Lindgren S W, Stojiljkovic I, Heffron F
Department of Microbiology and Immunology, Oregon Health Sciences University, Portland 97201, USA.
Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):4197-201. doi: 10.1073/pnas.93.9.4197.
Phagocytic cells are a critical line of defense against infection. The ability of a pathogen to survive and even replicate within phagocytic cells is a potent method of evading the defense mechanisms of the host. A number of pathogens survive within macrophages after phagocytosis and this contributes to their virulence. Salmonella is one of these pathogens. Here we report that 6-14 hr after Salmonella enters the macrophage and replicates, it resides in large vacuoles and causes the destruction of these cells. Furthermore, we identified four independently isolated MudJ-lacZ insertion mutants that no longer cause the formation of these vacuoles or kill the macrophages. All four insertions were located in the ompR/envZ regulon. These findings suggest that killing and escape from macrophages may be as important steps in Salmonella pathogenesis as are survival and replication in these host cells.
吞噬细胞是抵御感染的关键防线。病原体在吞噬细胞内存活甚至复制的能力是逃避宿主防御机制的有效手段。许多病原体在被吞噬后能在巨噬细胞内存活,这有助于其毒力的发挥。沙门氏菌就是这类病原体之一。在此我们报告,沙门氏菌进入巨噬细胞并复制6 - 14小时后,它存在于大液泡中并导致这些细胞的破坏。此外,我们鉴定出四个独立分离的MudJ - lacZ插入突变体,它们不再导致这些液泡的形成或杀死巨噬细胞。所有四个插入位点都位于ompR/envZ调节子中。这些发现表明,在沙门氏菌致病过程中,杀死并从巨噬细胞中逃逸可能与在这些宿主细胞内存活和复制一样重要。