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2000
Volume 17, Issue 2
  • ISSN: 1389-2029
  • E-ISSN: 1875-5488

Abstract

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 Nacetyl- 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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/content/journals/cg/10.2174/1389202917666151116212705
2016-04-01
2025-06-25
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  • Article Type:
    Research Article
Keyword(s): Cell wall; Fungal cell; N-glycan; Paracoccidioides brasiliensis
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