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The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps
Neutrophils release extracellular traps (NETs) in response to planktonic C. albicans. These complexes composed of DNA, histones, and proteins inhibit Candida growth and dissemination. Considering the resilience of Candida biofilms to host defenses, we examined the neutrophil response to C. albicans...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021349/ https://www.ncbi.nlm.nih.gov/pubmed/27622514 http://dx.doi.org/10.1371/journal.ppat.1005884 |
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author | Johnson, Chad J. Cabezas-Olcoz, Jonathan Kernien, John F. Wang, Steven X. Beebe, David J. Huttenlocher, Anna Ansari, Hamayail Nett, Jeniel E. |
author_facet | Johnson, Chad J. Cabezas-Olcoz, Jonathan Kernien, John F. Wang, Steven X. Beebe, David J. Huttenlocher, Anna Ansari, Hamayail Nett, Jeniel E. |
author_sort | Johnson, Chad J. |
collection | PubMed |
description | Neutrophils release extracellular traps (NETs) in response to planktonic C. albicans. These complexes composed of DNA, histones, and proteins inhibit Candida growth and dissemination. Considering the resilience of Candida biofilms to host defenses, we examined the neutrophil response to C. albicans during biofilm growth. In contrast to planktonic C. albicans, biofilms triggered negligible release of NETs. Time lapse imaging confirmed the impairment in NET release and revealed neutrophils adhering to hyphae and migrating on the biofilm. NET inhibition depended on an intact extracellular biofilm matrix as physical or genetic disruption of this component resulted in NET release. Biofilm inhibition of NETosis could not be overcome by protein kinase C activation via phorbol myristate acetate (PMA) and was associated with suppression of neutrophil reactive oxygen species (ROS) production. The degree of impaired NET release correlated with resistance to neutrophil attack. The clinical relevance of the role for extracellular matrix in diminishing NET production was corroborated in vivo using a rat catheter model. The C. albicans pmr1Δ/Δ, defective in production of matrix mannan, appeared to elicit a greater abundance of NETs by scanning electron microscopy imaging, which correlated with a decreased fungal burden. Together, these findings show that C. albicans biofilms impair neutrophil response through an inhibitory pathway induced by the extracellular matrix. |
format | Online Article Text |
id | pubmed-5021349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50213492016-09-27 The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps Johnson, Chad J. Cabezas-Olcoz, Jonathan Kernien, John F. Wang, Steven X. Beebe, David J. Huttenlocher, Anna Ansari, Hamayail Nett, Jeniel E. PLoS Pathog Research Article Neutrophils release extracellular traps (NETs) in response to planktonic C. albicans. These complexes composed of DNA, histones, and proteins inhibit Candida growth and dissemination. Considering the resilience of Candida biofilms to host defenses, we examined the neutrophil response to C. albicans during biofilm growth. In contrast to planktonic C. albicans, biofilms triggered negligible release of NETs. Time lapse imaging confirmed the impairment in NET release and revealed neutrophils adhering to hyphae and migrating on the biofilm. NET inhibition depended on an intact extracellular biofilm matrix as physical or genetic disruption of this component resulted in NET release. Biofilm inhibition of NETosis could not be overcome by protein kinase C activation via phorbol myristate acetate (PMA) and was associated with suppression of neutrophil reactive oxygen species (ROS) production. The degree of impaired NET release correlated with resistance to neutrophil attack. The clinical relevance of the role for extracellular matrix in diminishing NET production was corroborated in vivo using a rat catheter model. The C. albicans pmr1Δ/Δ, defective in production of matrix mannan, appeared to elicit a greater abundance of NETs by scanning electron microscopy imaging, which correlated with a decreased fungal burden. Together, these findings show that C. albicans biofilms impair neutrophil response through an inhibitory pathway induced by the extracellular matrix. Public Library of Science 2016-09-13 /pmc/articles/PMC5021349/ /pubmed/27622514 http://dx.doi.org/10.1371/journal.ppat.1005884 Text en © 2016 Johnson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Johnson, Chad J. Cabezas-Olcoz, Jonathan Kernien, John F. Wang, Steven X. Beebe, David J. Huttenlocher, Anna Ansari, Hamayail Nett, Jeniel E. The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps |
title | The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps |
title_full | The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps |
title_fullStr | The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps |
title_full_unstemmed | The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps |
title_short | The Extracellular Matrix of Candida albicans Biofilms Impairs Formation of Neutrophil Extracellular Traps |
title_sort | extracellular matrix of candida albicans biofilms impairs formation of neutrophil extracellular traps |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021349/ https://www.ncbi.nlm.nih.gov/pubmed/27622514 http://dx.doi.org/10.1371/journal.ppat.1005884 |
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