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Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption
BACKGROUND: The microbiomes of animals are complex communities that strongly affect the health of the hosts. Microbiomes on mucosal surfaces have the highest densities and most extensive biochemical exchanges with the hosts. Although antibiotics are potent tools to manage infections, they can disrup...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388737/ https://www.ncbi.nlm.nih.gov/pubmed/30863123 http://dx.doi.org/10.2147/IDR.S185992 |
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author | Brumlow, Chelcy E Luna, Ruth A Hollister, Emily B Gomez, Javier A Burcham, Lindsey A Cowdrey, Madison B Primm, Todd P |
author_facet | Brumlow, Chelcy E Luna, Ruth A Hollister, Emily B Gomez, Javier A Burcham, Lindsey A Cowdrey, Madison B Primm, Todd P |
author_sort | Brumlow, Chelcy E |
collection | PubMed |
description | BACKGROUND: The microbiomes of animals are complex communities that strongly affect the health of the hosts. Microbiomes on mucosal surfaces have the highest densities and most extensive biochemical exchanges with the hosts. Although antibiotics are potent tools to manage infections, they can disrupt the normal microbiota, causing numerous side effects. MATERIALS AND METHODS: Taking a community ecology approach, mucosal microbiome community responses to five disruptive conditions (two broad-spectrum antibiotics, a biocide, elevated temperature, and rinsing) were analyzed. Skin of the fish Gambusia affinis was the mucosal model. Microbiome recovery was measured by culturable counts, community biochemical profiles, genetic fingerprinting, and community 16S gene sequencing (rinsing condition only). RESULTS: Following all disruptions, the total counts rose and then returned to the pre-treatment (PT) level. This overgrowth was confirmed via direct staining and community metabolic activity measurements. After rinsing, diversity decreased and one taxon dominated (family Aeromonadaceae) temporarily, the findings similar to numerous other studies with antibiotics. While the community did not return to the PT taxonomic composition, the biochemical profile did. CONCLUSION: This suggests that the biochemical pathways in a community are important during recovery, and a return to the original composition is not required to restore original function. |
format | Online Article Text |
id | pubmed-6388737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63887372019-03-12 Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption Brumlow, Chelcy E Luna, Ruth A Hollister, Emily B Gomez, Javier A Burcham, Lindsey A Cowdrey, Madison B Primm, Todd P Infect Drug Resist Original Research BACKGROUND: The microbiomes of animals are complex communities that strongly affect the health of the hosts. Microbiomes on mucosal surfaces have the highest densities and most extensive biochemical exchanges with the hosts. Although antibiotics are potent tools to manage infections, they can disrupt the normal microbiota, causing numerous side effects. MATERIALS AND METHODS: Taking a community ecology approach, mucosal microbiome community responses to five disruptive conditions (two broad-spectrum antibiotics, a biocide, elevated temperature, and rinsing) were analyzed. Skin of the fish Gambusia affinis was the mucosal model. Microbiome recovery was measured by culturable counts, community biochemical profiles, genetic fingerprinting, and community 16S gene sequencing (rinsing condition only). RESULTS: Following all disruptions, the total counts rose and then returned to the pre-treatment (PT) level. This overgrowth was confirmed via direct staining and community metabolic activity measurements. After rinsing, diversity decreased and one taxon dominated (family Aeromonadaceae) temporarily, the findings similar to numerous other studies with antibiotics. While the community did not return to the PT taxonomic composition, the biochemical profile did. CONCLUSION: This suggests that the biochemical pathways in a community are important during recovery, and a return to the original composition is not required to restore original function. Dove Medical Press 2019-02-13 /pmc/articles/PMC6388737/ /pubmed/30863123 http://dx.doi.org/10.2147/IDR.S185992 Text en © 2019 Brumlow et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Brumlow, Chelcy E Luna, Ruth A Hollister, Emily B Gomez, Javier A Burcham, Lindsey A Cowdrey, Madison B Primm, Todd P Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
title | Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
title_full | Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
title_fullStr | Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
title_full_unstemmed | Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
title_short | Biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
title_sort | biochemical but not compositional recovery of skin mucosal microbiome communities after disruption |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388737/ https://www.ncbi.nlm.nih.gov/pubmed/30863123 http://dx.doi.org/10.2147/IDR.S185992 |
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