Theodoropoulos C, Wong T H, O'Brien M, Stenzel D
School of Life Sciences, Queensland University of Technology, Brisbane, Queensland 4001, Australia.
Infect Immun. 2001 Apr;69(4):2260-9. doi: 10.1128/IAI.69.4.2260-2269.2001.
This study provides the first definitive evidence that the gram-negative bacterium Plesiomonas shigelloides adheres to and enters eukaryotic intestinal host cells in vitro. P. shigelloides is increasingly regarded as an emerging enteric pathogen and has been implicated in intestinal and extraintestinal infections in humans. However, the establishment of its true role in enteric disease has been hindered by inadequacies in experimental design, deficiencies in clinical diagnosis, and the lack of an appropriate animal model. In this investigation, an in vitro system was used to evaluate plesiomonad pathogenesis. Differentiated epithelium-derived Caco-2 cell monolayers inoculated apically with 12 isolates of P. shigelloides from clinical (intestinal) origins were examined at high resolution using transmission electron microscopy. Bacterial cells were observed adhering to intact microvilli and to the plasma membrane on both the apical and the basal surfaces of the monolayer. The bacteria entered the Caco-2 cells and were observed enclosed in single and multiple membrane-bound vacuoles within the host cell cytoplasm. This observation suggests that initial uptake may occur through a phagocytic-like process, as has been documented for many other enteropathogens. P. shigelloides also was noted free in the cytosol of Caco-2 cells, suggesting escape from cytoplasmic vacuoles. Differences in invasion phenotypes were revealed, suggesting the possibility that, like Escherichia coli, P. shigelloides comprises different pathogenic phenotypes.
本研究提供了首个确凿证据,表明革兰氏阴性菌类志贺邻单胞菌在体外能够黏附并进入真核肠道宿主细胞。类志贺邻单胞菌越来越被视为一种新兴的肠道病原体,并与人类的肠道和肠道外感染有关。然而,由于实验设计不完善、临床诊断不足以及缺乏合适的动物模型,其在肠道疾病中真正作用的确定受到了阻碍。在本研究中,使用体外系统评估邻单胞菌的致病机制。用透射电子显微镜在高分辨率下检查了经顶端接种来自临床(肠道)来源的12株类志贺邻单胞菌的分化上皮衍生的Caco-2细胞单层。观察到细菌细胞黏附在单层细胞顶端和基底表面的完整微绒毛以及质膜上。细菌进入Caco-2细胞,并观察到其被包裹在宿主细胞质内的单个和多个膜结合空泡中。这一观察结果表明,初始摄取可能通过类似吞噬的过程发生,正如许多其他肠道病原体所记录的那样。还注意到类志贺邻单胞菌在Caco-2细胞的胞质溶胶中游离,表明其从细胞质空泡中逸出。揭示了侵袭表型的差异,这表明类志贺邻单胞菌可能像大肠杆菌一样,包含不同的致病表型。