Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
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
_version_ 1783294702671364096
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
work_keys_str_mv AT schulferanjeliquef intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT battagliathomas intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT alvarezyelina intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT bijnensluc intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT ruizvictoriae intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT homelody intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT robinsonserina intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT wardtonya intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT coxlauram intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT rogersarlinb intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT knightsdan intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT sartorrbalfour intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice
AT blasermartinj intergenerationaltransferofantibioticperturbedmicrobiotaenhancescolitisinsusceptiblemice