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Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children

The gut microbiome represents an important reservoir of antibiotic resistance genes (ARGs). Effective methods are urgently needed for managing the gut resistome to fight against the antibiotic resistance threat. In this study, we show that a gut microbiota-targeted dietary intervention, which shifts...

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Autores principales: Wu, Guojun, Zhang, Chenhong, Wang, Jing, Zhang, Feng, Wang, Ruirui, Shen, Jian, Wang, Linghua, Pang, Xiaoyan, Zhang, Xiaojun, Zhao, Liping, Zhang, Menghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820771/
https://www.ncbi.nlm.nih.gov/pubmed/27044409
http://dx.doi.org/10.1038/srep24030
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author Wu, Guojun
Zhang, Chenhong
Wang, Jing
Zhang, Feng
Wang, Ruirui
Shen, Jian
Wang, Linghua
Pang, Xiaoyan
Zhang, Xiaojun
Zhao, Liping
Zhang, Menghui
author_facet Wu, Guojun
Zhang, Chenhong
Wang, Jing
Zhang, Feng
Wang, Ruirui
Shen, Jian
Wang, Linghua
Pang, Xiaoyan
Zhang, Xiaojun
Zhao, Liping
Zhang, Menghui
author_sort Wu, Guojun
collection PubMed
description The gut microbiome represents an important reservoir of antibiotic resistance genes (ARGs). Effective methods are urgently needed for managing the gut resistome to fight against the antibiotic resistance threat. In this study, we show that a gut microbiota-targeted dietary intervention, which shifts the dominant fermentation of gut bacteria from protein to carbohydrate, significantly diminished the gut resistome and alleviated metabolic syndrome in obese children. Of the non-redundant metagenomic gene catalog of ~2 × 10(6) microbial genes, 399 ARGs were identified in 131 gene types and conferred resistance to 47 antibiotics. Both the richness and diversity of the gut resistome were significantly reduced after the intervention. A total of 201 of the 399 ARGs were carried in 120 co-abundance gene groups (CAGs) directly binned from the gene catalog across both pre-and post-intervention samples. The intervention significantly reduced several CAGs in Klebsiella, Enterobacter and Escherichia, which were the major hubs for multiple resistance gene types. Thus, dietary intervention may become a potentially effective method for diminishing the gut resistome.
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spelling pubmed-48207712016-04-06 Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children Wu, Guojun Zhang, Chenhong Wang, Jing Zhang, Feng Wang, Ruirui Shen, Jian Wang, Linghua Pang, Xiaoyan Zhang, Xiaojun Zhao, Liping Zhang, Menghui Sci Rep Article The gut microbiome represents an important reservoir of antibiotic resistance genes (ARGs). Effective methods are urgently needed for managing the gut resistome to fight against the antibiotic resistance threat. In this study, we show that a gut microbiota-targeted dietary intervention, which shifts the dominant fermentation of gut bacteria from protein to carbohydrate, significantly diminished the gut resistome and alleviated metabolic syndrome in obese children. Of the non-redundant metagenomic gene catalog of ~2 × 10(6) microbial genes, 399 ARGs were identified in 131 gene types and conferred resistance to 47 antibiotics. Both the richness and diversity of the gut resistome were significantly reduced after the intervention. A total of 201 of the 399 ARGs were carried in 120 co-abundance gene groups (CAGs) directly binned from the gene catalog across both pre-and post-intervention samples. The intervention significantly reduced several CAGs in Klebsiella, Enterobacter and Escherichia, which were the major hubs for multiple resistance gene types. Thus, dietary intervention may become a potentially effective method for diminishing the gut resistome. Nature Publishing Group 2016-04-05 /pmc/articles/PMC4820771/ /pubmed/27044409 http://dx.doi.org/10.1038/srep24030 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wu, Guojun
Zhang, Chenhong
Wang, Jing
Zhang, Feng
Wang, Ruirui
Shen, Jian
Wang, Linghua
Pang, Xiaoyan
Zhang, Xiaojun
Zhao, Liping
Zhang, Menghui
Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
title Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
title_full Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
title_fullStr Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
title_full_unstemmed Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
title_short Diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
title_sort diminution of the gut resistome after a gut microbiota-targeted dietary intervention in obese children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820771/
https://www.ncbi.nlm.nih.gov/pubmed/27044409
http://dx.doi.org/10.1038/srep24030
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