Bello Chakir, Cohen-Salmon Martine, Van Nhieu Guy Tran
Team Intercellular Communication and Microbial Infections, Center for Interdisciplinary, Research in Biology, Collège de France, 75005 Paris, France.
Institut National de la Santé et de la Recherche Médicale U1050, 75005 Paris, France.
Bio Protoc. 2021 Dec 5;11(23):e4242. doi: 10.21769/BioProtoc.4242.
Pneumococcal (PN) meningitis is a life-threatening disease with high mortality rates that leads to permanent neurological sequelae. Studies of the process of bacterial crossing of the blood brain barrier (BBB) are hampered by the lack of relevant and models of meningitis that recapitulate the human disease. PN meningitis involves bacterial access to the bloodstream preceding translocation across the BBB. A large number of PN meningitis models have been developed in mice, with intravenous administration via the lateral tail vein representing the main way to study BBB crossing by PN. While in humans, meningitis is not always associated with bacteremia, PN meningitis after intravenous injection in mice usually develops following sustained and very high bacteremic titers. High grade bacteremia, however, is known to favor inflammation and BBB permeabilization, thereby increasing PN translocation across the BBB and associated damages. Therefore, specific processes associated with early events of PN translocation may be blurred by overall changes in the inflammatory environment and potentially systemic dysfunction in the case of severe sepsis. Here, we report a mouse meningitis model induced by PN injection in the retro-orbital (RO) sinus. We show that, in this model, mice appear to control bacteremic levels during the first 13 h post-infection, while PN crossing of the BBB can be clearly detected by fluorescence confocal microscopy analysis of brain slices as early as 6 h post-infection. Because of the low frequency of events, however, PN translocation across brain parenchymal vessels at early time points requires a rigorous and systematic examination of the brain volume.
肺炎球菌性(PN)脑膜炎是一种危及生命的疾病,死亡率很高,并会导致永久性神经后遗症。由于缺乏能够重现人类疾病的相关脑膜炎模型,对细菌穿越血脑屏障(BBB)过程的研究受到了阻碍。PN脑膜炎涉及细菌在穿越BBB之前进入血液循环。已经在小鼠中开发了大量PN脑膜炎模型,通过侧尾静脉进行静脉注射是研究PN穿越BBB的主要方式。然而在人类中,脑膜炎并不总是与菌血症相关,而小鼠静脉注射后的PN脑膜炎通常在持续且非常高的菌血症滴度后发生。然而,已知高等级菌血症有利于炎症和BBB通透性增加,从而增加PN穿越BBB及相关损伤。因此,在严重脓毒症情况下,PN易位早期事件相关的特定过程可能会被炎症环境的整体变化以及潜在的全身功能障碍所掩盖。在此,我们报告一种通过在眶后(RO)窦注射PN诱导的小鼠脑膜炎模型。我们表明,在该模型中,小鼠在感染后的前13小时似乎能够控制菌血症水平,而早在感染后6小时,通过对脑切片进行荧光共聚焦显微镜分析就可以清楚地检测到PN穿越BBB。然而,由于事件发生频率较低,早期时间点PN在脑实质血管中的易位需要对脑体积进行严格而系统的检查。