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Impact of antibiotic perturbation on fecal viral communities in mice

Viruses and bacteriophages have a strong impact on intestinal barrier function and the composition and functional properties of commensal bacterial communities. Shifts of the fecal virome might be involved in human diseases, including inflammatory bowel disease (IBD). Loss-of-function variants in th...

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Autores principales: Moltzau Anderson, Jacqueline, Lachnit, Tim, Lipinski, Simone, Falk-Paulsen, Maren, Rosenstiel, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836353/
https://www.ncbi.nlm.nih.gov/pubmed/36413074
http://dx.doi.org/10.1093/g3journal/jkac293
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author Moltzau Anderson, Jacqueline
Lachnit, Tim
Lipinski, Simone
Falk-Paulsen, Maren
Rosenstiel, Philip
author_facet Moltzau Anderson, Jacqueline
Lachnit, Tim
Lipinski, Simone
Falk-Paulsen, Maren
Rosenstiel, Philip
author_sort Moltzau Anderson, Jacqueline
collection PubMed
description Viruses and bacteriophages have a strong impact on intestinal barrier function and the composition and functional properties of commensal bacterial communities. Shifts of the fecal virome might be involved in human diseases, including inflammatory bowel disease (IBD). Loss-of-function variants in the nucleotide-binding oligomerization domain-containing protein 2 (NOD2) gene are associated with an increased risk of developing Crohn’s disease, a subtype of human chronic IBD, where specific changes in fecal viral communities have also been described. To improve our understanding of the dynamics of the enteric virome, we longitudinally characterized the virome in fecal samples from wild-type C57BL/6J and NOD2 knock-out mice in response to an antibiotic perturbation. Sequencing of virus-like particles demonstrated both a high diversity and high interindividual variation of the murine fecal virome composed of eukaryotic viruses and bacteriophages. Antibiotics had a significant impact on the fecal murine virome. Viral community composition only partially recovered in the observation period (10 weeks after cessation of antibiotics) irrespective of genotype. However, compositional shifts in the virome and bacteriome were highly correlated, suggesting that the loss of specific phages may contribute to prolonged dysregulation of the bacterial community composition. We suggest that therapeutic interference with the fecal virome may represent a novel approach in microbiota-targeted therapies.
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spelling pubmed-98363532023-01-17 Impact of antibiotic perturbation on fecal viral communities in mice Moltzau Anderson, Jacqueline Lachnit, Tim Lipinski, Simone Falk-Paulsen, Maren Rosenstiel, Philip G3 (Bethesda) Investigation Viruses and bacteriophages have a strong impact on intestinal barrier function and the composition and functional properties of commensal bacterial communities. Shifts of the fecal virome might be involved in human diseases, including inflammatory bowel disease (IBD). Loss-of-function variants in the nucleotide-binding oligomerization domain-containing protein 2 (NOD2) gene are associated with an increased risk of developing Crohn’s disease, a subtype of human chronic IBD, where specific changes in fecal viral communities have also been described. To improve our understanding of the dynamics of the enteric virome, we longitudinally characterized the virome in fecal samples from wild-type C57BL/6J and NOD2 knock-out mice in response to an antibiotic perturbation. Sequencing of virus-like particles demonstrated both a high diversity and high interindividual variation of the murine fecal virome composed of eukaryotic viruses and bacteriophages. Antibiotics had a significant impact on the fecal murine virome. Viral community composition only partially recovered in the observation period (10 weeks after cessation of antibiotics) irrespective of genotype. However, compositional shifts in the virome and bacteriome were highly correlated, suggesting that the loss of specific phages may contribute to prolonged dysregulation of the bacterial community composition. We suggest that therapeutic interference with the fecal virome may represent a novel approach in microbiota-targeted therapies. Oxford University Press 2022-11-22 /pmc/articles/PMC9836353/ /pubmed/36413074 http://dx.doi.org/10.1093/g3journal/jkac293 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Moltzau Anderson, Jacqueline
Lachnit, Tim
Lipinski, Simone
Falk-Paulsen, Maren
Rosenstiel, Philip
Impact of antibiotic perturbation on fecal viral communities in mice
title Impact of antibiotic perturbation on fecal viral communities in mice
title_full Impact of antibiotic perturbation on fecal viral communities in mice
title_fullStr Impact of antibiotic perturbation on fecal viral communities in mice
title_full_unstemmed Impact of antibiotic perturbation on fecal viral communities in mice
title_short Impact of antibiotic perturbation on fecal viral communities in mice
title_sort impact of antibiotic perturbation on fecal viral communities in mice
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836353/
https://www.ncbi.nlm.nih.gov/pubmed/36413074
http://dx.doi.org/10.1093/g3journal/jkac293
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