首页> 外文期刊>Virulence. >Identification and characterization of ORF19.1725 , a novel gene contributing to the white cell pheromone response and virulence-associated functions in Candida albicans
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Identification and characterization of ORF19.1725 , a novel gene contributing to the white cell pheromone response and virulence-associated functions in Candida albicans

机译:鉴定和表征ORF19.1725,一个新基因,在白色念珠菌中有助于白细胞信息素应答和毒力相关功能

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ABSTRACT An epigenetic transition between white cells and opaque cells influences several properties of Candida albicans biology, including cellular morphology, biofilm formation, virulence, and sexual mating. In particular, these two cell types exhibit marked differences in their ability to undergo sex. A previous study identified the transcriptional regulator of pheromone response in both the white and opaque states as Cph1 because deletion of this gene abolished both pheromone-induced cell adhesion in white cells and sexual mating in opaque cells. To further explore how these cell types exhibit distinct biological outputs upon pheromone stimulation, we selected five Cph1-regulated genes with significant expression during the pheromone response in the white state but not the opaque state. These phase-specific pheromone-induced genes are ORF19.1539, ORF19.1725, ORF19.2430, ORF19.2691 and ORF19.5557. Deletion of each gene revealed that orf19.1539Δ, orf19.1725Δ, orf19.2430Δ and orf19.5557Δ showed significant decreases in pheromone-stimulated cell adhesion in the white state but retained normal mating competency in the opaque state, indicating that a particular role in white cell pheromone response is mediated by these four genes. Interestingly, the defects of orf19.1725Δ in pheromone-stimulated cell adhesion also abolished conventional biofilms and hyphal growth. Zebrafish egg infection assays further demonstrated that ORF19.1725 is involved in cell adhesion, penetration and virulence. Overall, four Cph1-regulated downstream targets were identified in the regulation of white cell pheromone response. We also clarified the roles of C. albicans ORF19.1725 in cell adhesion, hyphal growth, biofilm formation and virulence.
机译:摘要白细胞和不透明细胞之间的表观遗传转变影响白色念珠菌的生物学特性,包括细胞形态,生物膜形成,毒力和性交。特别地,这两种细胞类型表现出明显的性能力差异。先前的研究将白色和不透明状态下信息素应答的转录调节因子都识别为Cph1,因为该基因的缺失消除了白细胞中信息素诱导的细胞粘附以及不透明细胞中的性交。为了进一步探索这些细胞类型在信息素刺激下如何表现出独特的生物学输出,我们选择了五个由Cph1调控的基因,这些信息素在白色状态下(而不是不透明状态)的信息素反应期间具有明显的表达。这些相特异性信息素诱导的基因是ORF19.1539,ORF19.1725,ORF19.2430,ORF19.2691和ORF19.5557。每个基因的缺失显示,orf19.1539Δ,orf19.1725Δ,orf19.2430Δ和orf19.5557Δ在白色状态下显示了由信息素刺激的细胞粘附的显着降低,但在不透明状态下保留了正常的交配能力,表明在这四个基因介导白细胞信息素反应。有趣的是,信息素刺激的细胞粘附中orf19.1725Δ的缺陷也消除了常规生物膜和菌丝的生长。斑马鱼卵感染试验进一步证明,ORF19.1725与细胞粘附,渗透和毒力有关。总体而言,在白细胞信息素反应的调控中,确定了四个受Cph1调控的下游靶标。我们还阐明了白色念珠菌ORF19.1725在细胞粘附,菌丝生长,生物膜形成和毒力中的作用。

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