Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 1980 Apr;35:101–106. doi: 10.1289/ehp.8035101

Experimental infection of the respiratory tract with Mycoplasma pneumoniae.

P C Hu, J M Kirtz, D E Gardner, D A Powell
PMCID: PMC1568451  PMID: 6773754

Abstract

M. pneumoniae, a common human respiratory pathogen, has been studied experimentally for years using intranasal inoculation of the golden Syrian hamster. Because of recent evidence outlining the role in pulmonary immune development of particle size and depth of mycoplasma deposition in the hamster lung, we developed an aerosol chamber for the reproducible aerosolization of radiolabeled M. pneumoniae. Organisms were labeled to high specific activity by the incorporation of 3H-oleic acid and aerosolized under airflow and humidity conditions creating a mean particle diameter of 2.0 micrometers. Under these conditions, viable mycoplasmas were reproducibly and evenly distributed to all major lobes of the lung. Examination of radioactive clearance and organism viability within the lung during the first 48 hr after aerosolization have suggested a minimal role for macrophage mycoplasmacidal activity and a more prominent role for ciliary clearance. Data from aerosol infections of hamsters with radio-labeled M. pneumoniae should provide a unique opportunity to examine in a highly controlled manner the effects of air pollutants on the initial stages of infection as well as effects on the development of pulmonary immunity and histologic alterations.

Full text

PDF
101

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Collier A. M., Clyde W. A., Jr, Denny F. W. Biologic effects of Mycoplasma pneumoniae and other mycoplasmas from man on hamster tracheal organ culture. Proc Soc Exp Biol Med. 1969 Dec;132(3):1153–1158. doi: 10.3181/00379727-132-34385. [DOI] [PubMed] [Google Scholar]
  2. Collier A. M., Clyde W. A., Jr, Denny F. W. Mycoplasma pneumoniae in hamster tracheal organ culture: immunofluorescent and electron microscopic studies. Proc Soc Exp Biol Med. 1971 Feb;136(2):569–573. doi: 10.3181/00379727-136-35313. [DOI] [PubMed] [Google Scholar]
  3. DAJANI A. S., CLYDE W. A., Jr, DENNY F. W. EXPERIMENTAL INFECTION WITH MYCOPLASMA PNEUMONIAE (EATON'S AGENT). J Exp Med. 1965 Jun 1;121:1071–1086. doi: 10.1084/jem.121.6.1071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. Foy H. M., Ochs H., Davis S. D., Kenny G. E., Luce R. R. Mycoplasma pneumoniae infections in patients with immunodeficiency syndromes: report of four cases. J Infect Dis. 1973 Apr;127(4):388–393. doi: 10.1093/infdis/127.4.388. [DOI] [PubMed] [Google Scholar]
  6. Green G. M. Integrated defense mechanisms in models of chronic pulmonary disease. Arch Intern Med. 1970 Sep;126(3):500–503. [PubMed] [Google Scholar]
  7. Hu P. C., Collier A. M., Baseman J. B. Alterations in the metabolism of hamster tracheas in organ culture after infection by virulent Mycoplasma pneumoniae. Infect Immun. 1975 Apr;11(4):704–710. doi: 10.1128/iai.11.4.704-710.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hu P. C., Collier A. M., Baseman J. B. Interaction of virulent Mycoplasma pneumoniae with hamster tracheal organ cultures. Infect Immun. 1976 Jul;14(1):217–224. doi: 10.1128/iai.14.1.217-224.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jakab G. J., Green G. M. Regional defense mechanisms of the guinea pig lung. Am Rev Respir Dis. 1973 May;107(5):776–783. doi: 10.1164/arrd.1973.107.5.776. [DOI] [PubMed] [Google Scholar]
  10. Jemski J. V., Hetsko C. M., Helms C. M., Grizzard M. B., Walker J. S., Chanock R. M. Immunoprophylaxis of experimental Mycoplasma pneumoniae disease: effect of aerosol particle size and site of deposition of M. pneumoniae on the pattern of respiratory infection, disease, and immunity in hamsters. Infect Immun. 1977 Apr;16(1):93–98. doi: 10.1128/iai.16.1.93-98.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Jones T. C., Minick R., Yang L. Attachment and ingestion of mycoplasmas by mouse macrophages. II. Scanning electron microscopic observations. Am J Pathol. 1977 May;87(2):347–358. [PMC free article] [PubMed] [Google Scholar]
  12. Muse K. E., Powell D. A., Collier A. M. Mycoplasma pneumoniae in hamster tracheal organ culture studied by scanning electron microscopy. Infect Immun. 1976 Jan;13(1):229–237. doi: 10.1128/iai.13.1.229-237.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Powell D. A., Clyde W. A., Jr Opsonin-reversible resistance of Mycoplasma pneumoniae to in vitro phagocytosis by alveolar macrophages. Infect Immun. 1975 Mar;11(3):540–550. doi: 10.1128/iai.11.3.540-550.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Powell D. A., Muse K. A. Scanning electron microscopy of guinea pig alveolar macrophages: in vitro phagocytosis of Mycoplasma pneumoniae. Lab Invest. 1977 Dec;37(6):535–543. [PubMed] [Google Scholar]
  15. Rylander R. Studies of lung defense to infections in inhalation toxicology. Arch Intern Med. 1970 Sep;126(3):496–499. [PubMed] [Google Scholar]
  16. Shulman S. T., Bartlett J., Clyde W. A., Jr, Ayoub E. M. The unusual severity of Mycoplasmal pneumonia in children with sickle-cell disease. N Engl J Med. 1972 Jul 27;287(4):164–167. doi: 10.1056/NEJM197207272870403. [DOI] [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES