巴西副球虫病
副球虫病
衣霉素
细胞壁
糖蛋白
糖基化
生物
聚糖
基因
基因表达
二型真菌
微生物学
副球虫病
葡聚糖
酵母
生物化学
未折叠蛋白反应
作者
Fausto Almeida,Amanda Antoniêto,André Moreira Pessoni,Valdirene Neves Monteiro,Ana Cláudia Paiva Alegre-Maller,Laurine Lacerda Pigosso,Maristela Pereira,Célia Maria de Almeida Soares,Maria Cristina Roque‐Barreira
出处
期刊:Current Genomics
[Bentham Science Publishers]
日期:2015-11-30
卷期号:17 (2): 112-118
被引量:12
标识
DOI:10.2174/1389202917666151116212705
摘要
Paracoccidioidomycosis is the most prevalent systemic mycosis in Latin America. It is caused by the temperature-dependent dimorphic fungus Paracoccidioides brasiliensis. The P. brasiliensis cell wall is a dynamic outer structure, composed of a network of glycoproteins and polysaccharides, such as chitin, glucan and N-glycosylated proteins. These glycoproteins can interact with the host to affect infection rates, and are known to perform other functions. We inhibited N-linked glycosylation using tunicamycin (TM), and then evaluated the expression of P. brasiliensis genes related to cell wall remodeling. Our results suggest that cell wall synthesis related genes, such as β-1,3-glucanosyltransferase (PbGEL3), 1,3-β-D-glucan synthase (PbFKS1), and α-1,4-amylase (PbAMY), as well as cell wall degrading related genes, such as N-acetyl-β-D-glucosaminidase (PbNAG1), α-1,3-glucanase (PbAGN), and β-1,3-glucanase (PbBGN1 and PbBGN2), have their expression increased by the N-glycosylation inhibition, as detected by qRT-PCR. The observed increases in gene expression levels reveal possible compensatory mechanisms for diminished enzyme activity due to the lack of glycosylation caused by TM.
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