Ohara Shinya, Sota Yasuhiro, Sato Sho, Tsutsui Ken-Ichiro, Iijima Toshio
Division of Systems Neuroscience, Tohoku University Graduate School of Life Sciences, Sendai, Japan.
PLoS One. 2017 Jul 10;12(7):e0180960. doi: 10.1371/journal.pone.0180960. eCollection 2017.
Viral vectors that can infect neurons transsynaptically and can strongly express foreign genes are useful for investigating the organization of neural circuits. We previously developed a propagation-competent rabies virus (RV) vector based on a highly attenuated HEP-Flury strain (rHEP5.0-CVSG), which selectively infects neurons and propagates between synaptically connected neurons in a retrograde direction. Its relatively low level of transgene expression, however, makes immunostaining necessary to visualize the morphological features of infected neurons. To increase the transgene expression level of this RV vector, in this study we focused on two viral proteins: the large protein (L) and matrix protein (M). We first attempted to enhance the expression of L, which is a viral RNA polymerase, by deleting the extra transcription unit and shortening the intergenic region between the G and L genes. This viral vector (rHEP5.0-GctL) showed increased transgene expression level with efficient transsynaptic transport. We next constructed an RV vector with a rearranged gene order (rHEP5.0-GML) with the aim to suppress the expression of M, which plays a regulatory role in virus RNA synthesis. Although this vector showed high transgene expression level, the efficiency of transsynaptic transport was low. To further evaluate the usability of rHEP5.0-GctL as a transsynaptic tracer, we inserted a fluorescent timer as a transgene, which changes the color of its fluorescence from blue to red over time. This viral vector enabled us the differentiation of primary infected neurons from secondary infected neurons in terms of the fluorescence wavelength. We expect this propagation-competent RV vector to be useful for elucidating the complex organization of the central nervous system.
能够跨突触感染神经元并能强烈表达外源基因的病毒载体,对于研究神经回路的组织结构很有用。我们之前基于高度减毒的HEP-Flury株(rHEP5.0-CVSG)开发了一种具有传播能力的狂犬病病毒(RV)载体,该载体选择性感染神经元,并在突触连接的神经元之间逆行传播。然而,其相对较低水平的转基因表达使得需要进行免疫染色才能观察到被感染神经元的形态特征。为了提高这种RV载体的转基因表达水平,在本研究中我们聚焦于两种病毒蛋白:大蛋白(L)和基质蛋白(M)。我们首先尝试通过删除额外的转录单元并缩短G基因和L基因之间的基因间隔区来增强L(一种病毒RNA聚合酶)的表达。这种病毒载体(rHEP5.0-GctL)显示出转基因表达水平提高且具有高效的跨突触运输能力。接下来,我们构建了一种基因顺序重排的RV载体(rHEP5.0-GML),目的是抑制在病毒RNA合成中起调节作用的M的表达。尽管这种载体显示出高转基因表达水平,但跨突触运输效率较低。为了进一步评估rHEP5.0-GctL作为跨突触示踪剂的可用性,我们插入了一个荧光定时器作为转基因,其荧光颜色会随时间从蓝色变为红色。这种病毒载体使我们能够根据荧光波长区分初级感染神经元和次级感染神经元。我们期望这种具有传播能力的RV载体可用于阐明中枢神经系统的复杂组织结构。