Klopfleisch Robert, Klupp Barbara G, Fuchs Walter, Kopp Martina, Teifke Jens P, Mettenleiter Thomas C
Institute of Molecular Biology, Friedrich-Loeffler-Institut, Boddenblick 5A, D-17493 Greifswald-Insel Riems, Germany.
J Virol. 2006 Jun;80(11):5571-6. doi: 10.1128/JVI.02589-05.
Neurotropism is a distinctive feature of members of the Alphaherpesvirinae. However, its molecular basis remains enigmatic. In the past, research has been focused mainly on the role of viral envelope proteins in modulating herpesvirus neuroinvasion and neurovirulence (T. C. Mettenleiter, Virus Res. 92:192-206, 2003). To further analyze the molecular requirements for neuroinvasion of the alphaherpesvirus pseudorabies virus (PrV), adult mice were infected intranasally with a set of single- or multiple-deletion mutants lacking the UL3, UL4, UL7, UL11, UL13, UL16, UL17, UL21, UL31, UL34, UL37, UL41, UL43, UL46, UL47, UL48, UL51, US3, US9, glycoprotein E (gE), gM, UL11/US9, UL11/UL16, UL16/UL21, UL11/UL16/UL21, UL11/gE, UL11/gM, UL43/gK, UL43/gM, or UL43/gK/gM genes. Neurovirulence was evaluated by measuring mean survival times compared to that after wild-type virus infection. Furthermore, by immunohistochemical detection of infected neurons, the kinetics of viral spread in the murine central nervous system was investigated.
嗜神经性是α疱疹病毒亚科成员的一个显著特征。然而,其分子基础仍然是个谜。过去,研究主要集中在病毒包膜蛋白在调节疱疹病毒神经侵袭和神经毒力中的作用(T.C.梅滕莱特,《病毒研究》92:192 - 206,2003)。为了进一步分析α疱疹病毒伪狂犬病病毒(PrV)神经侵袭的分子要求,成年小鼠经鼻感染了一组缺失UL3、UL4、UL7、UL11、UL13、UL16、UL17、UL21、UL31、UL34、UL37、UL41、UL43、UL46、UL47、UL48、UL51、US3、US9、糖蛋白E(gE)、gM、UL11/US9、UL11/UL16、UL16/UL21、UL11/UL16/UL21、UL11/gE、UL11/gM、UL43/gK、UL43/gM或UL43/gK/gM基因的单缺失或多缺失突变体。通过测量与野生型病毒感染后的平均存活时间相比,评估神经毒力。此外,通过免疫组织化学检测感染的神经元,研究了病毒在小鼠中枢神经系统中的传播动力学。