Department of Molecular and Cellular Biology, Harvard University, Boston, MA, USA.
Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Nat Rev Microbiol. 2020 Jan;18(1):47-59. doi: 10.1038/s41579-019-0273-7. Epub 2019 Nov 14.
Mycobacterium tuberculosis, the leading cause of death due to infection, has a dynamic and immunomodulatory cell envelope. The cell envelope structurally and functionally varies across the length of the cell and during the infection process. This variability allows the bacterium to manipulate the human immune system, tolerate antibiotic treatment and adapt to the variable host environment. Much of what we know about the mycobacterial cell envelope has been gleaned from model actinobacterial species, or model conditions such as growth in vitro, in macrophages and in the mouse. In this Review, we combine data from different experimental systems to build a model of the dynamics of the mycobacterial cell envelope across space and time. We describe the regulatory pathways that control metabolism of the cell wall and surface lipids in M. tuberculosis during growth and stasis, and speculate about how this regulation might affect antibiotic susceptibility and interactions with the immune system.
结核分枝杆菌是感染导致死亡的主要原因,它具有动态和免疫调节的细胞包膜。细胞包膜在细胞长度和感染过程中在结构和功能上都有所不同。这种可变性使细菌能够操纵人体免疫系统、耐受抗生素治疗并适应宿主环境的变化。我们对分枝杆菌细胞包膜的了解主要来自于模式放线菌物种,或体外培养、巨噬细胞内和小鼠体内等模型条件。在这篇综述中,我们结合来自不同实验系统的数据,构建了分枝杆菌细胞包膜在空间和时间上的动态模型。我们描述了控制结核分枝杆菌在生长和静止期细胞壁和表面脂质代谢的调控途径,并推测这种调控可能如何影响抗生素敏感性和与免疫系统的相互作用。