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. 1995 Oct;63(10):4138–4142. doi: 10.1128/iai.63.10.4138-4142.1995

Chronic respiratory mycoplasmosis in C3H/HeN and C57BL/6N mice: lesion severity and antibody response.

S C Cartner 1, J W Simecka 1, J R Lindsey 1, G H Cassell 1, J K Davis 1
PMCID: PMC173581  PMID: 7558330

Abstract

Mycoplasma pneumoniae is a leading, worldwide cause of death and disability due to pneumonia. Mycoplasma pulmonis infection in mice is an invaluable model for the study of host defenses against respiratory mycoplasmas in vivo. C3H/HeN mice are much more susceptible to acute inflammatory lung disease due to M. pulmonis than C57BL/6N mice, but little is known about the chronic disease in these mouse strains. We infected C3H/HeN and C57BL/6N mice with 10(4) CFU of M. pulmonis UAB CT and evaluated them at weekly intervals by quantitative mycoplasma culture of nasal passages, trachea, and lungs, assessment of lesion severity in nasal passages, trachea, and lungs, and determination of serum immunoglobulin classes and subclasses by enzyme-linked immunosorbent assay. We found that C3H/HeN mice had 2 to 5 logs more organisms in their lungs and far more severe lung disease than C57BL/6N mice through 63 days postinfection. Although both strains of mice developed the same classes of antibody, C3H/HeN mice had much greater anti-M. pulmonis immunoglobulin G (IgG) responses in the IgG1 and IgG2a subclasses than C57BL/6N mice. These results suggest that adaptive immunity does not effect resolution of chronic mycoplasma infection and disease in the lungs.

