Bai Fengwei, Town Terrence, Pradhan Deepti, Cox Jonathan, Ledizet Michel, Anderson John F, Flavell Richard A, Krueger Joanna K, Koski Raymond A, Fikrig Erol
Section of Rheumatology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
J Virol. 2007 Feb;81(4):2047-55. doi: 10.1128/JVI.01840-06. Epub 2006 Dec 6.
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.
西尼罗河病毒(WNV)可引发致命的鼠类和人类脑炎。该病毒的包膜蛋白与宿主细胞相互作用。因此,用WNV包膜蛋白对鼠脑cDNA噬菌体展示文库进行筛选,从而鉴定出了几种黏附肽。其中,肽1在体外可阻止WNV感染,其50%抑制浓度为67μM,并且还能抑制相关黄病毒登革病毒的感染。肽9是肽1的衍生物,在体外是一种特别有效的WNV抑制剂,其50%抑制浓度为2.6μM。此外,与对照动物相比,用与肽9孵育过的WNV攻击的小鼠病毒血症和死亡率降低。肽9穿透了鼠血脑屏障并在脑实质中被发现,这意味着它可能在中枢神经系统中具有抗病毒活性。这些短肽为开发针对西尼罗河脑炎以及可能针对其他黄病毒的新疗法奠定了基础。