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. 1962 Nov 30;116(6):847–857. doi: 10.1084/jem.116.6.847

MEASUREMENT OF RESISTANCE TO EXPERIMENTAL TUBERCULOSIS IN MICE

THE HYPERACUTE PHASE

Richard Costello 1, Rene Dubos 1, Russell W Schaedler 1
PMCID: PMC2137587  PMID: 14023313

Abstract

NCS mice were found to be susceptible to a hyperacute form of disease induced by injection of relatively large doses of Mycobacterium tuberculosis. Susceptibility to this type of disease was conditioned by the sex, age, and dietary history of the animals. Unlike the more usual response of mice to mycobacterial disease, these conditions affected primarily the relative occurrence of early-acute deaths rather than average survival time. Resistance to this form of disease was increased by previous exposure of the animals to Gram-negative bacteria, to their endotoxin, or to various preparations of killed mycobacterial cells.

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Selected References

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

  1. DUBOS R. J., SCHAEDLER R. W. The effect of bacterial endotoxins on the water intake and body weight of mice. J Exp Med. 1961 May 1;113:921–934. doi: 10.1084/jem.113.5.921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. DUBOS R. J., SCHAEDLER R. W. The effect of diet on the fecal bacterial flora of mice and on their resistance to infection. J Exp Med. 1962 Jun 1;115:1161–1172. doi: 10.1084/jem.115.6.1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DUBOS R. J., SCHAEDLER R. W. The effect of the intestinal flora on the growth rate of mice, and on their susceptibility to experimental infections. J Exp Med. 1960 Mar 1;111:407–417. doi: 10.1084/jem.111.3.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. HEDGECOCK L. W. Antagonism of the inhibitory action of aminosalicylic acid on Mycobacterium tuberculosis by methionine, biotin and certain fatty acids, amino acids, and purines. J Bacteriol. 1956 Dec;72(6):839–846. doi: 10.1128/jb.72.6.839-846.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. SCHAEDLER R. W., DUBOS R. J. The fecal flora of various strains of mice. Its bearing on their susceptibility to endotoxin. J Exp Med. 1962 Jun 1;115:1149–1160. doi: 10.1084/jem.115.6.1149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. SCHAEDLER R. W., DUBOS R. J. The susceptibility of mice to bacterial endotoxins. J Exp Med. 1961 Mar 1;113:559–570. doi: 10.1084/jem.113.3.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. WILLIAMS C. A., Jr Studies on fractions of methanol extracts of tubercle bacilli. II. Toxic and allergenic properties of fractions employed as antituberculous vaccine. J Exp Med. 1960 Mar 1;111:369–386. doi: 10.1084/jem.111.3.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. YOUMANS G. P., YOUMANS A. S. The measurement of the response of immunized mice to infection with Mycobacterium tuberculosis va. hominis. J Immunol. 1957 May;78(5):318–329. [PubMed] [Google Scholar]

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