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Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria
BACKGROUND: Antibiotic-resistant (AR) bacteria are a global threat. AR bacteria can be acquired in early life and have long-term sequelae. Limiting the spread of antibiotic resistance without triggering the development of additional resistance mechanisms is of immense clinical value. Here, we show h...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693174/ https://www.ncbi.nlm.nih.gov/pubmed/31423298 http://dx.doi.org/10.1186/s13756-019-0583-6 |
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author | Casaburi, Giorgio Duar, Rebbeca M. Vance, Daniel P. Mitchell, Ryan Contreras, Lindsey Frese, Steven A. Smilowitz, Jennifer T. Underwood, Mark A. |
author_facet | Casaburi, Giorgio Duar, Rebbeca M. Vance, Daniel P. Mitchell, Ryan Contreras, Lindsey Frese, Steven A. Smilowitz, Jennifer T. Underwood, Mark A. |
author_sort | Casaburi, Giorgio |
collection | PubMed |
description | BACKGROUND: Antibiotic-resistant (AR) bacteria are a global threat. AR bacteria can be acquired in early life and have long-term sequelae. Limiting the spread of antibiotic resistance without triggering the development of additional resistance mechanisms is of immense clinical value. Here, we show how the infant gut microbiome can be modified, resulting in a significant reduction of AR genes (ARGs) and the potentially pathogenic bacteria that harbor them. METHODS: The gut microbiome was characterized using shotgun metagenomics of fecal samples from two groups of healthy, term breastfed infants. One group was fed B. infantis EVC001 in addition to receiving lactation support (n = 29, EVC001-fed), while the other received lactation support alone (n = 31, controls). Coliforms were isolated from fecal samples and genome sequenced, as well as tested for minimal inhibitory concentrations against clinically relevant antibiotics. RESULTS: Infants fed B. infantis EVC001 exhibited a change to the gut microbiome, resulting in a 90% lower level of ARGs compared to controls. ARGs that differed significantly between groups were predicted to confer resistance to beta lactams, fluoroquinolones, or multiple drug classes, the majority of which belonged to Escherichia, Clostridium, and Staphylococcus. Minimal inhibitory concentration assays confirmed the resistance phenotypes among isolates with these genes. Notably, we found extended-spectrum beta lactamases among healthy, vaginally delivered breastfed infants who had never been exposed to antibiotics. CONCLUSIONS: Colonization of the gut of breastfed infants by a single strain of B. longum subsp. infantis had a profound impact on the fecal metagenome, including a reduction in ARGs. This highlights the importance of developing novel approaches to limit the spread of these genes among clinically relevant bacteria. Future studies are needed to determine whether colonization with B. infantis EVC001 decreases the incidence of AR infections in breastfed infants. TRIAL REGISTRATION: This clinical trial was registered at ClinicalTrials.gov, NCT02457338. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13756-019-0583-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6693174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66931742019-08-16 Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria Casaburi, Giorgio Duar, Rebbeca M. Vance, Daniel P. Mitchell, Ryan Contreras, Lindsey Frese, Steven A. Smilowitz, Jennifer T. Underwood, Mark A. Antimicrob Resist Infect Control Research BACKGROUND: Antibiotic-resistant (AR) bacteria are a global threat. AR bacteria can be acquired in early life and have long-term sequelae. Limiting the spread of antibiotic resistance without triggering the development of additional resistance mechanisms is of immense clinical value. Here, we show how the infant gut microbiome can be modified, resulting in a significant reduction of AR genes (ARGs) and the potentially pathogenic bacteria that harbor them. METHODS: The gut microbiome was characterized using shotgun metagenomics of fecal samples from two groups of healthy, term breastfed infants. One group was fed B. infantis EVC001 in addition to receiving lactation support (n = 29, EVC001-fed), while the other received lactation support alone (n = 31, controls). Coliforms were isolated from fecal samples and genome sequenced, as well as tested for minimal inhibitory concentrations against clinically relevant antibiotics. RESULTS: Infants fed B. infantis EVC001 exhibited a change to the gut microbiome, resulting in a 90% lower level of ARGs compared to controls. ARGs that differed significantly between groups were predicted to confer resistance to beta lactams, fluoroquinolones, or multiple drug classes, the majority of which belonged to Escherichia, Clostridium, and Staphylococcus. Minimal inhibitory concentration assays confirmed the resistance phenotypes among isolates with these genes. Notably, we found extended-spectrum beta lactamases among healthy, vaginally delivered breastfed infants who had never been exposed to antibiotics. CONCLUSIONS: Colonization of the gut of breastfed infants by a single strain of B. longum subsp. infantis had a profound impact on the fecal metagenome, including a reduction in ARGs. This highlights the importance of developing novel approaches to limit the spread of these genes among clinically relevant bacteria. Future studies are needed to determine whether colonization with B. infantis EVC001 decreases the incidence of AR infections in breastfed infants. TRIAL REGISTRATION: This clinical trial was registered at ClinicalTrials.gov, NCT02457338. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13756-019-0583-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-14 /pmc/articles/PMC6693174/ /pubmed/31423298 http://dx.doi.org/10.1186/s13756-019-0583-6 Text en © The Author(s). 2019 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 | Research Casaburi, Giorgio Duar, Rebbeca M. Vance, Daniel P. Mitchell, Ryan Contreras, Lindsey Frese, Steven A. Smilowitz, Jennifer T. Underwood, Mark A. Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
title | Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
title_full | Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
title_fullStr | Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
title_full_unstemmed | Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
title_short | Early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
title_sort | early-life gut microbiome modulation reduces the abundance of antibiotic-resistant bacteria |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693174/ https://www.ncbi.nlm.nih.gov/pubmed/31423298 http://dx.doi.org/10.1186/s13756-019-0583-6 |
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