Abstract
Pneumonia caused by Mycoplasma pulmonis and Pasteurella pneumotropica was studied in conventional, specific pathogen-free (SPF), and germ-free mice. When P. pneumotropica was serially passed in conventional mice, M. pulmonis, as well as P. pneumotropica, was recovered from mice with gross lesions. When M. pulmonis was serially passed in conventional mice, both organisms were recovered. SPF mice given a nasal instillation of M. pulmonis alone, P. pneumotropica alone, or a combination of the two developed pneumonia when both organisms were present. These findings suggested that both organisms contribute to typical murine pneumonia. That M. pulmonis might be an L form of P. pneumotropica was suggested because some SPF mice inoculated with either organism yielded both on culture. This possibility was investigated with mole per cent guanine plus cytosine (GC) content and nucleic acid hybridization techniques. The GC content of P. pneumotropica is 42.2 mole per cent and that of M. pulmonis is 28.6 mole per cent. No specific hybrids between deoxyribonucleic acid (DNA) from M. pulmonis and DNA from P. pneumotropica were detected. This and the wide disparity in GC content showed that M. pulmonis is not an L form of P. pneumotropica. In germ-free mice, intranasal instillation with either organism alone produced pneumonia. The lesions produced when each organism was inoculated independently were characterized by areas of consolidation with perivascular and peribronchial lymphocytic infiltration. Qualitatively, the lesions produced when both organisms were inoculated simultaneously more closely resembled those seen in naturally occurring murine pneumonia. Statistical analysis indicated that the quantitative effect of the two organisms was additive. The indirect fluorescent antibody technique was used to locate organisms in lung tissue sections. M. pulmonis localized in the bronchial epithelium and P. pneumotropica localized in the alveolar lesions.
Full text
PDF












Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adler H. E. Mycoplasmosis in animals. Adv Vet Sci. 1965;10:205–244. [PubMed] [Google Scholar]
- Bauer H., Paronetto F., Burns W. A., Einheber A. The enhancing effect of the microbial flora on macrophage function and the immune response. A study in germfree mice. J Exp Med. 1966 Jun 1;123(6):1013–1024. doi: 10.1084/jem.123.6.1013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brennan P. C., Fritz T. E., Flynn R. J. Pasteurella pneumotropica: cultural and biochemical characteristics, and its association with disease in laboratory animals. Lab Anim Care. 1965 Oct;15(5):307–312. [PubMed] [Google Scholar]
- CLYDE W. A., Jr MYCOPLASMA SPECIES IDENTIFICATION BASED UPON GROWTH INHIBITION BY SPECIFIC ANTISERA. J Immunol. 1964 Jun;92:958–965. [PubMed] [Google Scholar]
- 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]
- Denhardt D. T. A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun. 1966 Jun 13;23(5):641–646. doi: 10.1016/0006-291x(66)90447-5. [DOI] [PubMed] [Google Scholar]
- GRAY D. F., CAMPBELL A. L. The use of chloramphenicol and foster mothers in the control of natural pasteurellosis in experimental mice. Aust J Exp Biol Med Sci. 1953 Apr;31(2):161–165. doi: 10.1038/icb.1953.19. [DOI] [PubMed] [Google Scholar]
- GROSS W. B. Symposium on chronic respiratory diseases of poultry. II. The role of Escherichia coli in the cause of chronic respiratory disease and certain other respiratory diseases. Am J Vet Res. 1958 Apr;19(71):448–452. [PubMed] [Google Scholar]
- HEYL J. G. A study of Pasteurella strains from animal sources. Antonie Van Leeuwenhoek. 1963;29:79–83. doi: 10.1007/BF02046040. [DOI] [PubMed] [Google Scholar]
