Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1964 Aug 1;120(2):283–304. doi: 10.1084/jem.120.2.283

CORYNEBACTERIAL PSEUDOTUBERCULOSIS IN MICE

II. ACTIVATION OF NATURAL AND EXPERIMENTAL LATENT INFECTIONS

Robert M Fauve 1, Cynthia H Pierce-Chase 1, Rene Dubos 1
PMCID: PMC2137733  PMID: 14208250

Abstract

Latent corynebactenai infection occurs naturally in many strains of mice. It can be evoked into the active disease, pseudotuberculosis, by a single injection of 10 mg of cortisone. The cortisone effect was tested in 21 colonies, representing 11 genetically different strains of mice. Animals of the C57B1/6, DBA/2, and RIII strains were shown to be latently infected with Corynebacterium kutscheri by the fact that they developed fatal pseudotuberculosis following cortisone treatment. Virulent C. kutscheri could not be isolated from homogenates of organs obtained from latently infected animals before cortisone administration; however, these homogenates yielded small translucent colonies of avirulent organisms. Recovery of these atypical colonies was facilitated by preincubating the organ homogenates before plating. The organisms constituting such colonies differed morphologically and immunologically from C. kutscheri, but had similar biochemical properties with the exception that they lacked urease and catalase activity. Mice treated with cortisone yielded both the avirulent bacteria and virulent C. kutscheri. The latter was the predominant organism present in the organs at the height of infection. Injection of avirulent organisms into Swiss Lynch mice, which are normally free of latent corynebacteria, occasionally established a latent infection which could be converted into corynebacterial pseudotuberculosis by cortisone. Cultures of fully virulent C. kutscheri were then obtained from the lesions. Latency was produced experimentally with a streptomycin-resistant strain of virulent C. kutscheri (CKsr) derived from the stock culture. When sublethal doses of CKsr were injected into NCS mice (Institut Pasteur colony), they induced a latent infection characterized by the presence of avirulent organisms possessing the streptomycin resistance marker. These were isolated in the form of small translucent colonies from the livers of the infected animals. Administration of cortisone to these animals subsequently evoked active infection from which virulent CKsr could be obtained. Injection of the avirulent streptomycin-resistant organisms into normal NCS mice established a latent infection which could be uniformly converted into corynebacterial pseudotuberculosis by cortisone. The virulent C. kutscheri obtained from the lesions bore the genetic marker of streptomycin resistance, thus being identical with CKsr. Except for streptomycin resistance, the avirulent organisms isolated from the experimentally induced latent infections were identical with those found in the naturally occurring latent infections. These results suggest that C. kutscheri can persist in vitro in an avirulent form which is resistant to the defense mechanisms of the host, and can thus establish a latent infection. Treatment of the animal with cortisone results in the conversion of the avirulent form into virulent C. kutscheri, and of the latent infection into active corynebacterial pseudotuberculosis. The findings are discussed with regard to their relevance to infection immunity, and to the conversion of latent infection into overt disease.

Full Text

The Full Text of this article is available as a PDF (1.6 MB).

