MyD88-deficient mice display a profound loss in resistance to Mycobacterium tuberculosis associated with partially impaired Th1 cytokine and nitric oxide synthase 2 expression

Infect Immun. 2004 Apr;72(4):2400-4. doi: 10.1128/IAI.72.4.2400-2404.2004.

Abstract

Mycobacterium tuberculosis possesses agonists for several Toll-like receptors (TLRs), yet mice with single TLR deletions are resistant to acute tuberculosis. MyD88(-/-) mice were used to examine whether TLRs play any role in protection against aerogenic M. tuberculosis H37Rv infection. MyD88(-/-) mice failed to control mycobacterial replication and rapidly succumbed. Moreover, expressions of interleukin 12, tumor necrosis factor alpha, gamma interferon, and nitric oxide synthase 2 were markedly decreased in the knockout animals. These results argue that resistance to M. tuberculosis must depend on MyD88-dependent signals mediated by an as-yet-undetermined TLR or a combination of TLRs.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Antigens, Differentiation / genetics
  • Antigens, Differentiation / physiology*
  • Cytokines / biosynthesis
  • Lung / microbiology
  • Lung / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mycobacterium tuberculosis / immunology*
  • Mycobacterium tuberculosis / pathogenicity
  • Myeloid Differentiation Factor 88
  • Nitric Oxide Synthase / metabolism*
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / physiology*
  • Th1 Cells / immunology
  • Th1 Cells / pathology*
  • Tuberculosis, Pulmonary / immunology*
  • Tuberculosis, Pulmonary / mortality
  • Tuberculosis, Pulmonary / pathology
  • Virulence

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation
  • Cytokines
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Receptors, Immunologic
  • Nitric Oxide Synthase