Department of Immunology and Infectious Diseases, Harvard School of Public Health, 665 Huntington Avenue, Building I, Room 817, Boston, MA 02115, USA.
Cell Host Microbe. 2013 Jan 16;13(1):108-17. doi: 10.1016/j.chom.2012.11.011.
Metabolic coupling of intracellular pathogens with host cells is essential for successful colonization of the host. Establishment of intracellular infection by the protozoan Trypanosoma cruzi leads to the development of human Chagas' disease, yet the functional contributions of the host cell toward the infection process remain poorly characterized. Here, a genome-scale functional screen identified interconnected metabolic networks centered around host energy production, nucleotide metabolism, pteridine biosynthesis, and fatty acid oxidation as key processes that fuel intracellular T. cruzi growth. Additionally, the host kinase Akt, which plays essential roles in various cellular processes, was critical for parasite replication. Targeted perturbations in these host metabolic pathways or Akt-dependent signaling pathways modulated the parasite's replicative capacity, highlighting the adaptability of this intracellular pathogen to changing conditions in the host. These findings identify key cellular process regulating intracellular T. cruzi growth and illuminate the potential to leverage host pathways to limit T. cruzi infection.
细胞内病原体与宿主细胞的代谢偶联对于成功定殖宿主至关重要。原生动物克氏锥虫的细胞内感染的建立导致人类恰加斯病的发生,但宿主细胞对感染过程的功能贡献仍知之甚少。在这里,一项基于基因组规模的功能筛选确定了以宿主能量产生、核苷酸代谢、蝶呤生物合成和脂肪酸氧化为中心的相互关联的代谢网络,这些都是为细胞内克氏锥虫生长提供燃料的关键过程。此外,在各种细胞过程中发挥重要作用的宿主激酶 Akt 对于寄生虫的复制也是至关重要的。这些宿主代谢途径或 Akt 依赖性信号途径的靶向扰动调节了寄生虫的复制能力,突出了这种细胞内病原体对宿主内环境变化的适应性。这些发现确定了调节细胞内克氏锥虫生长的关键细胞过程,并阐明了利用宿主途径来限制克氏锥虫感染的潜力。