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Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota

The adaptive evolution in indigenous intestinal microbes derived from probiotics is critical to safety and efficacy evaluation of probiotics, yet it is still largely underexplored. Here, through 11 publicly accessible datasets, we demonstrated that probiotic consumption can lead to widespread single...

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Autores principales: Ma, Chenchen, Zhang, Chengcheng, Chen, Denghui, Jiang, Shuaiming, Shen, Siyuan, Huo, Dongxue, Huang, Shi, Zhai, Qixiao, Zhang, Jiachao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523657/
https://www.ncbi.nlm.nih.gov/pubmed/34663913
http://dx.doi.org/10.1038/s42003-021-02724-8
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author Ma, Chenchen
Zhang, Chengcheng
Chen, Denghui
Jiang, Shuaiming
Shen, Siyuan
Huo, Dongxue
Huang, Shi
Zhai, Qixiao
Zhang, Jiachao
author_facet Ma, Chenchen
Zhang, Chengcheng
Chen, Denghui
Jiang, Shuaiming
Shen, Siyuan
Huo, Dongxue
Huang, Shi
Zhai, Qixiao
Zhang, Jiachao
author_sort Ma, Chenchen
collection PubMed
description The adaptive evolution in indigenous intestinal microbes derived from probiotics is critical to safety and efficacy evaluation of probiotics, yet it is still largely underexplored. Here, through 11 publicly accessible datasets, we demonstrated that probiotic consumption can lead to widespread single-nucleotide variants (SNVs) in the native microbiota. Interestingly, the same probiotic strains introduced far more SNVs in mouse gut than humans. Furthermore, the pattern of probiotics-induced SNVs was highly probiotic-strain specific, and 17 common SNVs in Faecalibacterium prausnitzii genome were identified cross studies, which might lead to changes in bacterial protein structure. Further, nearly 50% of F. prausnitzii SNVs can be inherited for six months in an independent human cohort, whereas the other half only transiently occurred. Collectively, our study substantially extended our understanding of co-evolution of the probiotics and the indigenous gut microbiota, highlighting the importance of assessment of probiotics efficacy and safety in an integrated manner.
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spelling pubmed-85236572021-11-15 Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota Ma, Chenchen Zhang, Chengcheng Chen, Denghui Jiang, Shuaiming Shen, Siyuan Huo, Dongxue Huang, Shi Zhai, Qixiao Zhang, Jiachao Commun Biol Article The adaptive evolution in indigenous intestinal microbes derived from probiotics is critical to safety and efficacy evaluation of probiotics, yet it is still largely underexplored. Here, through 11 publicly accessible datasets, we demonstrated that probiotic consumption can lead to widespread single-nucleotide variants (SNVs) in the native microbiota. Interestingly, the same probiotic strains introduced far more SNVs in mouse gut than humans. Furthermore, the pattern of probiotics-induced SNVs was highly probiotic-strain specific, and 17 common SNVs in Faecalibacterium prausnitzii genome were identified cross studies, which might lead to changes in bacterial protein structure. Further, nearly 50% of F. prausnitzii SNVs can be inherited for six months in an independent human cohort, whereas the other half only transiently occurred. Collectively, our study substantially extended our understanding of co-evolution of the probiotics and the indigenous gut microbiota, highlighting the importance of assessment of probiotics efficacy and safety in an integrated manner. Nature Publishing Group UK 2021-10-18 /pmc/articles/PMC8523657/ /pubmed/34663913 http://dx.doi.org/10.1038/s42003-021-02724-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ma, Chenchen
Zhang, Chengcheng
Chen, Denghui
Jiang, Shuaiming
Shen, Siyuan
Huo, Dongxue
Huang, Shi
Zhai, Qixiao
Zhang, Jiachao
Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
title Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
title_full Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
title_fullStr Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
title_full_unstemmed Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
title_short Probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
title_sort probiotic consumption influences universal adaptive mutations in indigenous human and mouse gut microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523657/
https://www.ncbi.nlm.nih.gov/pubmed/34663913
http://dx.doi.org/10.1038/s42003-021-02724-8
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