Toll‐Like Receptor 4 Is Not Involved in Host Defense against PulmonaryLegionella pneumophilaInfection in a Mouse Model
Author(s) -
Kamilla D. Lettinga,
Sandrine Florquin,
Peter Speelman,
Ruud van Ketel,
Tom van der Poll,
Annelies Verbon
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/341780
Subject(s) - legionella pneumophila , microbiology and biotechnology , tlr4 , biology , bronchoalveolar lavage , legionnaires' disease , immunology , toll like receptor , pneumonia , legionella , receptor , innate immune system , bacteria , lung , inflammation , immune system , medicine , biochemistry , genetics
Legionella pneumophila is a gram-negative microorganism that causes a severe pneumonia known as "legionnaires disease." Toll-like receptor 4 (TLR4) transduces the lipopolysaccharide signal and is therefore considered to play a role in host defense against gram-negative bacterial infection. To determine the role of TLR4 in L. pneumophila pneumonia, C3H/HeJ mice, which display a nonfunctional gene encoding TLR4 (TLR4), and wild-type (wt) C3H/HeN mice were intranasally inoculated with L. pneumophila serogroup 1. Infection proceeded in an identical way in TLR4 mutant and wt mice, as reflected by similar bacterial outgrowth in the lungs. In addition, the inflammatory responses to L. pneumophila infection-as assessed by histopathologic analysis, cell influx in bronchoalveolar lavage fluid, myeloperoxidase activity in lungs, and lung cytokine concentrations-were indistinguishable in TLR4 mutant and wt mice. These data suggest that, in this mouse model, TLR4 does not play a role in resistance to L. pneumophila.
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