- HOAG W. G., WETMORE P. W., ROGERS J., MEIER H. A study of latent Pasteurella infection in a mouse colony. J Infect Dis. 1962 Sep-Oct;111:135–140. doi: 10.1093/infdis/111.2.135. [DOI] [PubMed] [Google Scholar]
- HOWELL E. V., WARD J. R., JONES R. S. Mycoplasmal (PPLO) polyarthritis and tumor regression in rats. Proc Soc Exp Biol Med. 1959 Oct;102:210–212. doi: 10.3181/00379727-102-25195. [DOI] [PubMed] [Google Scholar]
- IBANEZ M. L., RUSSELL W. O., CHANG J. P., SPEECE A. J. Cold chamber frozen sections for operating room diagnosis and routine surgical pathology. Lab Invest. 1960 Jan-Feb;9:98–109. [PubMed] [Google Scholar]
- JAWETZ E. A pneumotropic pasteurella of laboratory animals; bacteriological and serological characteristics of the organism. J Infect Dis. 1950 Mar-Apr;86(2):172–183. doi: 10.1093/infdis/86.2.172. [DOI] [PubMed] [Google Scholar]
- JAWETZ E., BAKER W. H. A pneumotropic pasteurella of laboratory animals; pathological and immunological studies with the organism. J Infect Dis. 1950 Mar-Apr;86(2):184–196. doi: 10.1093/infdis/86.2.184. [DOI] [PubMed] [Google Scholar]
- LIU C. Studies on primary atypical pneumonia. I. Localization, isolation, and cultivation of a virus in chick embryos. J Exp Med. 1957 Oct 1;106(4):455–466. doi: 10.1084/jem.106.4.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lutsky I. I., Organick A. B. Pneumonia due to mycoplasma in gnotobiotic mice. I. Pathogenicity of Mycoplasma pneumoniae, Mycoplasma salivarium, and Mycoplasma pulmonis for the lungs of conventional and gnotobiotic mice. J Bacteriol. 1966 Oct;92(4):1154–1163. doi: 10.1128/jb.92.4.1154-1163.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. J Mol Biol. 1962 Jul;5:109–118. doi: 10.1016/s0022-2836(62)80066-7. [DOI] [PubMed] [Google Scholar]
- McGee Z. A., Rogul M., Falkow S., Wittler R. G. The relationship of Mycoplasma pneumoniae (Eaton agent) to Streptococcus MG: application of genetic tests to determine relatedness of L-forms and PPLO to bacteria. Proc Natl Acad Sci U S A. 1965 Aug;54(2):457–461. doi: 10.1073/pnas.54.2.457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NELSON J. B. Infection in laboratory animals with pleuropneumonia-like organisms. J Natl Cancer Inst. 1958 May;20(5):911–919. [PubMed] [Google Scholar]
- Organick A. B., Lutsky I. I. Pneumonia due to Mycoplasma in gnotobiotic mice. IV. Localization and identification of Mycoplasma pulmonis in the bronchi of infected gnotobiotic mice by immunofluorescence and by light microscopy. J Bacteriol. 1968 Jul;96(1):250–258. doi: 10.1128/jb.96.1.250-258.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Organick A. B., Siegesmund K. A., Lutsky I. I. Pneumonia due to mycoplasma in gnotobiotic mice. II. Localization of Mycoplasma pulmonis in the lungs of infected gnotobiotic mice by electron microscopy. J Bacteriol. 1966 Oct;92(4):1164–1176. doi: 10.1128/jb.92.4.1164-1176.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PEASE P. Bacterial origin of certain viruses: identity of the Eaton agent with Streptococcus MG. Nature. 1963 Mar 16;197:1132–1132. doi: 10.1038/1971132a0. [DOI] [PubMed] [Google Scholar]
- PEASE P. Evidence that Streptobacillus moniliformis is an intermediate stage between a corynebacterium and its L-form or derived PPLO. J Gen Microbiol. 1962 Sep;29:91–96. doi: 10.1099/00221287-29-1-91. [DOI] [PubMed] [Google Scholar]
- SMITH P. F., ROTHBLAT G. H. Relation of PPLO to bacteria. Ann N Y Acad Sci. 1960 Jan 15;79:461–464. doi: 10.1111/j.1749-6632.1960.tb42712.x. [DOI] [PubMed] [Google Scholar]
- Upton A. C., Jenkins V. K., Walburg H. E., Jr, Tyndall R. L., Conklin J. W., Wald N. Observations on viral, chemical, and radiation-induced myeloid and lymphoid leukemias in RF mice. Natl Cancer Inst Monogr. 1966 Sep;22:329–347. [PubMed] [Google Scholar]



