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内吞成分VPS28和VPS32的缺失通过白色念珠菌中依赖RIM101和不依赖RIM101的途径影响碱性pH条件下的生长及毒力。

Deletions of endocytic components VPS28 and VPS32 affect growth at alkaline pH and virulence through both RIM101-dependent and RIM101-independent pathways in Candida albicans.

作者信息

Cornet Muriel, Bidard Frédérique, Schwarz Patrick, Da Costa Grégory, Blanchin-Roland Sylvie, Dromer Françoise, Gaillardin Claude

机构信息

Laboratoire de Microbiologie et Génétique Moléculaire, INRA, CBAI, 78850 Thiverval-Grignon, France.

出版信息

Infect Immun. 2005 Dec;73(12):7977-87. doi: 10.1128/IAI.73.12.7977-7987.2005.

Abstract

Ambient pH signaling involves a cascade of conserved Rim or Pal products in ascomycetous yeasts or filamentous fungi, respectively. Recent evidences in the fungi Aspergillus nidulans, Saccharomyces cerevisiae, Yarrowia lipolytica, and Candida albicans suggested that components of endosomal sorting complexes required for transport (ESCRT) involved in endocytic trafficking were needed for signal transduction along the Rim pathway. In this study, we confirm these findings with C. albicans and show that Vps28p (ESCRT-I) and Vps32p/Snf7p (ESCRT-III) are required for the transcriptional regulation of known targets of the Rim pathway, such as the PHR1 and PHR2 genes encoding cell surface proteins, which are expressed at alkaline and acidic pH, respectively. We additionally show that deletion of these two VPS genes, particularly VPS32, has a more drastic effect than a RIM101 deletion on growth at alkaline pH and that this effect is only partially suppressed by expression of a constitutively active form of Rim101p. Finally, in an in vivo mouse model, both vps null mutants were significantly less virulent than a rim101 mutant, suggesting that VPS28 and VPS32 gene products affect virulence both through Rim-dependent and Rim-independent pathways.

摘要

环境pH信号传导分别涉及子囊菌酵母或丝状真菌中一系列保守的Rim或Pal产物。最近在构巢曲霉、酿酒酵母、解脂耶氏酵母和白色念珠菌中的证据表明,参与内吞运输的内体分选复合物(ESCRT)的组分是沿Rim途径进行信号转导所必需的。在本研究中,我们用白色念珠菌证实了这些发现,并表明Vps28p(ESCRT-I)和Vps32p/Snf7p(ESCRT-III)是Rim途径已知靶标的转录调控所必需的,例如分别在碱性和酸性pH下表达的编码细胞表面蛋白的PHR1和PHR2基因。我们还表明,这两个VPS基因的缺失,特别是VPS32的缺失,在碱性pH下对生长的影响比RIM101缺失更显著,并且这种影响仅被组成型活性形式的Rim101p的表达部分抑制。最后,在体内小鼠模型中,两个vps缺失突变体的毒力均显著低于rim101突变体,这表明VPS28和VPS32基因产物通过Rim依赖性和Rim非依赖性途径影响毒力。

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