Commensal segmented filamentous bacteria-derived retinoic acid primes host defense to intestinal infection

Author(s):  
Vivienne Woo ◽  
Emily M. Eshleman ◽  
Seika Hashimoto-Hill ◽  
Jordan Whitt ◽  
Shu-en Wu ◽  
...  
1992 ◽  
Vol 5 (6) ◽  
Author(s):  
H. L. B. M. Klaasen ◽  
J. P. Koopman ◽  
F. G. J. Poelma ◽  
M. E. Van Den Brink ◽  
M. H. Bakker ◽  
...  

2012 ◽  
Vol 22 (6) ◽  
pp. 1107-1119 ◽  
Author(s):  
Sünje J. Pamp ◽  
Eoghan D. Harrington ◽  
Stephen R. Quake ◽  
David A. Relman ◽  
Paul C. Blainey

2021 ◽  
Vol 206 (5) ◽  
pp. 941-952
Author(s):  
Nicholas A. Bates ◽  
Anna Li ◽  
Tingting Fan ◽  
Madeline P. Cutcliffe ◽  
Caitlyn B. Dagenet ◽  
...  

2018 ◽  
Vol 9 ◽  
Author(s):  
Grant A. Hedblom ◽  
Holly A. Reiland ◽  
Matthew J. Sylte ◽  
Timothy J. Johnson ◽  
David J. Baumler

2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Hans Jonsson ◽  
Luisa W. Hugerth ◽  
John Sundh ◽  
Eva Lundin ◽  
Anders F. Andersson

AbstractSegmented filamentous bacteria (SFB) are unique immune modulatory bacteria colonizing the small intestine of a variety of animals in a host-specific manner. SFB exhibit filamentous growth and attach to the host’s intestinal epithelium, offering a physical route of interaction. SFB affect functions of the host immune system, among them IgA production and T-cell maturation. Until now, no human-specific SFB genome has been reported. Here, we report the metagenomic reconstruction of an SFB genome from a human ileostomy sample. Phylogenomic analysis clusters the genome with SFB genomes from mouse, rat and turkey, but the genome is genetically distinct, displaying 65–71% average amino acid identity to the others. By screening human faecal metagenomic datasets, we identified individuals carrying sequences identical to the new SFB genome. We thus conclude that a unique SFB variant exists in humans and foresee a renewed interest in the elucidation of SFB functionality in this environment.


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