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Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice

Fecal microbiota transplantation (FMT) of human fecal samples into germ-free (GF) mice is useful for establishing causal relationships between the gut microbiota and human phenotypes. However, due to the intrinsic differences between human and mouse intestines and the different diets of the two orga...

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Autores principales: Li, Yanze, Cao, Wenming, Gao, Na L, Zhao, Xing-Ming, Chen, Wei-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684084/
https://www.ncbi.nlm.nih.gov/pubmed/34118462
http://dx.doi.org/10.1016/j.gpb.2020.06.024
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author Li, Yanze
Cao, Wenming
Gao, Na L
Zhao, Xing-Ming
Chen, Wei-Hua
author_facet Li, Yanze
Cao, Wenming
Gao, Na L
Zhao, Xing-Ming
Chen, Wei-Hua
author_sort Li, Yanze
collection PubMed
description Fecal microbiota transplantation (FMT) of human fecal samples into germ-free (GF) mice is useful for establishing causal relationships between the gut microbiota and human phenotypes. However, due to the intrinsic differences between human and mouse intestines and the different diets of the two organisms, it may not be possible to replicate human phenotypes in mice through FMT; similarly, treatments that are effective in mouse models may not be effective in humans. In this study, we aimed to identify human gut microbes that undergo significant and consistent changes (i.e., in relative abundances) after transplantation into GF mice in multiple experimental settings. We collected 16S rDNA-seq data from four published studies and analyzed the gut microbiota profiles from 1713 human–mouse pairs. Strikingly, on average, we found that only 47% of the human gut microbes could be re-established in mice at the species level, among which more than 1/3 underwent significant changes (referred to as “variable taxa”). Most of the human gut microbes that underwent significant changes were consistent across multiple human–mouse pairs and experimental settings. Consequently, about 1/3 of human samples changed their enterotypes, i.e., significant changes in their leading species after FMT. Mice fed with a controlled diet showed a lower enterotype change rate (23.5%) than those fed with a noncontrolled diet (49.0%), suggesting a possible solution for rescue. Most of the variable taxa have been reported to be implicated in human diseases, with some recognized as the causative species. Our results highlight the challenges of using a mouse model to replicate human gut microbiota-associated phenotypes, provide useful information for researchers using mice in gut microbiota studies, and call for additional validations after FMT. An online database named FMT-DB is publicly available at http://fmt2mice.humangut.info/#/.
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spelling pubmed-96840842022-11-25 Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice Li, Yanze Cao, Wenming Gao, Na L Zhao, Xing-Ming Chen, Wei-Hua Genomics Proteomics Bioinformatics Original Research Fecal microbiota transplantation (FMT) of human fecal samples into germ-free (GF) mice is useful for establishing causal relationships between the gut microbiota and human phenotypes. However, due to the intrinsic differences between human and mouse intestines and the different diets of the two organisms, it may not be possible to replicate human phenotypes in mice through FMT; similarly, treatments that are effective in mouse models may not be effective in humans. In this study, we aimed to identify human gut microbes that undergo significant and consistent changes (i.e., in relative abundances) after transplantation into GF mice in multiple experimental settings. We collected 16S rDNA-seq data from four published studies and analyzed the gut microbiota profiles from 1713 human–mouse pairs. Strikingly, on average, we found that only 47% of the human gut microbes could be re-established in mice at the species level, among which more than 1/3 underwent significant changes (referred to as “variable taxa”). Most of the human gut microbes that underwent significant changes were consistent across multiple human–mouse pairs and experimental settings. Consequently, about 1/3 of human samples changed their enterotypes, i.e., significant changes in their leading species after FMT. Mice fed with a controlled diet showed a lower enterotype change rate (23.5%) than those fed with a noncontrolled diet (49.0%), suggesting a possible solution for rescue. Most of the variable taxa have been reported to be implicated in human diseases, with some recognized as the causative species. Our results highlight the challenges of using a mouse model to replicate human gut microbiota-associated phenotypes, provide useful information for researchers using mice in gut microbiota studies, and call for additional validations after FMT. An online database named FMT-DB is publicly available at http://fmt2mice.humangut.info/#/. Elsevier 2022-04 2021-06-09 /pmc/articles/PMC9684084/ /pubmed/34118462 http://dx.doi.org/10.1016/j.gpb.2020.06.024 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Li, Yanze
Cao, Wenming
Gao, Na L
Zhao, Xing-Ming
Chen, Wei-Hua
Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice
title Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice
title_full Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice
title_fullStr Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice
title_full_unstemmed Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice
title_short Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-free Mice
title_sort consistent alterations of human fecal microbes after transplantation into germ-free mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684084/
https://www.ncbi.nlm.nih.gov/pubmed/34118462
http://dx.doi.org/10.1016/j.gpb.2020.06.024
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