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dc.contributor.authorGe, Zhongming
dc.contributor.authorSheh, Alexander
dc.contributor.authorFeng, Yan
dc.contributor.authorMuthupalani, Sureshkumar
dc.contributor.authorGe, Lili
dc.contributor.authorWang, Chuanwu
dc.contributor.authorKurnick, Susanna
dc.contributor.authorMannion, Anthony
dc.contributor.authorWhary, Mark T
dc.contributor.authorFox, James G
dc.date.accessioned2018-09-06T19:34:34Z
dc.date.available2018-09-06T19:34:34Z
dc.date.issued2018-05
dc.date.submitted2017-11
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/1721.1/117659
dc.description.abstractC57BL/6 (B6) mice from Taconic Sciences (Tac) and the Jackson Laboratory (Jax) were infected with H. pylori PMSS1 (Hp) for 16 week; there was no significant difference in the gastric histologic activity index between Hp infected Tac and Jax B6. However, the degree of gastric mucous metaplasia and Th1-associated IgG2c levels in response to Hp infection were increased in Tac mice over Jax mice, whereas the colonization levels of gastric Hp were higher by 8-fold in Jax B6 compared with Tac B6. Additionally, mRNA expression of gastric Il-1β, Il-17A and RegIIIγ were significantly lower in the infected Tac compared to the infected Jax mice. There were significant differences in the microbial community structures in stomach, colon, and feces between Jax and Tac B6 females. Differences in gastric microbial communities between Jax and Tac B6 females are predicted to affect the metagenome. Moreover, Hp infection perturbed the microbial community structures in the stomach, colon and feces of Jax mice, but only altered the colonic microbial composition of Tac mice. Our data indicate that the GI microbiome of Tac B6 mice is compositionally distinct from Jax B6 mice, which likely resulted in different pathological, immunological, and microbial responses to Hp infection.en_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41598-018-25927-2en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleHelicobacter pylori-infected C57BL/6 mice with different gastrointestinal microbiota have contrasting gastric pathology, microbial and host immune responsesen_US
dc.typeArticleen_US
dc.identifier.citationGe, Zhongming et al. “Helicobacter Pylori-Infected C57BL/6 Mice with Different Gastrointestinal Microbiota Have Contrasting Gastric Pathology, Microbial and Host Immune Responses.” Scientific Reports 8, 1 (May 2018): 8014 © 2018 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.mitauthorGe, Zhongming
dc.contributor.mitauthorSheh, Alexander
dc.contributor.mitauthorFeng, Yan
dc.contributor.mitauthorMuthupalani, Sureshkumar
dc.contributor.mitauthorGe, Lili
dc.contributor.mitauthorWang, Chuanwu
dc.contributor.mitauthorKurnick, Susanna
dc.contributor.mitauthorMannion, Anthony
dc.contributor.mitauthorWhary, Mark T
dc.contributor.mitauthorFox, James G
dc.relation.journalScientific Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-08-29T18:25:40Z
dspace.orderedauthorsGe, Zhongming; Sheh, Alexander; Feng, Yan; Muthupalani, Sureshkumar; Ge, Lili; Wang, Chuanwu; Kurnick, Susanna; Mannion, Anthony; Whary, Mark T.; Fox, James G.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9850-161X
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
mit.licensePUBLISHER_CCen_US


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