Imperial College London

DrThomasClarke

Faculty of MedicineDepartment of Medicine

Research Fellow
 
 
 
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Contact

 

+44 (0)20 7594 2074thomas.clarke

 
 
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Location

 

5.40CFlowers buildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Clarke:2010:10.1038/nm.2087,
author = {Clarke, TB and Davis, KM and Lysenko, ES and Zhou, AY and Yu, Y and Weiser, JN},
doi = {10.1038/nm.2087},
journal = {Nat Med},
pages = {228--231},
title = {Recognition of peptidoglycan from the microbiota by Nod1 enhances systemic innate immunity.},
url = {http://dx.doi.org/10.1038/nm.2087},
volume = {16},
year = {2010}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Humans are colonized by a large and diverse bacterial flora (the microbiota) essential for the development of the gut immune system. A broader role for the microbiota as a major modulator of systemic immunity has been proposed; however, evidence and a mechanism for this role have remained elusive. We show that the microbiota are a source of peptidoglycan that systemically primes the innate immune system, enhancing killing by bone marrow-derived neutrophils of two major pathogens: Streptococcus pneumoniae and Staphylococcus aureus. This requires signaling via the pattern recognition receptor nucleotide-binding, oligomerization domain-containing protein-1 (Nod1, which recognizes meso-diaminopimelic acid (mesoDAP)-containing peptidoglycan found predominantly in Gram-negative bacteria), but not Nod2 (which detects peptidoglycan found in Gram-positive and Gram-negative bacteria) or Toll-like receptor 4 (Tlr4, which recognizes lipopolysaccharide). We show translocation of peptidoglycan from the gut to neutrophils in the bone marrow and show that peptidoglycan concentrations in sera correlate with neutrophil function. In vivo administration of Nod1 ligands is sufficient to restore neutrophil function after microbiota depletion. Nod1(-/-) mice are more susceptible than wild-type mice to early pneumococcal sepsis, demonstrating a role for Nod1 in priming innate defenses facilitating a rapid response to infection. These data establish a mechanism for systemic immunomodulation by the microbiota and highlight potential adverse consequences of microbiota disruption by broad-spectrum antibiotics on innate immune defense to infection.
AU - Clarke,TB
AU - Davis,KM
AU - Lysenko,ES
AU - Zhou,AY
AU - Yu,Y
AU - Weiser,JN
DO - 10.1038/nm.2087
EP - 231
PY - 2010///
SP - 228
TI - Recognition of peptidoglycan from the microbiota by Nod1 enhances systemic innate immunity.
T2 - Nat Med
UR - http://dx.doi.org/10.1038/nm.2087
UR - https://www.ncbi.nlm.nih.gov/pubmed/20081863
VL - 16
ER -