Sirard J C, Guidi-Rontani C, Fouet A, Mock M
Unité des Toxines et Pathogénie Bactériennes, URA 1858 du CNRS, Institut Pasteur, Paris, France.
Int J Med Microbiol. 2000 Oct;290(4-5):313-6. doi: 10.1016/S1438-4221(00)80030-2.
The germination of spores within the host is the initial step of anthrax infection. We have shown, using immunofluorescence staining, confocal scanning laser microscopy and image cytometry analysis, that the alveolar macrophage is the primary site of B. anthracis germination in a murine inhalation infection model. B. anthracis germinated inside macrophages, in vesicles derived from the phagosomal compartment. We have demonstrated that the toxin genes and their trans-activator, AtxA, are expressed within the macrophages after germination. It was also shown that the pXO1 plasmid strongly enhanced capsule formation and that this influence is mediated by AtxA. This indicates the existence of a regulon where AtxA is the regulatory protein acting on genes located on different plasmids. We identified a tricistronic germination operon gerX located between the pag and atxA genes on the 40-kb toxin-encoding fragment of pXO1 . Analysis of a gerX null mutant indicated that gerX-encoded proteins are involved in the virulence of B. anthracis.
孢子在宿主体内萌发是炭疽感染的起始步骤。我们运用免疫荧光染色、共聚焦扫描激光显微镜及图像细胞仪分析表明,在小鼠吸入感染模型中,肺泡巨噬细胞是炭疽芽孢杆菌萌发的主要部位。炭疽芽孢杆菌在巨噬细胞内、源自吞噬体区室的囊泡中萌发。我们已证实,毒素基因及其反式激活因子AtxA在萌发后于巨噬细胞内表达。还表明pXO1质粒强烈增强荚膜形成,且这种影响由AtxA介导。这表明存在一个操纵子,其中AtxA是作用于位于不同质粒上基因的调节蛋白。我们在pXO1的40 kb毒素编码片段上位于pag和atax基因之间鉴定出一个三顺反子萌发操纵子gerX。对gerX缺失突变体的分析表明,gerX编码的蛋白参与炭疽芽孢杆菌的毒力。