Feierbach B, Bisher M, Goodhouse J, Enquist L W
301 Schultz Building, Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
J Virol. 2007 Jul;81(13):6846-57. doi: 10.1128/JVI.00069-07. Epub 2007 Apr 25.
The neurotropic alphaherpesviruses invade and spread in the nervous system in a directional manner between synaptically connected neurons. Until now, this property has been studied only in living animals and has not been accessible to in vitro analysis. In this study, we describe an in vitro system in which cultured peripheral nervous system neurons are separated from their neuron targets by an isolator chamber ring. Using pseudorabies virus (PRV), an alphaherpesvirus capable of transneuronal spread in neural circuits of many animals, we have recapitulated in vitro all known genetic requirements for retrograde and anterograde transneuronal spread as determined previously in vivo. We show that in vitro transneuronal spread requires intact axons and the presence of the viral proteins gE, gI, and Us9. We also show that transneuronal spread is dependent on the viral glycoprotein gB, which is required for membrane fusion, but not on gD, which is required for extracellular spread. We demonstrate ultrastructural differences between anterograde- and retrograde-traveling virions. Finally, we show live imaging of dynamic fluorescent virion components in axons and postsynaptic target neurons.
嗜神经α疱疹病毒在突触连接的神经元之间以定向方式侵入并在神经系统中传播。到目前为止,这一特性仅在活体动物中进行过研究,尚未进行体外分析。在本研究中,我们描述了一种体外系统,其中培养的外周神经系统神经元通过隔离室环与它们的神经元靶标分离。利用伪狂犬病病毒(PRV),一种能够在许多动物的神经回路中进行跨神经元传播的α疱疹病毒,我们在体外重现了先前在体内确定的逆行和顺行跨神经元传播的所有已知遗传要求。我们表明,体外跨神经元传播需要完整的轴突以及病毒蛋白gE、gI和Us9的存在。我们还表明,跨神经元传播依赖于病毒糖蛋白gB,它是膜融合所必需的,但不依赖于细胞外传播所必需的gD。我们展示了顺行和逆行病毒粒子之间的超微结构差异。最后,我们展示了轴突和突触后靶神经元中动态荧光病毒粒子成分的实时成像。