Lehrstuhl für Biochemie, Technische Universität München, D-85747 Garching, Germany.
Nat Rev Microbiol. 2010 Jun;8(6):401-12. doi: 10.1038/nrmicro2351. Epub 2010 May 10.
New technologies such as high-throughput methods and 13C-isotopologue-profiling analysis are beginning to provide us with insight into the in vivo metabolism of microorganisms, especially in the host cell compartments that are colonized by intracellular bacterial pathogens. In this Review, we discuss the recent progress made in determining the major carbon sources and metabolic pathways used by model intracellular bacterial pathogens that replicate either in the cytosol or in vacuoles of infected host cells. Furthermore, we highlight the possible links between intracellular carbon metabolism and the expression of virulence genes.
新技术,如高通量方法和 13C-同位素特征分析,开始为我们提供对微生物体内代谢的深入了解,特别是在被细胞内细菌病原体定殖的宿主细胞隔室中。在这篇综述中,我们讨论了确定在感染宿主细胞的细胞质或空泡中复制的模式细胞内细菌病原体所使用的主要碳源和代谢途径的最新进展。此外,我们强调了细胞内碳代谢与毒力基因表达之间的可能联系。