Selected References

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

  1. ANTOPOL W., GLAUBACH S., QUITTNER H. Experimental observations with massive doses of cortisone. Rheumatism. 1951 Jan;7(1):187–196. [PubMed] [Google Scholar]
  2. BATTISTO J. R., CHASE M. W. IMMUNOLOGICAL UNRESPONSIVENESS TO SENSITIZATION WITH SIMPLE CHEMICAL COMPOUNDS; A SEARCH FOR ANTIBODY-ABSORBING DEPOTS OF ALLERGEN. J Exp Med. 1963 Dec 1;118:1021–1035. doi: 10.1084/jem.118.6.1021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DIENES L., SHARP J. T. The role of high electrolyte concentration in the production and growth of L forms of bacteria. J Bacteriol. 1956 Feb;71(2):208–213. doi: 10.1128/jb.71.2.208-213.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DUBOS R., SCHAEDLER R. W. Some biological effects of the digestive flora. Am J Med Sci. 1962 Sep;244:265–271. doi: 10.1097/00000441-196209000-00001. [DOI] [PubMed] [Google Scholar]
  5. FAUVE R. M. R'ESISTANCE CELLULAIRE 'A L'INFECTION BACT'ERIENNE. I. R'ESISTANCE OPPOS'EE AU D'EVELOPPEMENT DE CORYNEBACTERIUM KUTSCHERI APR'ES SON INGESTION PAR DES MACROPHAGES DE SOURIS D'ORIGINES DIFF'ERENTES. Rev Fr Etud Clin Biol. 1964 Jan;9:100–105. [PubMed] [Google Scholar]
  6. FRIEDLANDER H., HABERMANN R. T., PARR L. W. Experimental arthritis in albino rats produced by a strain of Corynebacterium. J Infect Dis. 1951 May-Jun;88(3):290–297. doi: 10.1093/infdis/88.3.290. [DOI] [PubMed] [Google Scholar]
  7. Guze L. B., Kalmanson G. M. Persistence of Bacteria in "Protoplast" Form after Apparent Cure of Pyelonephritis in Rats. Science. 1964 Mar 20;143(3612):1340–1341. doi: 10.1126/science.143.3612.1340. [DOI] [PubMed] [Google Scholar]
  8. Lancefield R. C. THE ANTIGENIC COMPLEX OF STREPTOCOCCUS HAEMOLYTICUS : II. CHEMICAL AND IMMUNOLOGICAL PROPERTIES OF THE PROTEIN FRACTIONS. J Exp Med. 1928 Feb 29;47(3):469–480. doi: 10.1084/jem.47.3.469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LeMAISTRE C., TOMPSETT R. The emergence of pseudotuberculosis in rats given cortisone. J Exp Med. 1952 Apr;95(4):393–408. doi: 10.1084/jem.95.4.393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. MACPHERSON I. A., ALLNER K. L forms of bacteria as contaminants in tissue culture. Nature. 1960 Jun 18;186:992–992. doi: 10.1038/186992a0. [DOI] [PubMed] [Google Scholar]
  11. McDERMOTT W. Microbial persistence. Yale J Biol Med. 1958 Feb;30(4):257–291. [PMC free article] [PubMed] [Google Scholar]
  12. Meyer K. F. Latent Infections. J Bacteriol. 1936 Feb;31(2):109–135. doi: 10.1128/jb.31.2.109-135.1936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. PEASE P., LAUGHTON N. Observations on corynebacteria and related pleuropneumonia-like organisms (PPLO). J Gen Microbiol. 1962 Mar;27:383–389. doi: 10.1099/00221287-27-3-383. [DOI] [PubMed] [Google Scholar]
  14. PIERCE-CHASE C. H., FAUVE R. M., DUBOS R. CORYNEBACTERIAL PSEUDOTUBERCULOSIS IN MICE. I. COMPARATIVE SUSCEPTIBILITY OF MOUSE STRAINS TO EXPERIMENTAL INFECTION WITH CORYNEBACTERIUM KUTSCHERI. J Exp Med. 1964 Aug 1;120:267–281. doi: 10.1084/jem.120.2.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. PIERCE C. H., DUBOS R. J., SCHAEFER W. B. Multiplication and survival of tubercle bacilli in the organs of mice. J Exp Med. 1953 Feb 1;97(2):189–206. doi: 10.1084/jem.97.2.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. SERONDE J., Jr Resistance of rats to inoculation with Corynebacterium pathogenic in pantothenate deficiency. Proc Soc Exp Biol Med. 1954 Mar;85(3):521–524. doi: 10.3181/00379727-85-20938. [DOI] [PubMed] [Google Scholar]
  17. SERONDE J., Jr, ZUCKER L. M., ZUCKER T. F. The influence of duration of pantothenate deprivation upon natural resistance of rats to a Corynebacterium. J Infect Dis. 1955 Jul-Aug;97(1):35–38. doi: 10.1093/infdis/97.1.35. [DOI] [PubMed] [Google Scholar]
  18. SERONDE J., Jr, ZUCKER T. F., ZUCKER L. M. Thiamine, pyridoxine and pantothenic acid in the natural resistance of the rat to a Corynebacterium infection. J Nutr. 1956 Jun 10;59(2):287–298. doi: 10.1093/jn/59.2.287. [DOI] [PubMed] [Google Scholar]
  19. SHECHMEISTER I. L., ADLER F. L. Activation of pseudotuberculosis in mice exposed to sublethal total body radiation. J Infect Dis. 1953 May-Jun;92(3):228–239. doi: 10.1093/infdis/92.3.228. [DOI] [PubMed] [Google Scholar]
  20. SMITH P. F., PEOPLES D. M., MORTON H. E. Conversion of pleuropneumonialike organisms to bacteria. Proc Soc Exp Biol Med. 1957 Nov;96(2):550–553. doi: 10.3181/00379727-96-23536. [DOI] [PubMed] [Google Scholar]
  21. Swift H. F., Wilson A. T., Lancefield R. C. TYPING GROUP A HEMOLYTIC STREPTOCOCCI BY M PRECIPITIN REACTIONS IN CAPILLARY PIPETTES. J Exp Med. 1943 Aug 1;78(2):127–133. doi: 10.1084/jem.78.2.127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. TOBIN A. J., Jr, MORSE E. V. The pathogenicity of Corynebacterium pseudotuberculosis for laboratory white mice. Cornell Vet. 1957 Jul;47(3):413–418. [PubMed] [Google Scholar]
  23. VALLEE A., LEVADITI J. C. Abcès miliaires des reins observés chez le rat blanc et provoqués par un Corynebacterium aérobie voisin du type C. kutscheri. Ann Inst Pasteur (Paris) 1957 Oct;93(4):468–474. [PubMed] [Google Scholar]
  24. WITTLER R. G., CARY S. G., LINDBERG R. B. Reversion of a pleuropneumonia-like organism to a Corynebacterium during tissue culture passage. J Gen Microbiol. 1956 Jul;14(3):763–774. doi: 10.1099/00221287-14-3-763. [DOI] [PubMed] [Google Scholar]
  25. WITTLER R. G., MALIZIA W. F., KRAMER P. E., TUCKETT J. D., PRITCHARD H. N., BAKER H. J. Isolation of a Corynebacterium and its transitional forms from a case of subacute bacterial endocarditis treated with antibiotics. J Gen Microbiol. 1960 Oct;23:315–333. doi: 10.1099/00221287-23-2-315. [DOI] [PubMed] [Google Scholar]
  26. ZUCKER T. F., ZUCKER L. M. Pantothenic acid deficiency and loss of natural resistance to a bacterial infection in the rat. Proc Soc Exp Biol Med. 1954 Mar;85(3):517–521. [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES