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Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance

Antibiotic treatment can lead to a loss of diversity of gut microbiota and may adversely affect gut microbiota composition and host health. Previous studies have indicated that the recovery of gut microbes from antibiotic-induced disruption may be guided by specific microbial species. We expect to p...

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Autores principales: Chen, Jing, Zhu, Jinlin, Lu, Wenwei, Wang, Hongchao, Pan, Mingluo, Tian, Peijun, Zhao, Jianxin, Zhang, Hao, Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10536327/
https://www.ncbi.nlm.nih.gov/pubmed/37764709
http://dx.doi.org/10.3390/nu15183925
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author Chen, Jing
Zhu, Jinlin
Lu, Wenwei
Wang, Hongchao
Pan, Mingluo
Tian, Peijun
Zhao, Jianxin
Zhang, Hao
Chen, Wei
author_facet Chen, Jing
Zhu, Jinlin
Lu, Wenwei
Wang, Hongchao
Pan, Mingluo
Tian, Peijun
Zhao, Jianxin
Zhang, Hao
Chen, Wei
author_sort Chen, Jing
collection PubMed
description Antibiotic treatment can lead to a loss of diversity of gut microbiota and may adversely affect gut microbiota composition and host health. Previous studies have indicated that the recovery of gut microbes from antibiotic-induced disruption may be guided by specific microbial species. We expect to predict recovery or non-recovery using these crucial species or other indices after antibiotic treatment only when the gut microbiota changes. This study focused on this prediction problem using a novel ensemble learning framework to identify a set of common and reasonably predictive recovery-associated bacterial species (p-RABs), enabling us to predict the host microbiome recovery status under broad-spectrum antibiotic treatment. Our findings also propose other predictive indicators, suggesting that higher taxonomic and functional diversity may correlate with an increased likelihood of successful recovery. Furthermore, to explore the validity of p-RABs, we performed a metabolic support analysis and identified Akkermansia muciniphila and Bacteroides uniformis as potential key supporting species for reconstruction interventions. Experimental results from a C57BL/6J male mouse model demonstrated the effectiveness of p-RABs in facilitating intestinal microbial reconstitution. Thus, we proved the reliability of the new p-RABs and validated a practical intervention scheme for gut microbiota reconstruction under antibiotic disturbance.
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spelling pubmed-105363272023-09-29 Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance Chen, Jing Zhu, Jinlin Lu, Wenwei Wang, Hongchao Pan, Mingluo Tian, Peijun Zhao, Jianxin Zhang, Hao Chen, Wei Nutrients Article Antibiotic treatment can lead to a loss of diversity of gut microbiota and may adversely affect gut microbiota composition and host health. Previous studies have indicated that the recovery of gut microbes from antibiotic-induced disruption may be guided by specific microbial species. We expect to predict recovery or non-recovery using these crucial species or other indices after antibiotic treatment only when the gut microbiota changes. This study focused on this prediction problem using a novel ensemble learning framework to identify a set of common and reasonably predictive recovery-associated bacterial species (p-RABs), enabling us to predict the host microbiome recovery status under broad-spectrum antibiotic treatment. Our findings also propose other predictive indicators, suggesting that higher taxonomic and functional diversity may correlate with an increased likelihood of successful recovery. Furthermore, to explore the validity of p-RABs, we performed a metabolic support analysis and identified Akkermansia muciniphila and Bacteroides uniformis as potential key supporting species for reconstruction interventions. Experimental results from a C57BL/6J male mouse model demonstrated the effectiveness of p-RABs in facilitating intestinal microbial reconstitution. Thus, we proved the reliability of the new p-RABs and validated a practical intervention scheme for gut microbiota reconstruction under antibiotic disturbance. MDPI 2023-09-10 /pmc/articles/PMC10536327/ /pubmed/37764709 http://dx.doi.org/10.3390/nu15183925 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Jing
Zhu, Jinlin
Lu, Wenwei
Wang, Hongchao
Pan, Mingluo
Tian, Peijun
Zhao, Jianxin
Zhang, Hao
Chen, Wei
Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance
title Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance
title_full Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance
title_fullStr Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance
title_full_unstemmed Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance
title_short Uncovering Predictive Factors and Interventions for Restoring Microecological Diversity after Antibiotic Disturbance
title_sort uncovering predictive factors and interventions for restoring microecological diversity after antibiotic disturbance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10536327/
https://www.ncbi.nlm.nih.gov/pubmed/37764709
http://dx.doi.org/10.3390/nu15183925
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