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The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation

The widespread use of antibiotics in the past 80 years has saved millions of human lives, facilitated technological progress and killed incalculable numbers of microbes, both pathogenic and commensal. Human-associated microbes perform an array of important functions, and we are now just beginning to...

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Autores principales: Langdon, Amy, Crook, Nathan, Dantas, Gautam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831151/
https://www.ncbi.nlm.nih.gov/pubmed/27074706
http://dx.doi.org/10.1186/s13073-016-0294-z
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author Langdon, Amy
Crook, Nathan
Dantas, Gautam
author_facet Langdon, Amy
Crook, Nathan
Dantas, Gautam
author_sort Langdon, Amy
collection PubMed
description The widespread use of antibiotics in the past 80 years has saved millions of human lives, facilitated technological progress and killed incalculable numbers of microbes, both pathogenic and commensal. Human-associated microbes perform an array of important functions, and we are now just beginning to understand the ways in which antibiotics have reshaped their ecology and the functional consequences of these changes. Mounting evidence shows that antibiotics influence the function of the immune system, our ability to resist infection, and our capacity for processing food. Therefore, it is now more important than ever to revisit how we use antibiotics. This review summarizes current research on the short-term and long-term consequences of antibiotic use on the human microbiome, from early life to adulthood, and its effect on diseases such as malnutrition, obesity, diabetes, and Clostridium difficile infection. Motivated by the consequences of inappropriate antibiotic use, we explore recent progress in the development of antivirulence approaches for resisting infection while minimizing resistance to therapy. We close the article by discussing probiotics and fecal microbiota transplants, which promise to restore the microbiota after damage of the microbiome. Together, the results of studies in this field emphasize the importance of developing a mechanistic understanding of gut ecology to enable the development of new therapeutic strategies and to rationally limit the use of antibiotic compounds.
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spelling pubmed-48311512016-04-15 The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation Langdon, Amy Crook, Nathan Dantas, Gautam Genome Med Review The widespread use of antibiotics in the past 80 years has saved millions of human lives, facilitated technological progress and killed incalculable numbers of microbes, both pathogenic and commensal. Human-associated microbes perform an array of important functions, and we are now just beginning to understand the ways in which antibiotics have reshaped their ecology and the functional consequences of these changes. Mounting evidence shows that antibiotics influence the function of the immune system, our ability to resist infection, and our capacity for processing food. Therefore, it is now more important than ever to revisit how we use antibiotics. This review summarizes current research on the short-term and long-term consequences of antibiotic use on the human microbiome, from early life to adulthood, and its effect on diseases such as malnutrition, obesity, diabetes, and Clostridium difficile infection. Motivated by the consequences of inappropriate antibiotic use, we explore recent progress in the development of antivirulence approaches for resisting infection while minimizing resistance to therapy. We close the article by discussing probiotics and fecal microbiota transplants, which promise to restore the microbiota after damage of the microbiome. Together, the results of studies in this field emphasize the importance of developing a mechanistic understanding of gut ecology to enable the development of new therapeutic strategies and to rationally limit the use of antibiotic compounds. BioMed Central 2016-04-13 /pmc/articles/PMC4831151/ /pubmed/27074706 http://dx.doi.org/10.1186/s13073-016-0294-z Text en © Langdon et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Langdon, Amy
Crook, Nathan
Dantas, Gautam
The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
title The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
title_full The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
title_fullStr The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
title_full_unstemmed The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
title_short The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
title_sort effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831151/
https://www.ncbi.nlm.nih.gov/pubmed/27074706
http://dx.doi.org/10.1186/s13073-016-0294-z
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