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Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults
Antibiotics are deployed against bacterial pathogens, but their targeting of conserved microbial processes means they also collaterally perturb the commensal microbiome. To understand acute and persistent effects of antibiotics on the gut microbiota of healthy adult volunteers, we quantify microbiom...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066705/ https://www.ncbi.nlm.nih.gov/pubmed/35417701 http://dx.doi.org/10.1016/j.celrep.2022.110649 |
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author | Anthony, Winston E. Wang, Bin Sukhum, Kimberley V. D’Souza, Alaric W. Hink, Tiffany Cass, Candice Seiler, Sondra Reske, Kimberly A. Coon, Christopher Dubberke, Erik R. Burnham, Carey-Ann D. Dantas, Gautam Kwon, Jennie H. |
author_facet | Anthony, Winston E. Wang, Bin Sukhum, Kimberley V. D’Souza, Alaric W. Hink, Tiffany Cass, Candice Seiler, Sondra Reske, Kimberly A. Coon, Christopher Dubberke, Erik R. Burnham, Carey-Ann D. Dantas, Gautam Kwon, Jennie H. |
author_sort | Anthony, Winston E. |
collection | PubMed |
description | Antibiotics are deployed against bacterial pathogens, but their targeting of conserved microbial processes means they also collaterally perturb the commensal microbiome. To understand acute and persistent effects of antibiotics on the gut microbiota of healthy adult volunteers, we quantify microbiome dynamics before, during, and 6 months after exposure to 4 commonly used antibiotic regimens. We observe an acute decrease in species richness and culturable bacteria after antibiotics, with most healthy adult microbiomes returning to pre-treatment species richness after 2 months, but with an altered taxonomy, resistome, and metabolic output, as well as an increased antibiotic resistance burden. Azithromycin delays the recovery of species richness, resulting in greater compositional distance. A subset of volunteers experience a persistent reduction in microbiome diversity after antibiotics and share compositional similarities with patients hospitalized in intensive care units. These results improve our quantitative understanding of the impact of antibiotics on commensal microbiome dynamics, resilience, and recovery. |
format | Online Article Text |
id | pubmed-9066705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-90667052022-05-03 Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults Anthony, Winston E. Wang, Bin Sukhum, Kimberley V. D’Souza, Alaric W. Hink, Tiffany Cass, Candice Seiler, Sondra Reske, Kimberly A. Coon, Christopher Dubberke, Erik R. Burnham, Carey-Ann D. Dantas, Gautam Kwon, Jennie H. Cell Rep Article Antibiotics are deployed against bacterial pathogens, but their targeting of conserved microbial processes means they also collaterally perturb the commensal microbiome. To understand acute and persistent effects of antibiotics on the gut microbiota of healthy adult volunteers, we quantify microbiome dynamics before, during, and 6 months after exposure to 4 commonly used antibiotic regimens. We observe an acute decrease in species richness and culturable bacteria after antibiotics, with most healthy adult microbiomes returning to pre-treatment species richness after 2 months, but with an altered taxonomy, resistome, and metabolic output, as well as an increased antibiotic resistance burden. Azithromycin delays the recovery of species richness, resulting in greater compositional distance. A subset of volunteers experience a persistent reduction in microbiome diversity after antibiotics and share compositional similarities with patients hospitalized in intensive care units. These results improve our quantitative understanding of the impact of antibiotics on commensal microbiome dynamics, resilience, and recovery. 2022-04-12 /pmc/articles/PMC9066705/ /pubmed/35417701 http://dx.doi.org/10.1016/j.celrep.2022.110649 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Anthony, Winston E. Wang, Bin Sukhum, Kimberley V. D’Souza, Alaric W. Hink, Tiffany Cass, Candice Seiler, Sondra Reske, Kimberly A. Coon, Christopher Dubberke, Erik R. Burnham, Carey-Ann D. Dantas, Gautam Kwon, Jennie H. Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
title | Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
title_full | Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
title_fullStr | Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
title_full_unstemmed | Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
title_short | Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
title_sort | acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066705/ https://www.ncbi.nlm.nih.gov/pubmed/35417701 http://dx.doi.org/10.1016/j.celrep.2022.110649 |
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