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Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells

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 ch...

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Autores principales: Almeida, Fausto, Antoniêto, Amanda Cristina Campos, Pessoni, André Moreira, Monteiro, Valdirene Neves, Alegre-Maller, Ana Claudia Paiva, Pigosso, Laurine Lacerda, Pereira, Maristela, Soares, Célia Maria de Almeida, Roque-Barreira, Maria Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864839/
https://www.ncbi.nlm.nih.gov/pubmed/27226767
http://dx.doi.org/10.2174/1389202917666151116212705
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author Almeida, Fausto
Antoniêto, Amanda Cristina Campos
Pessoni, André Moreira
Monteiro, Valdirene Neves
Alegre-Maller, Ana Claudia Paiva
Pigosso, Laurine Lacerda
Pereira, Maristela
Soares, Célia Maria de Almeida
Roque-Barreira, Maria Cristina
author_facet Almeida, Fausto
Antoniêto, Amanda Cristina Campos
Pessoni, André Moreira
Monteiro, Valdirene Neves
Alegre-Maller, Ana Claudia Paiva
Pigosso, Laurine Lacerda
Pereira, Maristela
Soares, Célia Maria de Almeida
Roque-Barreira, Maria Cristina
author_sort Almeida, Fausto
collection PubMed
description 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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spelling pubmed-48648392016-10-01 Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells Almeida, Fausto Antoniêto, Amanda Cristina Campos Pessoni, André Moreira Monteiro, Valdirene Neves Alegre-Maller, Ana Claudia Paiva Pigosso, Laurine Lacerda Pereira, Maristela Soares, Célia Maria de Almeida Roque-Barreira, Maria Cristina Curr Genomics Article 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. Bentham Science Publishers 2016-04 2016-04 /pmc/articles/PMC4864839/ /pubmed/27226767 http://dx.doi.org/10.2174/1389202917666151116212705 Text en © 2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Almeida, Fausto
Antoniêto, Amanda Cristina Campos
Pessoni, André Moreira
Monteiro, Valdirene Neves
Alegre-Maller, Ana Claudia Paiva
Pigosso, Laurine Lacerda
Pereira, Maristela
Soares, Célia Maria de Almeida
Roque-Barreira, Maria Cristina
Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells
title Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells
title_full Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells
title_fullStr Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells
title_full_unstemmed Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells
title_short Influence of N-glycans on Expression of Cell Wall Remodeling Related Genes in Paracoccidioides brasiliensis Yeast Cells
title_sort influence of n-glycans on expression of cell wall remodeling related genes in paracoccidioides brasiliensis yeast cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864839/
https://www.ncbi.nlm.nih.gov/pubmed/27226767
http://dx.doi.org/10.2174/1389202917666151116212705
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