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Selected References

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  1. Cassell G. H. Derrick Edward Award Lecture. The pathogenic potential of mycoplasmas: Mycoplasma pulmonis as a model. Rev Infect Dis. 1982 May-Jun;4 (Suppl):S18–S34. doi: 10.1093/clinids/4.supplement_1.s18. [DOI] [PubMed] [Google Scholar]
  2. Cassell G. H., Lindsey J. R., Baker H. J. Immune response of pathogen-free mice inoculated intranasally with Mycoplasma pulmonis. J Immunol. 1974 Jan;112(1):124–136. [PubMed] [Google Scholar]
  3. Davidson M. K., Lindsey J. R., Parker R. F., Tully J. G., Cassell G. H. Differences in virulence for mice among strains of Mycoplasma pulmonis. Infect Immun. 1988 Aug;56(8):2156–2162. doi: 10.1128/iai.56.8.2156-2162.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Davis J. K., Cassell G. H. Murine respiratory mycoplasmosis in LEW and F344 rats: strain differences in lesion severity. Vet Pathol. 1982 May;19(3):280–293. doi: 10.1177/030098588201900306. [DOI] [PubMed] [Google Scholar]
  5. Davis J. K., Delozier K. M., Asa D. K., Minion F. C., Cassell G. H. Interactions between murine alveolar macrophages and Mycoplasma pulmonis in vitro. Infect Immun. 1980 Aug;29(2):590–599. doi: 10.1128/iai.29.2.590-599.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Davis J. K., Parker R. F., White H., Dziedzic D., Taylor G., Davidson M. K., Cox N. R., Cassell G. H. Strain differences in susceptibility to murine respiratory mycoplasmosis in C57BL/6 and C3H/HeN mice. Infect Immun. 1985 Dec;50(3):647–654. doi: 10.1128/iai.50.3.647-654.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Davis J. K., Thorp R. B., Parker R. F., White H., Dziedzic D., D'Arcy J., Cassell G. H. Development of an aerosol model of murine respiratory mycoplasmosis in mice. Infect Immun. 1986 Oct;54(1):194–201. doi: 10.1128/iai.54.1.194-201.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Denny F. W., Clyde W. A., Jr, Glezen W. P. Mycoplasma pneumoniae disease: clinical spectrum, pathophysiology, epidemiology, and control. J Infect Dis. 1971 Jan;123(1):74–92. doi: 10.1093/infdis/123.1.74. [DOI] [PubMed] [Google Scholar]
  9. Denny F. W., Taylor-Robinson D., Allison A. C. The role of thymus-dependent immunity in Mycoplasma pulmonis infections of mice. J Med Microbiol. 1972 Aug;5(3):327–336. doi: 10.1099/00222615-5-3-327. [DOI] [PubMed] [Google Scholar]
  10. Faulkner C. B., Simecka J. W., Davidson M. K., Davis J. K., Schoeb T. R., Lindsey J. R., Everson M. P. Gene expression and production of tumor necrosis factor alpha, interleukin 1, interleukin 6, and gamma interferon in C3H/HeN and C57BL/6N mice in acute Mycoplasma pulmonis disease. Infect Immun. 1995 Oct;63(10):4084–4090. doi: 10.1128/iai.63.10.4084-4090.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Fernald G. W., Collier A. M., Clyde W. A., Jr Respiratory infections due to Mycoplasma pneumoniae in infants and children. Pediatrics. 1975 Mar;55(3):327–335. [PubMed] [Google Scholar]
  12. Flournoy D. J., Jones J. B., 3rd The significance of infection as a cause of death in veterans. Mil Med. 1987 Nov;152(11):587–589. [PubMed] [Google Scholar]
  13. Foy H. M., Kenny G. E., Cooney M. K., Allan I. D. Long-term epidemiology of infections with Mycoplasma pneumoniae. J Infect Dis. 1979 Jun;139(6):681–687. doi: 10.1093/infdis/139.6.681. [DOI] [PubMed] [Google Scholar]
  14. Horowitz S. A., Cassell G. H. Detection of antibodies to Mycoplasma pulmonis by an enzyme-linked immunosorbent assay. Infect Immun. 1978 Oct;22(1):161–170. doi: 10.1128/iai.22.1.161-170.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lai W. C., Linton G., Bennett M., Pakes S. P. Genetic control of resistance to Mycoplasma pulmonis infection in mice. Infect Immun. 1993 Nov;61(11):4615–4621. doi: 10.1128/iai.61.11.4615-4621.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lindsey J. R., Baker H. J., Overcash R. G., Cassell G. H., Hunt C. E. Murine chronic respiratory disease. Significance as a research complication and experimental production with Mycoplasma pulmonis. Am J Pathol. 1971 Sep;64(3):675–708. [PMC free article] [PubMed] [Google Scholar]
  17. Mosmann T. R., Coffman R. L. TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu Rev Immunol. 1989;7:145–173. doi: 10.1146/annurev.iy.07.040189.001045. [DOI] [PubMed] [Google Scholar]
  18. Müller I., Pedrazzini T., Farrell J. P., Louis J. T-cell responses and immunity to experimental infection with leishmania major. Annu Rev Immunol. 1989;7:561–578. doi: 10.1146/annurev.iy.07.040189.003021. [DOI] [PubMed] [Google Scholar]
  19. Parker R. F., Davis J. K., Blalock D. K., Thorp R. B., Simecka J. W., Cassell G. H. Pulmonary clearance of Mycoplasma pulmonis in C57BL/6N and C3H/HeN mice. Infect Immun. 1987 Nov;55(11):2631–2635. doi: 10.1128/iai.55.11.2631-2635.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Parker R. F., Davis J. K., Cassell G. H., White H., Dziedzic D., Blalock D. K., Thorp R. B., Simecka J. W. Short-term exposure to nitrogen dioxide enhances susceptibility to murine respiratory mycoplasmosis and decreases intrapulmonary killing of Mycoplasma pulmonis. Am Rev Respir Dis. 1989 Aug;140(2):502–512. doi: 10.1164/ajrccm/140.2.502. [DOI] [PubMed] [Google Scholar]
  21. Pinson D. M., Schoeb T. R., Lindsey J. R., Davis J. K. Evaluation by scoring and computerized morphometry of lesions of early Mycoplasma pulmonis infection and ammonia exposure in F344/N rats. Vet Pathol. 1986 Sep;23(5):550–555. doi: 10.1177/030098588602300502. [DOI] [PubMed] [Google Scholar]
  22. Rose F. V., Cebra J. J. Isotype commitment of B cells and dissemination of the primed state after mucosal stimulation with Mycoplasma pulmonis. Infect Immun. 1985 Aug;49(2):428–434. doi: 10.1128/iai.49.2.428-434.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Rose F. V., Cebra J. J. Secondary intratracheal infection of mice with Mycoplasma pulmonis generates IgG1 memory B cells. Isr J Med Sci. 1987 May;23(5):490–495. [PubMed] [Google Scholar]
  24. Simecka J. W., Cassell G. H. Serum antibody and cellular responses in LEW and F344 rats after immunization with Mycoplasma pulmonis antigens. Infect Immun. 1987 Mar;55(3):731–735. doi: 10.1128/iai.55.3.731-735.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Simecka J. W., Davis J. K., Cassell G. H. Serum antibody does not account for differences in the severity of chronic respiratory disease caused by Mycoplasma pulmonis in LEW and F344 rats. Infect Immun. 1989 Nov;57(11):3570–3575. doi: 10.1128/iai.57.11.3570-3575.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Taylor G., Howard C. J. Protection of mice against Mycoplasma pulmonis infection using purified mouse immunoglobulins: comparison between protective effect and biological properties of immunoglobulin classes. Immunology. 1981 Jul;43(3):519–525. [PMC free article] [PubMed] [Google Scholar]
  27. Taylor G., Taylor-Robinson D. Effects of active and passive immunization on Mycoplasma pulmonis-induced pneumonia in mice. Immunology. 1976 May;30(5):611–618. [PMC free article] [PubMed] [Google Scholar]

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