Antiviral peptides targeting the west nile virus envelope protein

被引:84
作者
Bai, Fengwei
Town, Terrence
Pradhan, Deepti
Cox, Jonathan
Ashish
Ledizet, Michel
Anderson, John F.
Flavell, Richard A.
Krueger, Joanna K.
Koski, Raymond A.
Fikrig, Erol
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Sect Rheumatol,Anlyan Ctr Med Res & Educ, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[4] Univ N Carolina, Dept Chem, Charlotte, NC 28213 USA
[5] L2 Diagnost, New Haven, CT 06511 USA
[6] Connecticut Agr Expt Stn, Dept Entomol, New Haven, CT 06504 USA
关键词
D O I
10.1128/JVI.01840-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 mu M 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 mu M. 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.
引用
收藏
页码:2047 / 2055
页数:9
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