Price Michael S, Nichols Connie B, Alspaugh J Andrew
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Infect Immun. 2008 Dec;76(12):5729-37. doi: 10.1128/IAI.00896-08. Epub 2008 Sep 8.
Rho-GDP dissociation inhibitors (Rho-GDI) are repressors of Rho-type monomeric GTPases that control fundamental cellular processes, such as cytoskeletal arrangement, vesicle trafficking, and polarized growth. We identified and altered the expression of the gene encoding a Rho-GDI homolog in the human fungal pathogen Cryptococcus neoformans and investigated its impact on pathogenicity in animal models of cryptococcosis. Consistent with its predicted function to inhibit and sequester Rho-type GTPases, overexpression of RDI1 results in cytosolic localization of Cdc42. Likely as a result of this finding, RDI1-overexpressing strains exhibited altered morphology compared to that of the wild type, with apparent defects in maintaining proper cell polarity and cytokinesis. RDI1 deletion resulted in increased vacuole size in tissue culture medium and aberrant cell morphology at neutral pH. Maintenance of normal cell morphology is vital for C. neoformans pathogenicity. Accordingly, the rdi1Delta mutant strain also showed reduced intracellular survival in macrophages and severe attenuation of virulence in two murine models of cryptococcosis. This reduction in virulence of the rdi1Delta mutant occurs in the absence of major growth defects in rich medium and with classical virulence-associated phenotypes.
Rho-GDP解离抑制剂(Rho-GDI)是Rho型单体GTP酶的抑制因子,这些GTP酶控制着诸如细胞骨架排列、囊泡运输和极性生长等基本细胞过程。我们在人类真菌病原体新型隐球菌中鉴定并改变了编码Rho-GDI同源物的基因的表达,并在隐球菌病动物模型中研究了其对致病性的影响。与其抑制和隔离Rho型GTP酶的预测功能一致,RDI1的过表达导致Cdc42定位于细胞质中。可能是由于这一发现,与野生型相比,过表达RDI1的菌株表现出形态改变,在维持适当的细胞极性和胞质分裂方面存在明显缺陷。RDI1缺失导致组织培养基中液泡大小增加,在中性pH值下细胞形态异常。维持正常细胞形态对新型隐球菌的致病性至关重要。因此,rdi1Delta突变菌株在巨噬细胞中的细胞内存活率也降低,并且在两种隐球菌病小鼠模型中毒力严重减弱。rdi1Delta突变体毒力的降低发生在丰富培养基中没有主要生长缺陷且具有经典毒力相关表型的情况下。