Luberto C, Toffaletti D L, Wills E A, Tucker S C, Casadevall A, Perfect J R, Hannun Y A, Del Poeta M
Department of Biochemistry & Molecular Biology, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Genes Dev. 2001 Jan 15;15(2):201-12. doi: 10.1101/gad.856001.
Cryptococcus neoformans is a leading cause of life-threatening fungal infection in immunocompromised patients. Inositol-phosphoryl ceramide synthase 1 (Ipc1) is a fungus-specific enzyme, encoded by the essential IPC1 gene, that catalyzes the formation of complex sphingolipids and may also regulate the levels of phytoceramide and diacylglycerol. Here, we investigated the functions of this essential gene by modulating its expression in C. neoformans using a galactose-inducible promoter. Down-regulation of IPC1 significantly lowers the expression of certain virulence traits such as melanin pigmentation and, remarkably, impairs pathogenicity of C. neoformans in an established rabbit model. Interestingly, we found that IPC1 down-regulation significantly decreases the intracellular growth of C. neoformans in the J774.16 murine macrophage-like cells. Finally, we studied the effect of IPC1 expression under different stress conditions and found that down-regulation of IPC1 confers a defect on in vitro growth at low pH. Because this environment is similar to that in the phagolysosome of J774.16 macrophage-like cells, our findings indicate that down-regulation of IPC1 confers a growth defect in vivo through a pH-dependent mechanism. In conclusion, our study is the first to define a novel and crucial function of Ipc1 in fungal pathogenesis.
新型隐球菌是免疫功能低下患者危及生命的真菌感染的主要病因。肌醇磷酸神经酰胺合酶1(Ipc1)是一种真菌特异性酶,由必需的IPC1基因编码,催化复杂鞘脂的形成,还可能调节植物神经酰胺和二酰基甘油的水平。在此,我们通过使用半乳糖诱导型启动子调节其在新型隐球菌中的表达,研究了这个必需基因的功能。IPC1的下调显著降低了某些毒力特征的表达,如黑色素沉着,并且值得注意的是,在已建立的兔模型中损害了新型隐球菌的致病性。有趣的是,我们发现IPC1的下调显著降低了新型隐球菌在J774.16鼠巨噬细胞样细胞中的细胞内生长。最后,我们研究了不同应激条件下IPC1表达的影响,发现IPC1的下调在低pH值下赋予体外生长缺陷。由于这种环境类似于J774.16巨噬细胞样细胞的吞噬溶酶体中的环境,我们的研究结果表明,IPC1的下调通过pH依赖性机制在体内赋予生长缺陷。总之,我们的研究首次确定了Ipc1在真菌致病机制中的一种新的关键功能。