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磷脂酶D1在白色念珠菌生长和二态性过程中的作用及相关性

The role and relevance of phospholipase D1 during growth and dimorphism of Candida albicans.

作者信息

Hube Bernhard, Hess Daniela, Baker Carol A, Schaller Martin, Schäfer Wilhelm, Dolan Joseph W

机构信息

Robert Koch-Institut, NG4, Nordufer 20, D-13353 Berlin, Germany3.

Institut für Allgemeine Botanik, AMP III, Universität Hamburg, Ohnhorststr. 18, D-22609 Hamburg, Germany1.

出版信息

Microbiology (Reading). 2001 Apr;147(Pt 4):879-889. doi: 10.1099/00221287-147-4-879.

Abstract

The phosphatidylcholine-specific phospholipase D1 (PLD1) in Saccharomyces cerevisiae is involved in vesicle transport and is essential for sporulation. The gene encoding the homologous phospholipase D1 from Candida albicans (PLD1) was used to study the role of PLD1 in this pathogenic fungus. In vitro and in vivo expression studies using Northern blots and reverse transcriptase-PCR showed low PLD1 mRNA levels in defined media supporting yeast growth and during experimental infection, while enhanced levels of PLD1 transcripts were detected during the yeast to hyphal transition. To study the relevance of PLD1 during yeast and hyphal growth, an essential part of the gene was deleted in both alleles of two isogenic strains. In vitro PLD1 activity assays showed that pld1 mutants produced no detectable levels of phosphatidic acid, the hydrolytic product of PLD1 activity, and strongly reduced levels of diacylglycerol, the product of lipid phosphate phosphohydrolase, suggesting no or a negligible background PLD1 activity in the pld1 mutants. The pld1 mutants showed no growth differences compared to the parental wild-type in liquid complex and minimal media, independent of the growth temperature. In addition, growth rates of pld1 mutants in media with protein as the sole source of nitrogen were similar to growth rates of the wild-type, indicating that secretion of proteinases was not reduced. Chlamydospore formation was normal in pld1 mutants. When germ tube formation was induced in liquid media, pld1 mutants showed similar rates of yeast to hyphal transition compared to the wild-type. However, no hyphae formation was observed on solid Spider medium, and cell growth on cornmeal/Tween 80 medium indicated aberrant morphogenesis. In addition, pld1 mutants growing on solid media had an attenuated ability to invade the agar. In a model of oral candidosis, pld1 mutants showed no attenuation of virulence. In contrast, the mutant was less virulent in two different mouse models. These data suggest that PLD1 is not essential for growth and oral infections. However, they also suggest that a prominent part of the phosphatidic acid and diacylglycerol pools is produced by PLD1 and that the level of these components is important for morphological transitions under certain conditions in C. albicans.

摘要

酿酒酵母中的磷脂酰胆碱特异性磷脂酶D1(PLD1)参与囊泡运输,对孢子形成至关重要。利用白色念珠菌同源磷脂酶D1(PLD1)的编码基因来研究PLD1在这种致病真菌中的作用。使用Northern印迹和逆转录聚合酶链反应进行的体外和体内表达研究表明,在支持酵母生长的特定培养基中以及实验感染期间,PLD1 mRNA水平较低,而在酵母向菌丝转变过程中检测到PLD1转录本水平升高。为了研究PLD1在酵母和菌丝生长过程中的相关性,在两个同基因菌株的两个等位基因中都删除了该基因的一个重要部分。体外PLD1活性测定表明,pld1突变体产生的磷脂酸(PLD1活性的水解产物)水平无法检测到,脂质磷酸磷酸水解酶的产物二酰甘油水平也大幅降低,这表明pld1突变体中不存在或背景PLD1活性可忽略不计。与亲本野生型相比,pld1突变体在液体复合培养基和基本培养基中的生长没有差异,与生长温度无关。此外,pld1突变体在以蛋白质作为唯一氮源的培养基中的生长速率与野生型相似,这表明蛋白酶的分泌没有减少。pld1突变体中的厚垣孢子形成正常。当在液体培养基中诱导芽管形成时,与野生型相比,pld1突变体显示出相似的酵母向菌丝转变速率。然而,在固体蜘蛛培养基上未观察到菌丝形成,在玉米粉/吐温80培养基上的细胞生长表明形态发生异常。此外,在固体培养基上生长的pld1突变体侵入琼脂的能力减弱。在口腔念珠菌病模型中,pld1突变体的毒力没有减弱。相比之下,该突变体在两种不同的小鼠模型中毒力较低。这些数据表明,PLD1对生长和口腔感染并非必不可少。然而,它们也表明磷脂酸和二酰甘油库的很大一部分是由PLD1产生的,并且这些成分的水平在白色念珠菌的某些条件下对形态转变很重要。

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