Jim Kin Ki, Engelen-Lee JooYeon, van der Sar Astrid M, Bitter Wilbert, Brouwer Matthijs C, van der Ende Arie, Veening Jan-Willem, van de Beek Diederik, Vandenbroucke-Grauls Christina M J E
Department of Medical Microbiology and Infection Control, VU University Medical Center, De Boelelaan 1108, 1081 HZ, Amsterdam, The Netherlands.
Department of Neurology, Center of Infection and Immunity Amsterdam (CINIMA), Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
J Neuroinflammation. 2016 Aug 19;13(1):188. doi: 10.1186/s12974-016-0655-y.
Streptococcus pneumoniae is one of the most important causes of bacterial meningitis, an infection where unfavourable outcome is driven by bacterial and host-derived toxins. In this study, we developed and characterized a pneumococcal meningitis model in zebrafish embryos that allows for real-time investigation of early host-microbe interaction.
Zebrafish embryos were infected in the caudal vein or hindbrain ventricle with green fluorescent wild-type S. pneumoniae D39 or a pneumolysin-deficient mutant. The kdrl:mCherry transgenic zebrafish line was used to visualize the blood vessels, whereas phagocytic cells were visualized by staining with far red anti-L-plastin or in mpx:GFP/mpeg1:mCherry zebrafish, that have green fluorescent neutrophils and red fluorescent macrophages. Imaging was performed by fluorescence confocal and time-lapse microscopy.
After infection by caudal vein, we saw focal clogging of the pneumococci in the blood vessels and migration of bacteria through the blood-brain barrier into the subarachnoid space and brain tissue. Infection with pneumolysin-deficient S. pneumoniae in the hindbrain ventricle showed attenuated growth and migration through the brain as compared to the wild-type strain. Time-lapse and confocal imaging revealed that the initial innate immune response to S. pneumoniae in the subarachnoid space mainly consisted of neutrophils and that pneumolysin-mediated cytolytic activity caused a marked reduction of phagocytes.
This new meningitis model permits detailed analysis and visualization of host-microbe interaction in pneumococcal meningitis in real time and is a very promising tool to further our insights in the pathogenesis of pneumococcal meningitis.
肺炎链球菌是细菌性脑膜炎最重要的病因之一,细菌性脑膜炎这种感染的不良后果是由细菌和宿主衍生的毒素驱动的。在本研究中,我们开发并鉴定了一种斑马鱼胚胎肺炎球菌脑膜炎模型,该模型可实时研究早期宿主与微生物的相互作用。
用绿色荧光野生型肺炎链球菌D39或肺炎溶血素缺陷型突变体经尾静脉或后脑脑室感染斑马鱼胚胎。kdrl:mCherry转基因斑马鱼品系用于观察血管,而吞噬细胞则通过用远红抗L- plastin染色或在mpx:GFP/mpeg1:mCherry斑马鱼中观察,后者具有绿色荧光中性粒细胞和红色荧光巨噬细胞。通过荧光共聚焦显微镜和延时显微镜进行成像。
经尾静脉感染后,我们观察到肺炎球菌在血管中局部阻塞,并通过血脑屏障迁移到蛛网膜下腔和脑组织。与野生型菌株相比,后脑脑室感染肺炎溶血素缺陷型肺炎链球菌显示其在脑内的生长和迁移减弱。延时和共聚焦成像显示,蛛网膜下腔对肺炎链球菌的初始固有免疫反应主要由中性粒细胞组成,且肺炎溶血素介导的细胞溶解活性导致吞噬细胞显著减少。
这种新的脑膜炎模型能够实时详细分析和观察肺炎球菌脑膜炎中宿主与微生物的相互作用,是深入了解肺炎球菌脑膜炎发病机制的非常有前景的工具。