Griffiths E J, Kretschmer M, Kronstad J W
The Michael Smith Laboratories, Department of Microbiology and Immunology, and Faculty of Land and Food Systems, University of British Columbia, Vancouver, B.C., V6T 1Z4, Canada.
Fungal Biol Rev. 2012 Oct 1;26(2-3):61-72. doi: 10.1016/j.fbr.2012.02.004. Epub 2012 Mar 30.
The pathogenic fungus Cryptococcus neoformans exhibits a striking propensity to cause central nervous system (CNS) disease in people with HIV/AIDS. Given that cryptococcal infections are generally initiated by pulmonary colonization, dissemination requires that the fungus withstand phagocytic killing, cross the alveolar-capillary interface in the lung, survive in the circulatory system and breach the blood-brain barrier. We know little about the molecular mechanisms underlying dissemination, but there is a rapidly growing list of mutants that fail to cause CNS disease. These mutants reveal a remarkable diversity of functions and therefore illustrate the complexity of the cryptococcal-host interaction. The challenge now is to extend the analysis of these mutants to acquire a detailed understanding of each step in dissemination.
致病性真菌新型隐球菌在感染艾滋病毒/艾滋病的人群中极有可能引发中枢神经系统(CNS)疾病。鉴于隐球菌感染通常始于肺部定植,其传播需要该真菌抵御吞噬细胞的杀伤,穿过肺部的肺泡-毛细血管界面,在循环系统中存活并突破血脑屏障。我们对其传播背后的分子机制知之甚少,但未能引发中枢神经系统疾病的突变体数量正在迅速增加。这些突变体显示出功能的显著多样性,因此说明了隐球菌与宿主相互作用的复杂性。目前的挑战是扩大对这些突变体的分析,以详细了解传播过程中的每一个步骤。