A Novel Polymorphism in the Toll-Like Receptor 2 Gene and Its Potential Association with Staphylococcal Infection

Author:

Lorenz Eva12,Mira Jean Paul3,Cornish Kristyn L.1,Arbour Nancy C.1,Schwartz David A.12

Affiliation:

1. Department of Medicine1 and

2. Department of Veterans Affairs Medical Center,2

3. The University of Iowa, Iowa City, Iowa, and the Medical Intensive Care Unit, Cochin University Hospital, Paris, France3

Abstract

ABSTRACT The toll-like receptor 2 (TLR2) has gained importance as a major mammalian receptor for lipoproteins derived from the cell wall of a variety of bacteria, such as Borrelia burgdorferi , Treponema pallidum , and Mycoplasma fermentans . We were interested in identifying mutations in the TLR2 gene that might prove to be associated with altered susceptibility to septic shock. We performed a mutation screen of the TLR2 gene using single-stranded conformational polymorphism in 110 normal, healthy study subjects and detected an Arg753Gln mutation in three individuals. No other missense mutations were detected in the TLR2 open reading frame. Functional studies demonstrate that the Arg753Gln polymorphism, in comparison to the wild-type TLR2 gene, is significantly less responsive to bacterial peptides derived from B. burgdorferi and T. pallidum . In a septic shock population, the Arg753Gln TLR2 polymorphism occurred in 2 out of 91 septic patients. More importantly, both of the subjects with the TLR2 Arg753Gln polymorphism had staphylococcal infections. These findings suggest that a mutation in the TLR2 gene may predispose individuals to life-threatening bacterial infections.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference17 articles.

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4. Human toll-like receptor 2 mediates monocyte activation by Listeria monocytogenes, but not by group B streptococci or lipopolysaccharide;Flo T.;J. Immunol.,2000

5. Cutting edge: cells that carry a null allele for toll-like receptor 2 are capable of responding to endotoxin;Heine H.;J. Immunol.,1999

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