Chen Wangxue, Kuolee Rhonda, Austin John W, Shen Hua, Che Yanming, Conlan J Wayne
Institute for Biological Sciences, National Research Council Canada, 100 Sussex Drive, Ottawa, Ont., Canada K1A 0R6.
Microb Pathog. 2005 Nov-Dec;39(5-6):189-96. doi: 10.1016/j.micpath.2005.08.005. Epub 2005 Oct 28.
Francisella tularensis is a gram-negative facultative intracellular bacterium and the causative agent of tularemia. Two subspecies (type A and B strains) of the pathogen exist, the former being much more virulent than the latter for humans and other higher mammals. In this study, we examined the effect of virulent strains of F. tularensis infection on the thymus and thymocytes and the potential mechanisms involved. Low-dose aerosol exposure of C57BL/6 mice with type A, but not type B, F. tularensis caused severe reduction in thymus weight and destruction of thymocytes, particularly CD4+CD8+ thymocytes, by day 4 after infection. The depletion of thymocytes was accompanied by a significant increase in circulating cortisone levels and could be partially prevented by adrenalectomy. Moreover, thymus atrophy and thymocyte depletion following infection were abolished in mice deficient in tumor necrosis factor receptors 1 and 2, but not in FasL-deficient mice. The severe destruction of the thymus and selective depletion of immature thymocytes during type A F. tularensis infection may represent a key pathogenic mechanism in tularemia and could hinder the development of an effective primary immune response against this highly virulent pathogen.
土拉弗朗西斯菌是一种革兰氏阴性兼性胞内细菌,也是兔热病的病原体。该病原体存在两个亚种(A 型和 B 型菌株),前者对人类和其他高等哺乳动物的毒性比后者强得多。在本研究中,我们检测了土拉弗朗西斯菌强毒株感染对胸腺和胸腺细胞的影响以及其中涉及的潜在机制。用 A 型土拉弗朗西斯菌而非 B 型土拉弗朗西斯菌对 C57BL/6 小鼠进行低剂量气溶胶暴露,在感染后第 4 天导致胸腺重量严重减轻以及胸腺细胞,尤其是 CD4+CD8+胸腺细胞的破坏。胸腺细胞的耗竭伴随着循环皮质酮水平的显著升高,并且肾上腺切除术可部分预防这种情况。此外,在缺乏肿瘤坏死因子受体 1 和 2 的小鼠中,感染后胸腺萎缩和胸腺细胞耗竭被消除,但在 FasL 缺陷小鼠中并未消除。在 A 型土拉弗朗西斯菌感染期间胸腺的严重破坏和未成熟胸腺细胞的选择性耗竭可能代表兔热病的关键致病机制,并且可能阻碍针对这种高毒力病原体的有效初级免疫反应的发展。