Cargando…

Novel Entries in a Fungal Biofilm Matrix Encyclopedia

Virulence of Candida is linked with its ability to form biofilms. Once established, biofilm infections are nearly impossible to eradicate. Biofilm cells live immersed in a self-produced matrix, a blend of extracellular biopolymers, many of which are uncharacterized. In this study, we provide a compr...

Descripción completa

Detalles Bibliográficos
Autores principales: Zarnowski, Robert, Westler, William M., Lacmbouh, Ghislain Ade, Marita, Jane M., Bothe, Jameson R., Bernhardt, Jörg, Lounes-Hadj Sahraoui, Anissa, Fontaine, Joël, Sanchez, Hiram, Hatfield, Ronald D., Ntambi, James M., Nett, Jeniel E., Mitchell, Aaron P., Andes, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128356/
https://www.ncbi.nlm.nih.gov/pubmed/25096878
http://dx.doi.org/10.1128/mBio.01333-14
_version_ 1782330118079774720
author Zarnowski, Robert
Westler, William M.
Lacmbouh, Ghislain Ade
Marita, Jane M.
Bothe, Jameson R.
Bernhardt, Jörg
Lounes-Hadj Sahraoui, Anissa
Fontaine, Joël
Sanchez, Hiram
Hatfield, Ronald D.
Ntambi, James M.
Nett, Jeniel E.
Mitchell, Aaron P.
Andes, David R.
author_facet Zarnowski, Robert
Westler, William M.
Lacmbouh, Ghislain Ade
Marita, Jane M.
Bothe, Jameson R.
Bernhardt, Jörg
Lounes-Hadj Sahraoui, Anissa
Fontaine, Joël
Sanchez, Hiram
Hatfield, Ronald D.
Ntambi, James M.
Nett, Jeniel E.
Mitchell, Aaron P.
Andes, David R.
author_sort Zarnowski, Robert
collection PubMed
description Virulence of Candida is linked with its ability to form biofilms. Once established, biofilm infections are nearly impossible to eradicate. Biofilm cells live immersed in a self-produced matrix, a blend of extracellular biopolymers, many of which are uncharacterized. In this study, we provide a comprehensive analysis of the matrix manufactured by Candida albicans both in vitro and in a clinical niche animal model. We further explore the function of matrix components, including the impact on drug resistance. We uncovered components from each of the macromolecular classes (55% protein, 25% carbohydrate, 15% lipid, and 5% nucleic acid) in the C. albicans biofilm matrix. Three individual polysaccharides were identified and were suggested to interact physically. Surprisingly, a previously identified polysaccharide of functional importance, β-1,3-glucan, comprised only a small portion of the total matrix carbohydrate. Newly described, more abundant polysaccharides included α-1,2 branched α-1,6-mannans (87%) associated with unbranched β-1,6-glucans (13%) in an apparent mannan-glucan complex (MGCx). Functional matrix proteomic analysis revealed 458 distinct activities. The matrix lipids consisted of neutral glycerolipids (89.1%), polar glycerolipids (10.4%), and sphingolipids (0.5%). Examination of matrix nucleic acid identified DNA, primarily noncoding sequences. Several of the in vitro matrix components, including proteins and each of the polysaccharides, were also present in the matrix of a clinically relevant in vivo biofilm. Nuclear magnetic resonance (NMR) analysis demonstrated interaction of aggregate matrix with the antifungal fluconazole, consistent with a role in drug impedance and contribution of multiple matrix components.
format Online
Article
Text
id pubmed-4128356
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher American Society of Microbiology
record_format MEDLINE/PubMed
