| Literature DB >> 30763538 |
Lasha Gogokhia1, Kate Buhrke2, Rickesha Bell2, Brenden Hoffman2, D Garrett Brown2, Christin Hanke-Gogokhia2, Nadim J Ajami3, Matthew C Wong3, Arevik Ghazaryan2, John F Valentine4, Nathan Porter5, Eric Martens5, Ryan O'Connell2, Vinita Jacob6, Ellen Scherl6, Carl Crawford6, W Zac Stephens2, Sherwood R Casjens2, Randy S Longman6, June L Round7.
Abstract
Bacteriophages are the most abundant members of the microbiota and have the potential to shape gut bacterial communities. Changes to bacteriophage composition are associated with disease, but how phages impact mammalian health remains unclear. We noted an induction of host immunity when experimentally treating bacterially driven cancer, leading us to test whether bacteriophages alter immune responses. Treating germ-free mice with bacteriophages leads to immune cell expansion in the gut. Lactobacillus, Escherichia, and Bacteroides bacteriophages and phage DNA stimulated IFN-γ via the nucleotide-sensing receptor TLR9. The resultant immune responses were both phage and bacteria specific. Additionally, increasing bacteriophage levels exacerbated colitis via TLR9 and IFN-γ. Similarly, ulcerative colitis (UC) patients responsive to fecal microbiota transplantation (FMT) have reduced phages compared to non-responders, and mucosal IFN-γ positively correlates with bacteriophage levels. Bacteriophages from active UC patients induced more IFN-γ compared to healthy individuals. Collectively, these results indicate that bacteriophages can alter mucosal immunity to impact mammalian health. Published by Elsevier Inc.Entities:
Keywords: FMT; IFN-y; T cells; TLR9; Th1; bacteriophages; colitis; dendritic cells
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Year: 2019 PMID: 30763538 PMCID: PMC6885004 DOI: 10.1016/j.chom.2019.01.008
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023