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本文引用的文献

1
Transneuronal labeling of a nociceptive pathway, the spino-(trigemino-)parabrachio-amygdaloid, in the rat.大鼠中伤害性感受通路——脊髓(三叉)臂旁核-杏仁核通路的跨神经元标记
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Interconnected parallel circuits between rat nucleus accumbens and thalamus revealed by retrograde transynaptic transport of pseudorabies virus.伪狂犬病病毒逆行跨突触运输揭示大鼠伏隔核与丘脑之间的相互连接平行回路
J Neurosci. 1997 Mar 15;17(6):2143-67. doi: 10.1523/JNEUROSCI.17-06-02143.1997.
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Anterograde, transneuronal transport of herpes simplex virus type 1 strain H129 in the murine visual system.单纯疱疹病毒1型H129株在小鼠视觉系统中的顺行性跨神经元运输。
J Virol. 1996 Aug;70(8):5405-13. doi: 10.1128/JVI.70.8.5405-5413.1996.
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Efferent projections of the anterior perirhinal cortex in the rat.大鼠前梨状周围皮质的传出投射
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Glycoprotein D-negative pseudorabies virus can spread transneuronally via direct neuron-to-neuron transmission in its natural host, the pig, but not after additional inactivation of gE or gI.糖蛋白D阴性伪狂犬病病毒在其自然宿主猪体内可通过直接的神经元到神经元的传递进行跨神经元传播,但在gE或gI进一步失活后则不能。
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Deletion of glycoprotein gE reduces the propagation of pseudorabies virus in the nervous system of mice after intranasal inoculation.糖蛋白gE的缺失降低了鼻内接种后伪狂犬病病毒在小鼠神经系统中的传播。
Virology. 1996 May 1;219(1):279-84. doi: 10.1006/viro.1996.0247.
7
Role of essential glycoproteins gII and gp50 in transneuronal transfer of pseudorabies virus from the hypoglossal nerves of mice.必需糖蛋白gII和gp50在伪狂犬病病毒从小鼠舌下神经进行跨神经元转移中的作用。
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8
Specific pseudorabies virus infection of the rat visual system requires both gI and gp63 glycoproteins.大鼠视觉系统的特异性伪狂犬病病毒感染需要gI和gp63糖蛋白。
J Virol. 1993 Jul;67(7):3786-97. doi: 10.1128/JVI.67.7.3786-3797.1993.
9
Glycoprotein gp50-negative pseudorabies virus: a novel approach toward a nonspreading live herpesvirus vaccine.糖蛋白gp50阴性伪狂犬病病毒:一种开发非传播性活疱疹病毒疫苗的新方法。
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10
Envelope glycoprotein gp50 of pseudorabies virus is essential for virus entry but is not required for viral spread in mice.伪狂犬病病毒的包膜糖蛋白gp50对病毒进入至关重要,但对病毒在小鼠体内的传播并非必需。
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脑内注射两株伪狂犬病病毒后神经元感染的不同模式

Different patterns of neuronal infection after intracerebral injection of two strains of pseudorabies virus.

作者信息

Card J P, Levitt P, Enquist L W

机构信息

Department of Neuroscience, University of Pittsburgh, Pennsylvania 15260, USA.

出版信息

J Virol. 1998 May;72(5):4434-41. doi: 10.1128/JVI.72.5.4434-4441.1998.

DOI:10.1128/JVI.72.5.4434-4441.1998
PMID:9557737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC109677/
Abstract

Pseudorabies virus (PRV), a swine neurotropic alphaherpesvirus, is known to invade the central nervous system (CNS) of a variety of animal species through peripherally projecting axons, replicate in the parent neurons, and then pass transsynaptically to infect other neurons of a circuit. Studies of the human pathogen herpes simplex virus type 1 have reported differences in the direction of transport of two strains of this virus after direct injection into the primate motor cortex. In the present study we examined the direction of transport of virulent and attenuated strains of PRV, utilizing injections into the rat prefrontal cortex to evaluate specific movement of virus through CNS circuitry. The data demonstrate strain-dependent patterns of infection consistent with bidirectional (anterograde and retrograde) transport of virulent virus and unidirectional (retrograde) transport of attenuated PRV from the site of injection. The distribution of infected neurons and the extent of transsynaptic passage also suggest that a release defect in the attenuated strain reduces the apparent rate of viral transport through neuronal circuitry. Finally, injection of different concentrations of virus influenced the onset of replication within a neural circuit. Taken together, these data suggest that viral envelope glycoproteins and virus concentration at the site of injection are important determinants of the rate and direction of viral transport through a multisynaptic circuit in the CNS.

摘要

伪狂犬病病毒(PRV)是一种嗜神经性猪α疱疹病毒,已知它可通过外周投射轴突侵入多种动物物种的中枢神经系统(CNS),在亲代神经元中复制,然后通过突触传递感染回路中的其他神经元。对人类病原体单纯疱疹病毒1型的研究报告称,将该病毒的两株毒株直接注入灵长类动物运动皮层后,其运输方向存在差异。在本研究中,我们通过向大鼠前额叶皮层注射病毒,来评估病毒通过中枢神经系统回路的特定运动,从而研究PRV强毒株和弱毒株的运输方向。数据表明,感染模式具有毒株依赖性,与强毒病毒的双向(顺行和逆行)运输以及弱毒PRV从注射部位的单向(逆行)运输一致。被感染神经元的分布和突触传递的程度还表明,弱毒株中的释放缺陷降低了病毒通过神经元回路的表观运输速率。最后,注射不同浓度的病毒会影响神经回路内复制的起始时间。综上所述,这些数据表明,病毒包膜糖蛋白和注射部位的病毒浓度是决定病毒通过中枢神经系统多突触回路运输速率和方向的重要因素。