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Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome

Nonhealing chronic wounds are all unique in origin and circumstance, and attempting to isolate a single etiology for the failure of a wound to heal is daunting. Wounds represent complex systems of multispecies fungal and bacterial biofilms. The survival strategies of interactive microbial communitie...

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Autor principal: Ghannoum, Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111414/
https://www.ncbi.nlm.nih.gov/pubmed/27935844
http://dx.doi.org/10.1128/mBio.01951-16
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author Ghannoum, Mahmoud
author_facet Ghannoum, Mahmoud
author_sort Ghannoum, Mahmoud
collection PubMed
description Nonhealing chronic wounds are all unique in origin and circumstance, and attempting to isolate a single etiology for the failure of a wound to heal is daunting. Wounds represent complex systems of multispecies fungal and bacterial biofilms. The survival strategies of interactive microbial communities have led to cooperative evolutionary strategies that culminate in biofilm formation. In microbial dysbiosis, biofilms are beneficial to both bacterial and fungal communities but detrimental to the host. Fungi benefit by a surge in their virulence factors, while bacteria become tolerant to antibacterials as a consequence of living under the protective umbrella of the biofilm matrix. This interkingdom cooperation negatively impacts the host, as the fungi and bacteria produce extracellular enzymes that inflict tissue damage, leading to an increase in proinflammatory cytokines, which results in oxidative damage and apoptotic cell death.
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spelling pubmed-51114142016-11-18 Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome Ghannoum, Mahmoud mBio Commentary Nonhealing chronic wounds are all unique in origin and circumstance, and attempting to isolate a single etiology for the failure of a wound to heal is daunting. Wounds represent complex systems of multispecies fungal and bacterial biofilms. The survival strategies of interactive microbial communities have led to cooperative evolutionary strategies that culminate in biofilm formation. In microbial dysbiosis, biofilms are beneficial to both bacterial and fungal communities but detrimental to the host. Fungi benefit by a surge in their virulence factors, while bacteria become tolerant to antibacterials as a consequence of living under the protective umbrella of the biofilm matrix. This interkingdom cooperation negatively impacts the host, as the fungi and bacteria produce extracellular enzymes that inflict tissue damage, leading to an increase in proinflammatory cytokines, which results in oxidative damage and apoptotic cell death. American Society for Microbiology 2016-11-15 /pmc/articles/PMC5111414/ /pubmed/27935844 http://dx.doi.org/10.1128/mBio.01951-16 Text en Copyright © 2016 Ghannoum. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Ghannoum, Mahmoud
Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome
title Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome
title_full Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome
title_fullStr Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome
title_full_unstemmed Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome
title_short Cooperative Evolutionary Strategy between the Bacteriome and Mycobiome
title_sort cooperative evolutionary strategy between the bacteriome and mycobiome
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111414/
https://www.ncbi.nlm.nih.gov/pubmed/27935844
http://dx.doi.org/10.1128/mBio.01951-16
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