Unité de Recherche et d'Expertise Environnement et Risques Infectieux, Groupe Arbovirus, Institut Pasteur, Paris, France.
Unité de Neuro-Immunologie Virale, Institut Pasteur, Paris, France.
PLoS One. 2021 Jun 4;16(6):e0252595. doi: 10.1371/journal.pone.0252595. eCollection 2021.
Japanese encephalitis virus (JEV) is the major cause of viral encephalitis in South East Asia. It has been suggested that, as a consequence of the inflammatory process during JEV infection, there is disruption of the blood-brain barrier (BBB) tight junctions that in turn allows the virus access to the central nervous system (CNS). However, what happens at early times of JEV contact with the BBB is poorly understood. In the present work, we evaluated the ability of both a virulent and a vaccine strain of JEV (JEV RP9 and SA14-14-2, respectively) to cross an in vitro human BBB model. Using this system, we demonstrated that both JEV RP9 and SA14-14-2 are able to cross the BBB without disrupting it at early times post viral addition. Furthermore, we find that almost 10 times more RP9 infectious particles than SA14-14 cross the model BBB, indicating this BBB model discriminates between the virulent RP9 and the vaccine SA14-14-2 strains of JEV. Beyond contributing to the understanding of early events in JEV neuroinvasion, we demonstrate this in vitro BBB model can be used as a system to study the viral determinants of JEV neuroinvasiveness and the molecular mechanisms by which this flavivirus crosses the BBB during early times of neuroinvasion.
日本脑炎病毒(JEV)是东南亚病毒性脑炎的主要病因。据推测,由于 JEV 感染过程中的炎症反应,血脑屏障(BBB)紧密连接被破坏,病毒由此进入中枢神经系统(CNS)。然而,JEV 与 BBB 早期接触时会发生什么情况尚不清楚。在本研究中,我们评估了两种强毒力和减毒活疫苗株 JEV(JEV RP9 和 SA14-14-2)穿过体外 BBB 模型的能力。使用该系统,我们证明 JEV RP9 和 SA14-14-2 均可在病毒添加后的早期阶段穿过 BBB 而不破坏其完整性。此外,我们发现 RP9 感染性颗粒穿过模型 BBB 的数量比 SA14-14-2 多近 10 倍,表明该 BBB 模型可以区分强毒力的 RP9 和减毒活疫苗 SA14-14-2 株 JEV。除了有助于理解 JEV 神经入侵的早期事件外,我们还证明该体外 BBB 模型可用于研究 JEV 神经入侵的病毒决定因素,以及该黄病毒在神经入侵早期穿过 BBB 的分子机制。