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Mycobacterial Infection in TLR2 and TLR6 Knockout Mice
Author(s) -
Sugawara Isamu,
Yamada Hiroyuki,
Li Chuanyou,
Mizuno Satoru,
Takeuchi Osamu,
Akira Shizuo
Publication year - 2003
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.2003.tb03404.x
Subject(s) - tlr2 , biology , knockout mouse , pathogenesis , nitric oxide synthase , immunology , mycobacterium tuberculosis , cytokine , interleukin 17 , tuberculosis , microbiology and biotechnology , inflammation , nitric oxide , pathology , endocrinology , receptor , medicine , tlr4 , biochemistry
To investigate the role of TLR in the development of murine tuberculosis in vivo , TLR2 and TLR6 knockout (KO) mice were infected with Mycobacterium tuberculosis by placing them in the exposure chamber of an airborne infection apparatus. Both TLR2 and TLR6 KO mice survived until sacrifice at 12 weeks after infection. Infected TLR2 KO mice developed granulomatous pulmonary lesions with neutrophil infiltration, which were slightly larger in size than those in wild‐type mice. Pulmonary levels of the mRNAs for inducible nitric oxide synthase (iNOS), TNF‐α, TGF‐β, IL‐1β, and IL‐2 were significantly lower, but levels of the mRNAs for IL‐4 and IL‐6 were higher, than in wild‐type (WT) mice. No significant difference was recognized in cytokine mRNA expression between TLR2 KO and WT mice at 12 weeks after infection. DNA binding by NF‐κB was low in TLR2 KO mice. On the other hand, TLR6 KO mice were not different from WT mice in terms of pulmonary histopathology, mRNA expression and CFU assay. Therefore, TLR2 does not play an essential role in the pathogenesis of murine tuberculosis, although it is important for defense against mycobacterial infection.