| Literature DB >> 24637807 |
Julie Mirpuri1, Megan Raetz2, Carolyn R Sturge2, Cara L Wilhelm2, Alicia Benson2, Rashmin C Savani1, Lora V Hooper3, Felix Yarovinsky2.
Abstract
The intestinal microbiota changes dynamically from birth to adulthood. In this study we identified γ-Proteobacteria as a dominant phylum present in newborn mice that is suppressed in normal adult microbiota. The transition from a neonatal to a mature microbiota was in part regulated by induction of a γ-Proteobacteria-specific IgA response. Neocolonization experiments in germ-free mice further revealed a dominant Proteobacteria-specific IgA response triggered by the immature microbiota. Finally, a role for B cells in the regulation of microbiota maturation was confirmed in IgA-deficient mice. Mice lacking IgA had persistent intestinal colonization with γ-Proteobacteria that resulted in sustained intestinal inflammation and increased susceptibility to neonatal and adult models of intestinal injury. Collectively, these results identify an IgA-dependent mechanism responsible for the maturation of the intestinal microbiota.Entities:
Keywords: IgA; colitis; microbiota; necrotizing enterocolitis; proteobacteria
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Year: 2013 PMID: 24637807 PMCID: PMC4049932 DOI: 10.4161/gmic.26489
Source DB: PubMed Journal: Gut Microbes ISSN: 1949-0976