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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8523657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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