spelling pubmed-41283562014-08-12 Novel Entries in a Fungal Biofilm Matrix Encyclopedia Zarnowski, Robert Westler, William M. Lacmbouh, Ghislain Ade Marita, Jane M. Bothe, Jameson R. Bernhardt, Jörg Lounes-Hadj Sahraoui, Anissa Fontaine, Joël Sanchez, Hiram Hatfield, Ronald D. Ntambi, James M. Nett, Jeniel E. Mitchell, Aaron P. Andes, David R. mBio Research Article Virulence of Candida is linked with its ability to form biofilms. Once established, biofilm infections are nearly impossible to eradicate. Biofilm cells live immersed in a self-produced matrix, a blend of extracellular biopolymers, many of which are uncharacterized. In this study, we provide a comprehensive analysis of the matrix manufactured by Candida albicans both in vitro and in a clinical niche animal model. We further explore the function of matrix components, including the impact on drug resistance. We uncovered components from each of the macromolecular classes (55% protein, 25% carbohydrate, 15% lipid, and 5% nucleic acid) in the C. albicans biofilm matrix. Three individual polysaccharides were identified and were suggested to interact physically. Surprisingly, a previously identified polysaccharide of functional importance, β-1,3-glucan, comprised only a small portion of the total matrix carbohydrate. Newly described, more abundant polysaccharides included α-1,2 branched α-1,6-mannans (87%) associated with unbranched β-1,6-glucans (13%) in an apparent mannan-glucan complex (MGCx). Functional matrix proteomic analysis revealed 458 distinct activities. The matrix lipids consisted of neutral glycerolipids (89.1%), polar glycerolipids (10.4%), and sphingolipids (0.5%). Examination of matrix nucleic acid identified DNA, primarily noncoding sequences. Several of the in vitro matrix components, including proteins and each of the polysaccharides, were also present in the matrix of a clinically relevant in vivo biofilm. Nuclear magnetic resonance (NMR) analysis demonstrated interaction of aggregate matrix with the antifungal fluconazole, consistent with a role in drug impedance and contribution of multiple matrix components. American Society of Microbiology 2014-08-05 /pmc/articles/PMC4128356/ /pubmed/25096878 http://dx.doi.org/10.1128/mBio.01333-14 Text en Copyright © 2014 Zarnowski et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zarnowski, Robert
Westler, William M.
Lacmbouh, Ghislain Ade
Marita, Jane M.
Bothe, Jameson R.
Bernhardt, Jörg
Lounes-Hadj Sahraoui, Anissa
Fontaine, Joël
Sanchez, Hiram
Hatfield, Ronald D.
Ntambi, James M.
Nett, Jeniel E.
Mitchell, Aaron P.
Andes, David R.
Novel Entries in a Fungal Biofilm Matrix Encyclopedia
title Novel Entries in a Fungal Biofilm Matrix Encyclopedia
title_full Novel Entries in a Fungal Biofilm Matrix Encyclopedia
title_fullStr Novel Entries in a Fungal Biofilm Matrix Encyclopedia
title_full_unstemmed Novel Entries in a Fungal Biofilm Matrix Encyclopedia
title_short Novel Entries in a Fungal Biofilm Matrix Encyclopedia
title_sort novel entries in a fungal biofilm matrix encyclopedia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128356/
https://www.ncbi.nlm.nih.gov/pubmed/25096878
http://dx.doi.org/10.1128/mBio.01333-14
work_keys_str_mv AT zarnowskirobert novelentriesinafungalbiofilmmatrixencyclopedia
AT westlerwilliamm novelentriesinafungalbiofilmmatrixencyclopedia
AT lacmbouhghislainade novelentriesinafungalbiofilmmatrixencyclopedia
AT maritajanem novelentriesinafungalbiofilmmatrixencyclopedia
AT bothejamesonr novelentriesinafungalbiofilmmatrixencyclopedia
AT bernhardtjorg novelentriesinafungalbiofilmmatrixencyclopedia
AT louneshadjsahraouianissa novelentriesinafungalbiofilmmatrixencyclopedia
AT fontainejoel novelentriesinafungalbiofilmmatrixencyclopedia
AT sanchezhiram novelentriesinafungalbiofilmmatrixencyclopedia
AT hatfieldronaldd novelentriesinafungalbiofilmmatrixencyclopedia
AT ntambijamesm novelentriesinafungalbiofilmmatrixencyclopedia
AT nettjeniele novelentriesinafungalbiofilmmatrixencyclopedia
AT mitchellaaronp novelentriesinafungalbiofilmmatrixencyclopedia
AT andesdavidr novelentriesinafungalbiofilmmatrixencyclopedia