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Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice

Probiotics are intended to improve gastrointestinal health when consumed. However, the probiotics marketed today only colonize the densely populated gut to a limited extent. Bacteriophages comprise the majority of viruses in the human gut virome and there are strong indications that they play import...

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Autores principales: Rasmussen, Torben Sølbeck, Mentzel, Caroline M. Junker, Danielsen, Malene Refslund, Jakobsen, Rasmus Riemer, Zachariassen, Line Sidsel Fisker, Castro Mejia, Josue Leonardo, Brunse, Anders, Hansen, Lars Hestbjerg, Hansen, Camilla Hartmann Friis, Hansen, Axel Kornerup, Nielsen, Dennis Sandris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167882/
https://www.ncbi.nlm.nih.gov/pubmed/37150906
http://dx.doi.org/10.1080/19490976.2023.2208504
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author Rasmussen, Torben Sølbeck
Mentzel, Caroline M. Junker
Danielsen, Malene Refslund
Jakobsen, Rasmus Riemer
Zachariassen, Line Sidsel Fisker
Castro Mejia, Josue Leonardo
Brunse, Anders
Hansen, Lars Hestbjerg
Hansen, Camilla Hartmann Friis
Hansen, Axel Kornerup
Nielsen, Dennis Sandris
author_facet Rasmussen, Torben Sølbeck
Mentzel, Caroline M. Junker
Danielsen, Malene Refslund
Jakobsen, Rasmus Riemer
Zachariassen, Line Sidsel Fisker
Castro Mejia, Josue Leonardo
Brunse, Anders
Hansen, Lars Hestbjerg
Hansen, Camilla Hartmann Friis
Hansen, Axel Kornerup
Nielsen, Dennis Sandris
author_sort Rasmussen, Torben Sølbeck
collection PubMed
description Probiotics are intended to improve gastrointestinal health when consumed. However, the probiotics marketed today only colonize the densely populated gut to a limited extent. Bacteriophages comprise the majority of viruses in the human gut virome and there are strong indications that they play important roles in shaping the gut microbiome. Here, we investigate the use of fecal virome transplantation (FVT, sterile filtrated feces) as a mean to alter the gut microbiome composition to lead the way for persistent colonization of two types of probiotics: Lacticaseibacillus rhamnosus GG (LGG) representing a well-established probiotic and Akkermansia muciniphila (AKM) representing a putative next-generation probiotic. Male and female C57BL/6NTac mice were cohoused in pairs from 4 weeks of age and received the following treatment by oral gavage at week 5 and 6: AKM+FVT, LGG+FVT, probiotic sham (Pro-sham)+FVT, LGG+Saline, AKM+Saline, and control (Pro-sham+Saline). The FVT donor material originated from mice with high relative abundance of A. muciniphila. All animals were terminated at age 9 weeks. The FVT treatment did not increase the relative abundance of the administered LGG or AKM in the recipient mice. Instead FVT significantly (p < 0.05) increased the abundance of naturally occurring A. muciniphila compared to the control. This highlights the potential of propagating the existing commensal “probiotics” that have already permanently colonized the gut. Being co-housed male and female, a fraction of the female mice became pregnant. Unexpectedly, the FVT treated mice were found to have a significantly (p < 0.05) higher fertility rate independent of probiotic administration. These preliminary observations urge for follow-up studies investigating interactions between the gut microbiome and fertility.
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spelling pubmed-101678822023-05-10 Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice Rasmussen, Torben Sølbeck Mentzel, Caroline M. Junker Danielsen, Malene Refslund Jakobsen, Rasmus Riemer Zachariassen, Line Sidsel Fisker Castro Mejia, Josue Leonardo Brunse, Anders Hansen, Lars Hestbjerg Hansen, Camilla Hartmann Friis Hansen, Axel Kornerup Nielsen, Dennis Sandris Gut Microbes Research Paper Probiotics are intended to improve gastrointestinal health when consumed. However, the probiotics marketed today only colonize the densely populated gut to a limited extent. Bacteriophages comprise the majority of viruses in the human gut virome and there are strong indications that they play important roles in shaping the gut microbiome. Here, we investigate the use of fecal virome transplantation (FVT, sterile filtrated feces) as a mean to alter the gut microbiome composition to lead the way for persistent colonization of two types of probiotics: Lacticaseibacillus rhamnosus GG (LGG) representing a well-established probiotic and Akkermansia muciniphila (AKM) representing a putative next-generation probiotic. Male and female C57BL/6NTac mice were cohoused in pairs from 4 weeks of age and received the following treatment by oral gavage at week 5 and 6: AKM+FVT, LGG+FVT, probiotic sham (Pro-sham)+FVT, LGG+Saline, AKM+Saline, and control (Pro-sham+Saline). The FVT donor material originated from mice with high relative abundance of A. muciniphila. All animals were terminated at age 9 weeks. The FVT treatment did not increase the relative abundance of the administered LGG or AKM in the recipient mice. Instead FVT significantly (p < 0.05) increased the abundance of naturally occurring A. muciniphila compared to the control. This highlights the potential of propagating the existing commensal “probiotics” that have already permanently colonized the gut. Being co-housed male and female, a fraction of the female mice became pregnant. Unexpectedly, the FVT treated mice were found to have a significantly (p < 0.05) higher fertility rate independent of probiotic administration. These preliminary observations urge for follow-up studies investigating interactions between the gut microbiome and fertility. Taylor & Francis 2023-05-07 /pmc/articles/PMC10167882/ /pubmed/37150906 http://dx.doi.org/10.1080/19490976.2023.2208504 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Rasmussen, Torben Sølbeck
Mentzel, Caroline M. Junker
Danielsen, Malene Refslund
Jakobsen, Rasmus Riemer
Zachariassen, Line Sidsel Fisker
Castro Mejia, Josue Leonardo
Brunse, Anders
Hansen, Lars Hestbjerg
Hansen, Camilla Hartmann Friis
Hansen, Axel Kornerup
Nielsen, Dennis Sandris
Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
title Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
title_full Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
title_fullStr Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
title_full_unstemmed Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
title_short Fecal virome transfer improves proliferation of commensal gut Akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
title_sort fecal virome transfer improves proliferation of commensal gut akkermansia muciniphila and unexpectedly enhances the fertility rate in laboratory mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167882/
https://www.ncbi.nlm.nih.gov/pubmed/37150906
http://dx.doi.org/10.1080/19490976.2023.2208504
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