| Literature DB >> 24629344 |
Subra Kugathasan1, Lee A Denson2, Dirk Gevers3, Yoshiki Vázquez-Baeza4, Will Van Treuren5, Boyu Ren6, Emma Schwager6, Dan Knights7,8, Se Jin Song5, Moran Yassour3, Xochitl C Morgan6, Aleksandar D Kostic3, Chengwei Luo3, Antonio González5, Daniel McDonald5, Yael Haberman2, Thomas Walters9, Susan Baker10, Joel Rosh11, Michael Stephens12, Melvin Heyman13, James Markowitz14, Robert Baldassano15, Anne Griffiths16, Francisco Sylvester17, David Mack18, Sandra Kim19, Wallace Crandall19, Jeffrey Hyams17, Curtis Huttenhower3,6, Rob Knight5,20,21, Ramnik J Xavier3,22,23.
Abstract
Inflammatory bowel diseases (IBDs), including Crohn's disease (CD), are genetically linked to host pathways that implicate an underlying role for aberrant immune responses to intestinal microbiota. However, patterns of gut microbiome dysbiosis in IBD patients are inconsistent among published studies. Using samples from multiple gastrointestinal locations collected prior to treatment in new-onset cases, we studied the microbiome in the largest pediatric CD cohort to date. An axis defined by an increased abundance in bacteria which include Enterobacteriaceae, Pasteurellacaea, Veillonellaceae, and Fusobacteriaceae, and decreased abundance in Erysipelotrichales, Bacteroidales, and Clostridiales, correlates strongly with disease status. Microbiome comparison between CD patients with and without antibiotic exposure indicates that antibiotic use amplifies the microbial dysbiosis associated with CD. Comparing the microbial signatures between the ileum, the rectum, and fecal samples indicates that at this early stage of disease, assessing the rectal mucosal-associated microbiome offers unique potential for convenient and early diagnosis of CD.Entities:
Mesh:
Year: 2014 PMID: 24629344 PMCID: PMC4059512 DOI: 10.1016/j.chom.2014.02.005
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023