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在efg1突变体中,白色念珠菌菌丝非依赖性蛋白酶基因SAP1和SAP3的表达降低,这与感染口腔上皮期间毒力减弱有关。

Reduced expression of the hyphal-independent Candida albicans proteinase genes SAP1 and SAP3 in the efg1 mutant is associated with attenuated virulence during infection of oral epithelium.

作者信息

Korting Hans C, Hube Bernhard, Oberbauer Sylvia, Januschke Elfriede, Hamm Gerald, Albrecht Antje, Borelli Claudia, Schaller Martin

机构信息

Department of Dermatology and Allergology1 and Department of Parodontology3, University of Munich, Munich, Germany 2Robert Koch-Institut, Berlin, Germany.

出版信息

J Med Microbiol. 2003 Aug;52(Pt 8):623-632. doi: 10.1099/jmm.0.05125-0.

Abstract

The transition of Candida albicans from a yeast to a hyphal form is controlled by several transcriptional factors, including the key regulators Cph1 and Efg1, and is considered an important virulence attribute. These factors, especially Efg1, regulate the expression of hyphal-associated genes e.g. SAP4-SAP6. In order to investigate the relevance of these transcriptional regulators for hyphal-independent SAP genes, recently constructed cph1 and efg1 single mutants and a cph1/efg1 double mutant lacking these factors were tested during interaction with oral epithelium and polymorphonuclear neutrophils. In contrast to the parental wild-type strain and the cph1 mutant, the efg1 and the cph1/efg1 mutants did not produce hyphal forms in all experiments and were less capable of damaging epithelial cells and neutrophil granulocytes. The attenuated epithelial lesions of these mutants were correlated not only with reduced expression of the hyphal-associated gene SAP4, but also with the lack of SAP1 and SAP3 expression previously shown to be important for oral infections. An efg1 mutant strain carrying a plasmid-borne copy of the EFG1 gene regained hyphal growth, damage of keratinocytes, granulocytes and the expression of SAP1 and SAP3. Although efg1 and cph1/efg1 mutants did not produce germ tubes during infection, expression of the hyphal-associated genes SAP5 and SAP6 was not completely abolished. A reduced capacity to stimulate an epithelial immune response manifested by a delayed onset of IL-1beta, IL-8 and TNF expression was only observed in the cph1/efg1-infected tissue. These results provide further evidence for a combined regulation of different virulence factors, such as dimorphism and expression of SAP genes. Furthermore, it could be demonstrated that the lack of Efg1 also caused reduced expression of hyphal-independent SAP genes. Both the EFG1 and the CPH1 gene products are necessary for adequate induction of an immune response.

摘要

白色念珠菌从酵母形态向菌丝形态的转变受多种转录因子调控,包括关键调节因子Cph1和Efg1,这一转变被认为是一种重要的毒力属性。这些因子,尤其是Efg1,调控与菌丝相关基因(如SAP4 - SAP6)的表达。为了研究这些转录调节因子与不依赖菌丝的SAP基因的相关性,最近构建的cph1和efg1单突变体以及缺乏这些因子的cph1/efg1双突变体在与口腔上皮细胞和多形核中性粒细胞相互作用的过程中接受了检测。与亲本野生型菌株和cph1突变体不同,efg1和cph1/efg1突变体在所有实验中均未形成菌丝形态,且损伤上皮细胞和中性粒细胞的能力较弱。这些突变体导致的上皮损伤减轻不仅与菌丝相关基因SAP4表达降低有关,还与先前显示对口腔感染很重要的SAP1和SAP3表达缺失有关。携带质粒介导的EFG1基因拷贝的efg1突变菌株恢复了菌丝生长、对角质形成细胞和粒细胞的损伤以及SAP1和SAP3的表达。尽管efg1和cph1/efg1突变体在感染过程中未产生芽管,但与菌丝相关的基因SAP5和SAP6的表达并未完全消除。仅在cph1/efg1感染的组织中观察到刺激上皮免疫反应的能力降低,表现为IL - 1β、IL - 8和TNF表达延迟。这些结果为不同毒力因子(如双态性和SAP基因表达)的联合调控提供了进一步证据。此外,还可以证明Efg1的缺失也导致不依赖菌丝的SAP基因表达降低。EFG1和CPH1基因产物对于充分诱导免疫反应都是必需的。

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