Gaillard J L, Jaubert F, Berche P
Laboratoire de Microbiologie, Institut National de la Sante et de la Recherche Medicale, Paris, France.
J Exp Med. 1996 Feb 1;183(2):359-69. doi: 10.1084/jem.183.2.359.
The intracellular parasite Listeria monocytogenes is able to induce its internalization by cultured mammalian cells that are not normally phagocytic. This process requires the expression of the chromosomal locus inlAB. We studied the virulence of an inlAB mutant and of its parent in murine listeriosis. Irrespective of the route of inoculation, the inlAB mutant was severely attenuated for growth in the liver. The livers of mice inoculated with the inlAB mutant displayed much smaller infectious foci than the parent as early as 24 h after infection. Electron microscopy showed that these foci consisted of a few inflammatory cells, with few bacteria; bacteria were rarely found within hepatocytes. In contrast, foci in livers of mice inoculated with the parent consisted of islets of heavily infected hepatocytes that were infiltrated by numerous neutrophils; bacteria seemed intact within hepatocytes and damaged within neutrophils. A direct role of inlAB for the entry of L. monocytogenes into hepatocytes was confirmed in a cell infection system using the murine embryonic hepatocyte cell line TIB73. The inlAB mutant was approximately 20-fold less invasive in trans. The "invasion locus" inlAB contributes to protect L. monocytogenes from the host's innate defense mechanisms by promoting its entry into hepatocytes.
细胞内寄生菌单核细胞增生李斯特菌能够诱导非吞噬性培养哺乳动物细胞将其内化。此过程需要染色体位点inlAB的表达。我们研究了inlAB突变体及其亲本在小鼠李斯特菌病中的毒力。无论接种途径如何,inlAB突变体在肝脏中的生长均严重减弱。接种inlAB突变体的小鼠肝脏,早在感染后24小时,其感染灶就比亲本小得多。电子显微镜显示,这些病灶由少量炎症细胞组成,细菌很少;在肝细胞内很少发现细菌。相比之下,接种亲本的小鼠肝脏中的病灶由大量受感染的肝细胞小岛组成,这些小岛被大量中性粒细胞浸润;细菌在肝细胞内似乎完好无损,而在中性粒细胞内则受到损伤。在使用小鼠胚胎肝细胞系TIB73的细胞感染系统中,证实了inlAB对单核细胞增生李斯特菌进入肝细胞具有直接作用。inlAB突变体的侵袭性比野生型低约20倍。“侵袭位点”inlAB通过促进单核细胞增生李斯特菌进入肝细胞,有助于保护其免受宿主先天防御机制的影响。