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Published on: April 2, 2014
Resistance to Mycoplasma pulmonis mediated by activated natural killer cells
W C Lai1, M Bennett, S P Pakes
1Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235.
Abstract:
Infection of C57BL/6J mice with Mycoplasma pulmonis (MP) enhanced NK cell function 3-7 days later, as detected by in vitro and in vivo assays. Moreover, spleen and lung cells of acutely infected C57BL/6J mice inhibited MP growth in vitro. The effectors were eliminated by treatment with anti-NK antibody in vivo and anti-asialo GM1 serum or anti-3A4 antibody plus complement in vitro. Clearance of viable and radiolabeled MP from the lungs was also enhanced in acutely infected mice. Acutely infected mice with severe combined immunodeficiency (SCID) eliminated viable MP faster than did uninfected mice. Antibodies to interferon-gamma (IFN-gamma) impaired clearance of MP from the lungs of SCID mice and decreased their survival times. Activated NK cells can function in resistance to early stages of infection with MP. NK cells directly inhibit MP with secrete IFN-gamma, which may activate macrophages or inhibit the growth of MP or both.
Insights
Natural killer (NK) cells enhance resistance to Mycoplasma pulmonis (MP) infection in mice. Activated NK cells directly inhibit MP growth and improve pathogen clearance, highlighting their role in early-stage immunity.
Area of Science:
- Immunology
- Microbiology
- Infectious Diseases
Background:
- Mycoplasma pulmonis (MP) is a common respiratory pathogen.
- The role of innate immunity, particularly NK cells, in early MP infection is not fully understood.
Purpose of the Study:
- To investigate the role of NK cells in the host response to Mycoplasma pulmonis infection in C57BL/6J mice.
Main Methods:
- Infection of C57BL/6J mice with MP.
- In vitro and in vivo assays to measure NK cell function.
- Depletion of NK cells using specific antibodies.
- Assessment of MP clearance in SCID mice with and without IFN-gamma blockade.
Main Results:
- MP infection enhanced NK cell activity 3-7 days post-infection.
- Spleen and lung cells from infected mice inhibited MP growth in vitro.
- NK cell depletion abrogated the protective effect.
- Enhanced MP clearance was observed in infected mice, including SCID mice.
- IFN-gamma blockade impaired MP clearance and reduced survival in SCID mice.
Conclusions:
- Activated NK cells contribute to early resistance against Mycoplasma pulmonis.
- NK cells directly inhibit MP growth and may secrete IFN-gamma to activate macrophages or inhibit MP.
- NK cells are crucial components of the innate immune response to early MP infection.
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