Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1956 Oct 31;104(5):737–762. doi: 10.1084/jem.104.5.737

FATE OF MYCOBACTERIUM TUBERCULOSIS IN MOUSE TISSUES AS DETERMINED BY THE MICROBIAL ENUMERATION TECHNIQUE

I. THE PERSISTENCE OF DRUG-SUSCEPTIBLE TUBERCLE BACILLI IN THE TISSUES DESPITE PROLONGED ANTIMICROBIAL THERAPY

Robert M McCune Jr 1, Ralph Tompsett 1
PMCID: PMC2136613  PMID: 13367341

Abstract

Observations are presented on the behavior of populations of tubercle bacilli in the tissues of mice during the administration of antimicrobial drugs. The behavior of the populations during therapy with any particular drug was different depending upon whether the tubercle bacilli were subsisting in the lung or in the spleen. Moreover, the pattern of microbial behavior was distinctive and predictable for each drug studied. Changes in the size of the populations of tubercle bacilli in the tissues appeared to be a more sensitive reflection of drug influence than microscopic study of the number and character of the tuberculous lesions. Nevertheless, in untreated animals, pulmonary lesions evolved and progressed steadily to a fatal outcome despite the fact that the populations of tubercle bacilli had stabilized at a relatively high census early in the course of therapy. The uniform persistence of tubercle bacilli in the spleen throughout prolonged drug administration was demonstrated with every drug or multiple drug regimens except for pyrazinamide when accompanied by isoniazid. Cultures of the bacilli which survived in the tissues despite antimicrobial therapy were highly susceptible to the drugs employed when tested in vitro. Thus the survival of the tubercle bacilli in the tissues represented microbial persistence rather than drug resistance. When pyrazinamide and isoniazid were administered together, it was not possible to detect the microorganisms in the spleen or lungs of treated animals. A detailed investigation of this apparent abolition of microbial persistence forms the subject of an accompanying report.

Full Text

The Full Text of this article is available as a PDF (2.1 MB).

Selected References

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

  1. MCCUNE R. M., Jr, MCDERMOTT W., TOMPSETT R. The fate of Mycobacterium tuberculosis in mouse tissues as determined by the microbial enumeration technique. II. The conversion of tuberculous infection to the latent state by the administration of pyrazinamide and a companion drug. J Exp Med. 1956 Nov 1;104(5):763–802. doi: 10.1084/jem.104.5.763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. McDERMOTT W., ORMOND L., MUSCHENHEIM C., DEUSCHLE K., McCUNE R. M., Jr, TOMPSETT R. Pyrazinamide-isoniazid in tuberculosis. Am Rev Tuberc. 1954 Mar;69(3):319–333. doi: 10.1164/art.1954.69.3.319. [DOI] [PubMed] [Google Scholar]
  3. TOMPSETT R., McCUNE R. M., Jr, ORMOND L., DEUSCHLE K., MUSCHENHEIM C., McDERMOTT W. The influence of pyrazinamide-isoniazid on M. tuberculosis in animals and man. Trans Assoc Am Physicians. 1954;67:224–231. [PubMed] [Google Scholar]
  4. WEDUM A. G. Nonautomatic pipetting devices for the microbiologic laboratory. J Lab Clin Med. 1950 Apr;35(4):648–651. [PubMed] [Google Scholar]
  5. YEAGER R. L., MUNROE W. G. C., DESSAU F. I. Pyrazinamide (aldinamide) in the treatment of pulmonary tuberculosis. Am Rev Tuberc. 1952 May;65(5):523–546. [PubMed] [Google Scholar]

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

RESOURCES