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Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice
Antibiotic exposure in children has been associated with the risk of Inflammatory Bowel Disease (IBD). Since antibiotic use in children or in their pregnant mother can affect how the intestinal microbiome develops, we asked whether the transfer of an antibiotic-perturbed microbiota from mothers to t...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780248/ https://www.ncbi.nlm.nih.gov/pubmed/29180726 http://dx.doi.org/10.1038/s41564-017-0075-5 |
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author | Schulfer, Anjelique F. Battaglia, Thomas Alvarez, Yelina Bijnens, Luc Ruiz, Victoria E. Ho, Melody Robinson, Serina Ward, Tonya Cox, Laura M. Rogers, Arlin B. Knights, Dan Sartor, R. Balfour Blaser, Martin J. |
author_facet | Schulfer, Anjelique F. Battaglia, Thomas Alvarez, Yelina Bijnens, Luc Ruiz, Victoria E. Ho, Melody Robinson, Serina Ward, Tonya Cox, Laura M. Rogers, Arlin B. Knights, Dan Sartor, R. Balfour Blaser, Martin J. |
author_sort | Schulfer, Anjelique F. |
collection | PubMed |
description | Antibiotic exposure in children has been associated with the risk of Inflammatory Bowel Disease (IBD). Since antibiotic use in children or in their pregnant mother can affect how the intestinal microbiome develops, we asked whether the transfer of an antibiotic-perturbed microbiota from mothers to their children could affect their risk of developing IBD. Here we demonstrate that germ-free adult pregnant mice inoculated with a gut microbial community shaped by antibiotic exposure transmitted their perturbed microbiota to their offspring with high fidelity. Without any direct or continued exposure to antibiotics, this dysbiotic microbiota in the offspring remained distinct from controls for at least 21 weeks. By using both IL-10-deficient and wild type mothers, we showed that both inoculum and genotype shape the microbiota populations in the offspring. Since IL10−/− mice are genetically susceptible to colitis, we could assess the risk due to maternal transmission of an antibiotic-perturbed microbiota. We found that the IL10−/− offspring that had received the perturbed gut microbiota developed markedly increased colitis. Taken together, our findings indicate that antibiotic exposure shaping the maternal gut microbiota has effects that extend to their offspring with both ecological and long-term disease consequences. |
format | Online Article Text |
id | pubmed-5780248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-57802482018-05-27 Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice Schulfer, Anjelique F. Battaglia, Thomas Alvarez, Yelina Bijnens, Luc Ruiz, Victoria E. Ho, Melody Robinson, Serina Ward, Tonya Cox, Laura M. Rogers, Arlin B. Knights, Dan Sartor, R. Balfour Blaser, Martin J. Nat Microbiol Article Antibiotic exposure in children has been associated with the risk of Inflammatory Bowel Disease (IBD). Since antibiotic use in children or in their pregnant mother can affect how the intestinal microbiome develops, we asked whether the transfer of an antibiotic-perturbed microbiota from mothers to their children could affect their risk of developing IBD. Here we demonstrate that germ-free adult pregnant mice inoculated with a gut microbial community shaped by antibiotic exposure transmitted their perturbed microbiota to their offspring with high fidelity. Without any direct or continued exposure to antibiotics, this dysbiotic microbiota in the offspring remained distinct from controls for at least 21 weeks. By using both IL-10-deficient and wild type mothers, we showed that both inoculum and genotype shape the microbiota populations in the offspring. Since IL10−/− mice are genetically susceptible to colitis, we could assess the risk due to maternal transmission of an antibiotic-perturbed microbiota. We found that the IL10−/− offspring that had received the perturbed gut microbiota developed markedly increased colitis. Taken together, our findings indicate that antibiotic exposure shaping the maternal gut microbiota has effects that extend to their offspring with both ecological and long-term disease consequences. 2017-11-27 2018-02 /pmc/articles/PMC5780248/ /pubmed/29180726 http://dx.doi.org/10.1038/s41564-017-0075-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Schulfer, Anjelique F. Battaglia, Thomas Alvarez, Yelina Bijnens, Luc Ruiz, Victoria E. Ho, Melody Robinson, Serina Ward, Tonya Cox, Laura M. Rogers, Arlin B. Knights, Dan Sartor, R. Balfour Blaser, Martin J. Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
title | Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
title_full | Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
title_fullStr | Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
title_full_unstemmed | Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
title_short | Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
title_sort | intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780248/ https://www.ncbi.nlm.nih.gov/pubmed/29180726 http://dx.doi.org/10.1038/s41564-017-0075-5 |
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