Reich-Slotky Ronit, Kabbash Christina A, Della-Latta Phyllis, Blanchard John S, Feinmark Steven J, Freeman Sherry, Kaplan Gilla, Shuman Howard A, Silverstein Samuel C
Department of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY 10032, USA.
J Bacteriol. 2009 Aug;191(16):5262-71. doi: 10.1128/JB.00175-09. Epub 2009 May 8.
We report here that gemfibrozil (GFZ) inhibits axenic and intracellular growth of Legionella pneumophila and of 27 strains of wild-type and multidrug-resistant Mycobacterium tuberculosis in bacteriological medium and in human and mouse macrophages, respectively. At a concentration of 0.4 mM, GFZ completely inhibited L. pneumophila fatty acid synthesis, while at 0.12 mM it promoted cytoplasmic accumulation of polyhydroxybutyrate. To assess the mechanism(s) of these effects, we cloned an L. pneumophila FabI enoyl reductase homolog that complemented for growth an Escherichia coli strain carrying a temperature-sensitive enoyl reductase and rendered the complemented E. coli strain sensitive to GFZ at the nonpermissive temperature. GFZ noncompetitively inhibited this L. pneumophila FabI homolog, as well as M. tuberculosis InhA and E. coli FabI.
我们在此报告,吉非贝齐(GFZ)分别在细菌培养基以及人和小鼠巨噬细胞中,抑制嗜肺军团菌以及27株野生型和耐多药结核分枝杆菌的无菌生长和细胞内生长。在浓度为0.4 mM时,GFZ完全抑制嗜肺军团菌脂肪酸合成,而在0.12 mM时,它促进聚羟基丁酸酯的细胞质积累。为了评估这些作用的机制,我们克隆了一种嗜肺军团菌FabI烯酰还原酶同源物,该同源物可补充携带温度敏感型烯酰还原酶的大肠杆菌菌株的生长,并使互补的大肠杆菌菌株在非允许温度下对GFZ敏感。GFZ非竞争性抑制这种嗜肺军团菌FabI同源物以及结核分枝杆菌InhA和大肠杆菌FabI。