Luo Zhao-Qing, Isberg Ralph R
Howard Hughes Medical Institute and Department of Molecular Biology and Microbiology, Tufts University School of Medicine, 150 Harrison Avenue, Boston, MA 02111, USA.
Proc Natl Acad Sci U S A. 2004 Jan 20;101(3):841-6. doi: 10.1073/pnas.0304916101. Epub 2004 Jan 8.
Legionella pneumophila is an intracellular pathogen that multiplies in a specialized vacuole within host cells. Biogenesis of this vacuole requires the Dot/Icm type IV protein translocation system. By using a Cre/loxP-based protein translocation assay, we found that proteins translocated by the Dot/Icm complex across the host phagosomal membrane can also be transferred from one bacterial cell to another. The flexibility of this system allowed the identification of several families of proteins translocated by the Dot/Icm complex. When analyzed by immunofluorescence microscopy, a protein identified by this procedure, SidC, was shown to translocate across the phagosomal membranes to the cytoplasmic face of the L. pneumophila phagosome. The identification of large numbers of these substrates, and the fact that the absence of any one substrate rarely results in strong defects in intracellular growth, indicate that there is significant functional redundancy among the Dot/Icm translocation targets.
嗜肺军团菌是一种细胞内病原体,在宿主细胞内的特殊液泡中繁殖。这种液泡的生物发生需要Dot/Icm IV型蛋白质转运系统。通过使用基于Cre/loxP的蛋白质转运测定法,我们发现Dot/Icm复合物转运穿过宿主吞噬体膜的蛋白质也可以从一个细菌细胞转移到另一个细菌细胞。该系统的灵活性使得能够鉴定出几个由Dot/Icm复合物转运的蛋白质家族。通过免疫荧光显微镜分析,通过该程序鉴定的一种蛋白质SidC被证明可穿过吞噬体膜转运到嗜肺军团菌吞噬体的细胞质面。大量这些底物的鉴定,以及任何一种底物的缺失很少导致细胞内生长出现严重缺陷这一事实,表明Dot/Icm转运靶点之间存在显著的功能冗余。