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Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces

Due to the spread of resistance, antibiotic exposure receives increasing attention. Ecological consequences for the different niches of individual microbiomes are, however, largely ignored. Here, we report the effects of widely used antibiotics (clindamycin, ciprofloxacin, amoxicillin, and minocycli...

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Autores principales: Zaura, Egija, Brandt, Bernd W., Teixeira de Mattos, M. Joost, Buijs, Mark J., Caspers, Martien P. M., Rashid, Mamun-Ur, Weintraub, Andrej, Nord, Carl Erik, Savell, Ann, Hu, Yanmin, Coates, Antony R., Hubank, Mike, Spratt, David A., Wilson, Michael, Keijser, Bart J. F., Crielaard, Wim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659469/
https://www.ncbi.nlm.nih.gov/pubmed/26556275
http://dx.doi.org/10.1128/mBio.01693-15
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author Zaura, Egija
Brandt, Bernd W.
Teixeira de Mattos, M. Joost
Buijs, Mark J.
Caspers, Martien P. M.
Rashid, Mamun-Ur
Weintraub, Andrej
Nord, Carl Erik
Savell, Ann
Hu, Yanmin
Coates, Antony R.
Hubank, Mike
Spratt, David A.
Wilson, Michael
Keijser, Bart J. F.
Crielaard, Wim
author_facet Zaura, Egija
Brandt, Bernd W.
Teixeira de Mattos, M. Joost
Buijs, Mark J.
Caspers, Martien P. M.
Rashid, Mamun-Ur
Weintraub, Andrej
Nord, Carl Erik
Savell, Ann
Hu, Yanmin
Coates, Antony R.
Hubank, Mike
Spratt, David A.
Wilson, Michael
Keijser, Bart J. F.
Crielaard, Wim
author_sort Zaura, Egija
collection PubMed
description Due to the spread of resistance, antibiotic exposure receives increasing attention. Ecological consequences for the different niches of individual microbiomes are, however, largely ignored. Here, we report the effects of widely used antibiotics (clindamycin, ciprofloxacin, amoxicillin, and minocycline) with different modes of action on the ecology of both the gut and the oral microbiomes in 66 healthy adults from the United Kingdom and Sweden in a two-center randomized placebo-controlled clinical trial. Feces and saliva were collected at baseline, immediately after exposure, and 1, 2, 4, and 12 months after administration of antibiotics or placebo. Sequences of 16S rRNA gene amplicons from all samples and metagenomic shotgun sequences from selected baseline and post-antibiotic-treatment sample pairs were analyzed. Additionally, metagenomic predictions based on 16S rRNA gene amplicon data were performed using PICRUSt. The salivary microbiome was found to be significantly more robust, whereas the antibiotics negatively affected the fecal microbiome: in particular, health-associated butyrate-producing species became strongly underrepresented. Additionally, exposure to different antibiotics enriched genes associated with antibiotic resistance. In conclusion, healthy individuals, exposed to a single antibiotic treatment, undergo considerable microbial shifts and enrichment in antibiotic resistance in their feces, while their salivary microbiome composition remains unexpectedly stable. The health-related consequences for the gut microbiome should increase the awareness of the individual risks involved with antibiotic use, especially in a (diseased) population with an already dysregulated microbiome. On the other hand, understanding the mechanisms behind the resilience of the oral microbiome toward ecological collapse might prove useful in combating microbial dysbiosis elsewhere in the body.
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spelling pubmed-46594692015-12-02 Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces Zaura, Egija Brandt, Bernd W. Teixeira de Mattos, M. Joost Buijs, Mark J. Caspers, Martien P. M. Rashid, Mamun-Ur Weintraub, Andrej Nord, Carl Erik Savell, Ann Hu, Yanmin Coates, Antony R. Hubank, Mike Spratt, David A. Wilson, Michael Keijser, Bart J. F. Crielaard, Wim mBio Research Article Due to the spread of resistance, antibiotic exposure receives increasing attention. Ecological consequences for the different niches of individual microbiomes are, however, largely ignored. Here, we report the effects of widely used antibiotics (clindamycin, ciprofloxacin, amoxicillin, and minocycline) with different modes of action on the ecology of both the gut and the oral microbiomes in 66 healthy adults from the United Kingdom and Sweden in a two-center randomized placebo-controlled clinical trial. Feces and saliva were collected at baseline, immediately after exposure, and 1, 2, 4, and 12 months after administration of antibiotics or placebo. Sequences of 16S rRNA gene amplicons from all samples and metagenomic shotgun sequences from selected baseline and post-antibiotic-treatment sample pairs were analyzed. Additionally, metagenomic predictions based on 16S rRNA gene amplicon data were performed using PICRUSt. The salivary microbiome was found to be significantly more robust, whereas the antibiotics negatively affected the fecal microbiome: in particular, health-associated butyrate-producing species became strongly underrepresented. Additionally, exposure to different antibiotics enriched genes associated with antibiotic resistance. In conclusion, healthy individuals, exposed to a single antibiotic treatment, undergo considerable microbial shifts and enrichment in antibiotic resistance in their feces, while their salivary microbiome composition remains unexpectedly stable. The health-related consequences for the gut microbiome should increase the awareness of the individual risks involved with antibiotic use, especially in a (diseased) population with an already dysregulated microbiome. On the other hand, understanding the mechanisms behind the resilience of the oral microbiome toward ecological collapse might prove useful in combating microbial dysbiosis elsewhere in the body. American Society of Microbiology 2015-11-10 /pmc/articles/PMC4659469/ /pubmed/26556275 http://dx.doi.org/10.1128/mBio.01693-15 Text en Copyright © 2015 Zaura et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zaura, Egija
Brandt, Bernd W.
Teixeira de Mattos, M. Joost
Buijs, Mark J.
Caspers, Martien P. M.
Rashid, Mamun-Ur
Weintraub, Andrej
Nord, Carl Erik
Savell, Ann
Hu, Yanmin
Coates, Antony R.
Hubank, Mike
Spratt, David A.
Wilson, Michael
Keijser, Bart J. F.
Crielaard, Wim
Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces
title Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces
title_full Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces
title_fullStr Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces
title_full_unstemmed Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces
title_short Same Exposure but Two Radically Different Responses to Antibiotics: Resilience of the Salivary Microbiome versus Long-Term Microbial Shifts in Feces
title_sort same exposure but two radically different responses to antibiotics: resilience of the salivary microbiome versus long-term microbial shifts in feces
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659469/
https://www.ncbi.nlm.nih.gov/pubmed/26556275
http://dx.doi.org/10.1128/mBio.01693-15
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