Host-microbe cross-talk governs amino acid chirality to regulate survival and differentiation of B cells

M. Suzuki, T. Sujino, S. Chiba, Y. Harada, M. Goto, R. Takahashi, M. Mita, K. Hamase, T. Kanai, M. Ito, M. K. Waldor, M. Yasui, J. Sasabe

Research output: Contribution to journalArticlepeer-review

Abstract

Organisms use l-amino acids (l-aa) for most physiological processes. Unlike other organisms, bacteria chiral-convert l-aa to d-configurations as essential components of their cell walls and as signaling molecules in their ecosystems. Mammals recognize microbe-associated molecules to initiate immune responses, but roles of bacterial d-amino acids (d-aa) in mammalian immune systems remain largely unknown. Here, we report that amino acid chirality balanced by bacteria-mammal cross-talk modulates intestinal B cell fate and immunoglobulin A (IgA) production. Bacterial d-aa stimulate M1 macrophages and promote survival of intestinal naïve B cells. Mammalian intestinal d-aa catabolism limits the number of B cells and restricts growth of symbiotic bacteria that activate T cell–dependent IgA class switching of the B cells. Loss of d-aa catabolism results in excessive IgA production and dysbiosis with altered IgA coating on bacteria. Thus, chiral conversion of amino acids is linked to bacterial recognition by mammals to control symbiosis with bacteria.

Original languageEnglish
Article numbereabd6480
JournalScience Advances
Volume7
Issue number10
DOIs
Publication statusPublished - Mar 3 2021

All Science Journal Classification (ASJC) codes

  • General

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