection in vitro with a 50% inhibition concentration of 67 muM and also inhibited infection of a related flavivirus, dengue virus. Peptide 9, a derivative of peptide 1, was a particularly potent inhibitor of WNV in vitro, with a 50% inhibition concentration of 2.6 muM. Moreover, mice challenged with WNV that had been incubated with peptide 9 had reduced viremia and fatality compared with control animals. Peptide 9 penetrated the murine blood-brain barrier and was found in the brain parenchyma, implying that it may have antiviral activity in the central nervous system. These short peptides serve as the basis for developing new therapeutics for West Nile encephalitis and, potentially, other flaviviruses.Entities:
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Year: 2006 PMID: 17151121 PMCID: PMC1797586 DOI: 10.1128/JVI.01840-06
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103