Conway Michael J, Watson Alan M, Colpitts Tonya M, Dragovic Srdjan M, Li Zhiyong, Wang Penghua, Feitosa Fabiana, Shepherd Denueve T, Ryman Kate D, Klimstra William B, Anderson John F, Fikrig Erol
Department of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, Connecticut, USA.
J Virol. 2014 Jan;88(1):164-75. doi: 10.1128/JVI.02235-13. Epub 2013 Oct 16.
Dengue virus (DENV), a flavivirus of global importance, is transmitted to humans by mosquitoes. In this study, we developed in vitro and in vivo models of saliva-mediated enhancement of DENV infectivity. Serine protease activity in Aedes aegypti saliva augmented virus infectivity in vitro by proteolyzing extracellular matrix proteins, thereby increasing viral attachment to heparan sulfate proteoglycans and inducing cell migration. A serine protease inhibitor reduced saliva-mediated enhancement of DENV in vitro and in vivo, marked by a 100-fold reduction in DENV load in murine lymph nodes. A saliva-mediated infectivity enhancement screen of fractionated salivary gland extracts identified serine protease CLIPA3 as a putative cofactor, and short interfering RNA knockdown of CLIPA3 in mosquitoes demonstrated its role in influencing DENV infectivity. Molecules in mosquito saliva that facilitate viral infectivity in the vertebrate host provide novel targets that may aid in the prevention of disease.
登革病毒(DENV)是一种具有全球重要性的黄病毒,通过蚊子传播给人类。在本研究中,我们建立了唾液介导增强DENV感染性的体外和体内模型。埃及伊蚊唾液中的丝氨酸蛋白酶活性通过蛋白水解细胞外基质蛋白增强了体外病毒感染性,从而增加病毒与硫酸乙酰肝素蛋白聚糖的附着并诱导细胞迁移。一种丝氨酸蛋白酶抑制剂在体外和体内均降低了唾液介导的DENV增强作用,其标志是小鼠淋巴结中DENV载量降低100倍。对唾液腺提取物分级进行的唾液介导感染性增强筛选确定丝氨酸蛋白酶CLIPA3为假定的辅助因子,在蚊子中对CLIPA3进行短干扰RNA敲低证明了其在影响DENV感染性中的作用。蚊子唾液中促进脊椎动物宿主中病毒感染性的分子提供了可能有助于预防疾病的新靶点。