Castro-Garza Jorge, King C Harold, Swords W Edward, Quinn Frederick D
División de Biología Celular y Molecular, Centro de Investigación Biomédica del Noreste, IMSS, Monterrey, N.L., Mexico.
FEMS Microbiol Lett. 2002 Jul 2;212(2):145-9. doi: 10.1111/j.1574-6968.2002.tb11258.x.
We developed an in vitro tissue-culture model to analyze the process involved in mycobacterial spread through lung epithelial cell monolayers. A549 cells were infected with low numbers of viable Mycobacterium tuberculosis bacilli expressing the gfp gene. Subsequent addition of a soft agarose overlay prevented the dispersal of the bacilli from the initial points of attachment. By fluorescence microscopy the bacteria were observed to infect and grow within the primary target cells; this was followed by lysis of the infected cells and subsequent infection of adjacent cells. This process repeated itself until an area of clearing (plaque formation) was observed. The addition of amikacin after initial infection did not prevent intracellular growth; however, subsequent plaque formation was not observed. Plaque formation was also observed after infection with Mycobacterium bovis BCG bacilli, but the plaques were smaller than those formed after infection with M. tuberculosis. These observations reinforce the possibility that cell-to-cell spreading of M. tuberculosis bacilli, particularly early in the course of infection within lung macrophages, pneumocytes, and other cells, may be an important component in the infectious process.
我们建立了一种体外组织培养模型,以分析分枝杆菌通过肺上皮细胞单层扩散的过程。用少量表达绿色荧光蛋白(gfp)基因的活结核分枝杆菌感染A549细胞。随后添加软琼脂覆盖物可防止杆菌从初始附着点扩散。通过荧光显微镜观察到细菌在主要靶细胞内感染并生长;接着受感染细胞裂解,随后感染相邻细胞。这个过程不断重复,直到观察到一个清亮区域(噬菌斑形成)。初始感染后添加阿米卡星并不能阻止细胞内生长;然而,随后未观察到噬菌斑形成。用牛分枝杆菌卡介苗感染后也观察到了噬菌斑形成,但这些噬菌斑比结核分枝杆菌感染后形成的噬菌斑小。这些观察结果进一步证实了结核分枝杆菌在细胞间传播的可能性,特别是在肺巨噬细胞、肺细胞和其他细胞感染过程的早期,可能是感染过程中的一个重要组成部分。