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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
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.
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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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