Commensal Escherichia coli colonization triggers Peyer's patch development
Romana Raphaela GerneriD, Gregory T. WalkeriD, Suzi M. Klaus, Karine MelchioriD, Suzana Hossain, Kareem SiadaiD, Chia-Yun HsuiD, Francisco Javier AlbicoroiD, William SantusiD, Rasika PatkariD, Marvic Carrillo TerrazasiD, Grant J. NortoniD, Flavian TheleniD, Araceli Pérez-LópeziD, Purnima Sharma, Marcus P. WongiD, Victor Lei, Richard M. RansohoffiD, David D. LoiD, Thomas E. LaneiD, Andrea ReboldiiD, Sean‐Paul NuccioiD, Judith BehnseniD, Elina I. ZúñigaiD, Li‐Fan LuiD, , Manuela RaffatelluiD
Abstract
The gut microbiota plays a pivotal role in shaping mucosal immunity, yet the specific microbes contributing to lymphoid tissue development remain poorly defined. Here, we identify Escherichia coli, a pioneer commensal bacterium, as a key driver of naive B cell accumulation in gut Peyers patches and lamina propria via a CXCR2-dependent mechanism. We show that E. coli promotes B cell recruitment through the production of curli amyloid fibers, which signal via Toll-like receptor 2 (TLR2). Notably, this effect extends beyond the neonatal period, revealing a broader temporal window for microbial modulation of mucosal immune development. These findings reveal a previously unrecognized role for a defined gut commensal bacterium and its molecular products in orchestrating the formation of gut-associated lymphoid tissue and B cell recruitment.
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