Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis
The mouse pathobiont Helicobacter hepaticus can induce typhlocolitis in interleukin-10-deficient mice, and H. hepaticus infection of immunodeficient mice is widely used as a model to study the role of pathogens and commensal bacteria in the pathogenesis of inflammatory bowel disease. C57BL/6J Il10[s...
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Public Library of Science
2013
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Online Access: | http://hdl.handle.net/1721.1/81245 https://orcid.org/0000-0001-9307-6116 |
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author | Yang, Ines Eibach, Daniel Kops, Friederike Brenneke, Birgit Woltemate, Sabrina Schulze, Jessika Bleich, André Gruber, Achim D. Muthupalani, Sureshkumar Fox, James G. Josenhans, Christine Suerbaum, Sebastian |
author2 | Massachusetts Institute of Technology. Department of Biological Engineering |
author_facet | Massachusetts Institute of Technology. Department of Biological Engineering Yang, Ines Eibach, Daniel Kops, Friederike Brenneke, Birgit Woltemate, Sabrina Schulze, Jessika Bleich, André Gruber, Achim D. Muthupalani, Sureshkumar Fox, James G. Josenhans, Christine Suerbaum, Sebastian |
author_sort | Yang, Ines |
collection | MIT |
description | The mouse pathobiont Helicobacter hepaticus can induce typhlocolitis in interleukin-10-deficient mice, and H. hepaticus infection of immunodeficient mice is widely used as a model to study the role of pathogens and commensal bacteria in the pathogenesis of inflammatory bowel disease. C57BL/6J Il10[superscript −/−] mice kept under specific pathogen-free conditions in two different facilities (MHH and MIT), displayed strong differences with respect to their susceptibilities to H. hepaticus-induced intestinal pathology. Mice at MIT developed robust typhlocolitis after infection with H. hepaticus, while mice at MHH developed no significant pathology after infection with the same H. hepaticus strain. We hypothesized that the intestinal microbiota might be responsible for these differences and therefore performed high resolution analysis of the intestinal microbiota composition in uninfected mice from the two facilities by deep sequencing of partial 16S rRNA amplicons. The microbiota composition differed markedly between mice from both facilities. Significant differences were also detected between two groups of MHH mice born in different years. Of the 119 operational taxonomic units (OTUs) that occurred in at least half the cecum or colon samples of at least one mouse group, 24 were only found in MIT mice, and another 13 OTUs could only be found in MHH samples. While most of the MHH-specific OTUs could only be identified to class or family level, the MIT-specific set contained OTUs identified to genus or species level, including the opportunistic pathogen, Bilophila wadsworthia. The susceptibility to H. hepaticus-induced colitis differed considerably between Il10[superscript −/−] mice originating from the two institutions. This was associated with significant differences in microbiota composition, highlighting the importance of characterizing the intestinal microbiome when studying murine models of IBD. |
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institution | Massachusetts Institute of Technology |
language | en_US |
last_indexed | 2024-09-23T12:24:10Z |
publishDate | 2013 |
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spelling | mit-1721.1/812452022-10-01T09:04:43Z Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis Yang, Ines Eibach, Daniel Kops, Friederike Brenneke, Birgit Woltemate, Sabrina Schulze, Jessika Bleich, André Gruber, Achim D. Muthupalani, Sureshkumar Fox, James G. Josenhans, Christine Suerbaum, Sebastian Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Division of Comparative Medicine Muthupalani, Sureshkumar Fox, James G. The mouse pathobiont Helicobacter hepaticus can induce typhlocolitis in interleukin-10-deficient mice, and H. hepaticus infection of immunodeficient mice is widely used as a model to study the role of pathogens and commensal bacteria in the pathogenesis of inflammatory bowel disease. C57BL/6J Il10[superscript −/−] mice kept under specific pathogen-free conditions in two different facilities (MHH and MIT), displayed strong differences with respect to their susceptibilities to H. hepaticus-induced intestinal pathology. Mice at MIT developed robust typhlocolitis after infection with H. hepaticus, while mice at MHH developed no significant pathology after infection with the same H. hepaticus strain. We hypothesized that the intestinal microbiota might be responsible for these differences and therefore performed high resolution analysis of the intestinal microbiota composition in uninfected mice from the two facilities by deep sequencing of partial 16S rRNA amplicons. The microbiota composition differed markedly between mice from both facilities. Significant differences were also detected between two groups of MHH mice born in different years. Of the 119 operational taxonomic units (OTUs) that occurred in at least half the cecum or colon samples of at least one mouse group, 24 were only found in MIT mice, and another 13 OTUs could only be found in MHH samples. While most of the MHH-specific OTUs could only be identified to class or family level, the MIT-specific set contained OTUs identified to genus or species level, including the opportunistic pathogen, Bilophila wadsworthia. The susceptibility to H. hepaticus-induced colitis differed considerably between Il10[superscript −/−] mice originating from the two institutions. This was associated with significant differences in microbiota composition, highlighting the importance of characterizing the intestinal microbiome when studying murine models of IBD. National Institutes of Health (U.S.) (Grant NIH P01-CA26731) National Institutes of Health (U.S.) (Grant NIH P30ES0026731) National Institutes of Health (U.S.) (Grant NIH R01-OD011141) 2013-09-30T16:52:42Z 2013-09-30T16:52:42Z 2013-08 2013-04 Article http://purl.org/eprint/type/JournalArticle 1932-6203 http://hdl.handle.net/1721.1/81245 Yang, Ines, Daniel Eibach, Friederike Kops, Birgit Brenneke, Sabrina Woltemate, Jessika Schulze, André Bleich, et al. “Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis.” Edited by Markus M. Heimesaat. PLoS ONE 8, no. 8 (August 9, 2013): e70783. https://orcid.org/0000-0001-9307-6116 en_US http://dx.doi.org/10.1371/journal.pone.0070783 PLoS ONE Creative Commons Attribution http://creativecommons.org/licenses/by/2.5/ application/pdf Public Library of Science PLoS |
spellingShingle | Yang, Ines Eibach, Daniel Kops, Friederike Brenneke, Birgit Woltemate, Sabrina Schulze, Jessika Bleich, André Gruber, Achim D. Muthupalani, Sureshkumar Fox, James G. Josenhans, Christine Suerbaum, Sebastian Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis |
title | Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis |
title_full | Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis |
title_fullStr | Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis |
title_full_unstemmed | Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis |
title_short | Intestinal Microbiota Composition of Interleukin-10 Deficient C57BL/6J Mice and Susceptibility to Helicobacter hepaticus-Induced Colitis |
title_sort | intestinal microbiota composition of interleukin 10 deficient c57bl 6j mice and susceptibility to helicobacter hepaticus induced colitis |
url | http://hdl.handle.net/1721.1/81245 https://orcid.org/0000-0001-9307-6116 |
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