Back to Search Start Over

A Connective Tissue Mast-Cell-Specific Receptor Detects Bacterial Quorum-Sensing Molecules and Mediates Antibacterial Immunity

Authors :
Xinzhong Dong
Nadine Serhan
Ying Zhang
Rebecca Yee
Xueqing Wu
Xintong Dong
Priyanka Pundir
Nathachit Limjunyawong
Solomon H. Snyder
Yingzhuan Zhan
Jorge E. Vidal
Chirag Vasavda
Rui Liu
Nicolas Gaudenzio
Johns Hopkins University School of Medicine [Baltimore]
Unité différenciation épidermique et auto-immunité rhumatoïde (UDEAR)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)
Emory University [Atlanta, GA]
Pistre, Karine
Source :
Cell Host & Microbe, Cell Host & Microbe, 2019, 26 (1), pp.114-122.e8. ⟨10.1016/j.chom.2019.06.003⟩, Cell Host Microbe
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

International audience; Quorum sensing molecules (QSMs) are secreted by bacteria to signal population density. Upon reaching a critical concentration, QSMs induce transcriptional alterations in bacteria that enable virulence factor expression and biofilm formation. It is unclear whether mammalian hosts can recognize QSMs to trigger responsive antibacterial immunity. We report that mouse mast cell-specific G protein-coupled-receptor Mrgprb2, and its human homologue MRGPRX2, are receptors for Gram-positive QSMs, including competence-stimulating peptide (CSP)-1. CSP-1 activates Mrgprb2/MRGPRX2, triggering mast cell degranulation which inhibits bacterial growth and prevents biofilm formation. Such antibacterial functions are reduced in Mrgprb2-deficient mast cells, while wildtype mast cells fail to inhibit the growth of bacterial strains lacking CSP-1. Mrgprb2-knockout mice exhibit reduced bacterial clearance, while pharmacologically activating Mrgprb2 in vivo eliminates bacteria and improves disease score. These findings identify a host defense mechanism that uses QSMs as an “Achilles heel” and suggest MRGPRX2 as a potential therapeutic target for controlling bacterial infections.

Details

ISSN :
19313128
Volume :
26
Database :
OpenAIRE
Journal :
Cell Host & Microbe
Accession number :
edsair.doi.dedup.....26179527b1239b175e4e8f585a2faa52
Full Text :
https://doi.org/10.1016/j.chom.2019.06.003