RFG1 Regulation of Candida albicans Filamentation and Virulence

描述（由申请方提供）：白色念珠菌是迄今为止最常见的人体分离真菌。它是人类的正常器官，但也能够侵入身体的几乎每个部位并引起感染，特别是在不断扩大的免疫功能低下的宿主群体中，包括感染艾滋病毒的宿主。该生物体能够在单细胞酵母样形式（芽生孢子）和丝状形式（根据丝状结构的轻微变化称为菌丝或假菌丝）之间进行可逆的形态转变，以响应外部环境的变化，这种能力被认为是其致病潜力的关键。然而，这种信念主要是基于从大量的毒力研究中获得的结果，使用C。不能经历这种形态发生转换的白念珠菌突变株（即，δ-cph 1、δ-efg 1、δ-tup 1、δ-nrg 1）：因为所有这些菌株都以一种或另一种形式被锁定，所以不能对形态发生转换在毒力中的作用作出明确的结论。在以前的研究中，我们设计了一个条件突变株，其中一个负调控因子（NRG 1）的表达被置于四环素调控启动子的控制下。对该菌株的分析表明，这些形态学转变可以在体外和感染期间在动物（小鼠）宿主内进行修饰。在本申请中，我们建议将这些研究扩展到C.白色念珠菌（RFG 1），以更密切地检查和进一步确定这种重要的真菌病原体的感染过程。这将首先通过构建tet-RFG 1可调控的C来实现。白念珠菌菌株，因为我们做了NRG 1基因，然后分析其行为都在体外，然后在感染过程中。此外，我们将进行全基因组转录谱分析，以确定哪些C。白色念珠菌基因受Rfg 1 p蛋白的负调控，以及这些基因如何影响毒力。与公共卫生的相关性：白色念珠菌是念珠菌病的主要病原体，是最常见的真菌感染，现在是美国医院感染的第四大原因，死亡率高，经济负担飙升。这项研究背后的主要思想是进一步研究由关键调控基因控制的致病性和毒力之间的关系，这可能成为开发治疗这些感染的新策略的基础。

DESCRIPTION (provided by applicant): Candida albicans is by far the most frequently isolated fungus from humans. It is a normal commensal of Man but is also capable of invading almost every site in the body and causing infections especially in an expanding population of immunocompromised hosts, including those infected with HIV. The organism is able to undergo reversible morphological transitions between unicellular yeast-like forms (blastospores) and filamentous forms (called hyphae or pseudohyphae depending on slight variations in the structure of the filament), in response to changes in the external environment, and this ability is considered pivotal to its pathogenic potential. However, this belief is based primarily upon the results obtained from a large number of virulence studies using C. albicans mutant strains unable to undergo this morphogenetic switch (i.e. delta-cph1, delta-efg1, delta-tup1, delta-nrg1): because all of these strains are locked in one or other form, definitive conclusions on the role of the morphogenetic conversion in virulence cannot be made. In a previous study, we engineered a conditional mutant strain in which a negative regulator (NRG1) of filamentation was placed under the control of a tetracycline regulatable promoter. Analysis of this strain revealed that these morphological transitions could be modified both in vitro and also within an animal (mouse) host during an infection. In this application, we propose to extend these studies to the only other known negative regulator of this process in C. albicans (RFG1) to more closely examine and further define the infectious process of this important fungal pathogen. This will be achieved first through the construction of a tet-RFG1 regulatable C. albicans strain, as we did for the NRG1 gene, then analyzing its behavior both in vitro and then during the course of an infection. In addition, we will perform genome wide transcriptional profiling to determine which C. albicans genes are negatively regulated by the Rfg1p protein and how these impact on virulence. Relevance to public health: Candida albicans is the main causative agent of candidiasis, the most frequent fungal infection and now the fourth leading cause of infections in US hospitals, with high mortality rates and soaring economic burden. The main idea behind this study is to further investigate the relationship between filamentation and virulence, as controlled by key regulatory genes, which may serve as the basis for the development of novel strategies for the treatment of these infections.