School of Molecular and Biomedical Science, University of Adelaide, Adelaide, South Australia, Australia.
PLoS One. 2013 Dec 19;8(12):e84975. doi: 10.1371/journal.pone.0084975. eCollection 2013.
Shigella flexneri remains a significant human pathogen due to high morbidity among children < 5 years in developing countries. One of the key features of Shigella infection is the ability of the bacterium to initiate actin tail polymerisation to disseminate into neighbouring cells. Dynamin II is associated with the old pole of the bacteria that is associated with F-actin tail formation. Dynamin II inhibition with dynasore as well as siRNA knockdown significantly reduced Shigella cell to cell spreading in vitro. The ocular mouse Sereny model was used to determine if dynasore could delay the progression of Shigella infection in vivo. While dynasore did not reduce ocular inflammation, it did provide significant protection against weight loss. Therefore dynasore's effects in vivo are unlikely to be related to the inhibition of cell spreading observed in vitro. We found that dynasore decreased S. flexneri-induced HeLa cell death in vitro which may explain the protective effect observed in vivo. These results suggest the administration of dynasore or a similar compound during Shigella infection could be a potential intervention strategy to alleviate disease symptoms.
福氏志贺菌由于在发展中国家 5 岁以下儿童中的发病率较高,仍然是一种重要的人类病原体。志贺氏菌感染的一个关键特征是细菌能够启动肌动蛋白尾聚合,从而扩散到邻近的细胞。动力蛋白 II 与细菌的旧极相关,该极与 F-肌动蛋白尾的形成有关。用 dynasore 抑制动力蛋白 II 以及 siRNA 敲低显著减少了体外志贺氏菌的细胞间传播。在眼部小鼠 Sereny 模型中,研究人员确定 dynasore 是否可以延缓体内志贺氏菌感染的进展。虽然 dynasore 并没有减轻眼部炎症,但它确实对体重减轻提供了显著的保护。因此,dynasore 在体内的作用不太可能与体外观察到的细胞扩散抑制有关。研究人员发现 dynasore 降低了福氏志贺菌诱导的 HeLa 细胞体外死亡,这可能解释了体内观察到的保护作用。这些结果表明,在志贺氏菌感染期间给予 dynasore 或类似化合物可能是减轻疾病症状的一种潜在干预策略。