Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1987 Feb;55(2):314–319. doi: 10.1128/iai.55.2.314-319.1987

Effects of diet and genetics on Mycobacterium bovis BCG vaccine efficacy in inbred guinea pigs.

M K Cohen, R A Bartow, C L Mintzer, D N McMurray
PMCID: PMC260328  PMID: 3804439

Abstract

Strain 2 and strain 13 guinea pigs were vaccinated with Mycobacterium bovis BCG and placed on low-protein or protein-adequate diets. Five weeks later all animals were infected by the respiratory route with virulent Mycobacterium tuberculosis H37Rv organisms. Four weeks postchallenge, guinea pigs were skin tested with purified protein derivative and sacrificed. Protein deficiency resulted in significant reductions in body weight and thymus weight and in an impairment in the ability to control the M. bovis BCG vaccine organisms and to mount delayed hypersensitivity reactions. Protein deficiency also adversely affected the efficacy of the BCG vaccine as demonstrated by the numbers of virulent organisms recovered in spleens and lungs. Strain differences were observed in the number of leukocytes, thymus weight, and the responsiveness of blood lymphocytes to purified protein derivative stimulation. In general, strain 13 guinea pigs responded more dramatically to dietary insult than did their strain 2 counterparts. Protein deprivation completely abolished BCG vaccine protection in the lungs and spleens of strain 13 animals and significantly reduced the protection afforded to strain 2 animals. In both strains, the BCG vaccine protected normally nourished guinea pigs. There was no significant difference between strains with respect to susceptibility to pulmonary infection with virulent mycobacteria. Thus, diet and genetic pedigree each had a significant influence on BCG vaccine efficacy.

Full text

PDF
314

Selected References

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

  1. ALLISON M. J., ZAPPASODI P., LURIE M. B. Host-parasite relationships in natively resistant and susceptible rabbits on quantitative inhalation of tubercle bacilli. Their significance for the nature of genetic resistance. Am Rev Respir Dis. 1962 Apr;85:553–569. doi: 10.1164/arrd.1962.85.4.553. [DOI] [PubMed] [Google Scholar]
  2. Chaparas S. D. Immunity in tuberculosis. Bull World Health Organ. 1982;60(4):447–462. [PMC free article] [PubMed] [Google Scholar]
  3. Gros P., Skamene E., Forget A. Cellular mechanisms of genetically controlled host resistance to Mycobacterium bovis (BCG). J Immunol. 1983 Oct;131(4):1966–1972. [PubMed] [Google Scholar]
  4. Ho R. S., Fok J. S., Harding G. E., Smith D. W. Host-parasite relationships in experimental airborne tuberculosis. VII. Fate of Mycobacterium tuberculosis in primary lung lesions and in primary lesion-free lung tissue infected as a result of bacillemia. J Infect Dis. 1978 Aug;138(2):237–241. doi: 10.1093/infdis/138.2.237. [DOI] [PubMed] [Google Scholar]
  5. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  6. McMurray D. N., Carlomagno M. A., Cumberland P. A. Respiratory infection with attenuated Mycobacterium tuberculosis H37Ra in malnourished guinea pigs. Infect Immun. 1983 Feb;39(2):793–799. doi: 10.1128/iai.39.2.793-799.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. McMurray D. N., Carlomagno M. A., Mintzer C. L., Tetzlaff C. L. Mycobacterium bovis BCG vaccine fails to protect protein-deficient guinea pigs against respiratory challenge with virulent Mycobacterium tuberculosis. Infect Immun. 1985 Nov;50(2):555–559. doi: 10.1128/iai.50.2.555-559.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. McMurray D. N. Cell-mediated immunity in nutritional deficiency. Prog Food Nutr Sci. 1984;8(3-4):193–228. [PubMed] [Google Scholar]
  9. McMurray D. N., Loomis S. A., Casazza L. J., Rey H., Miranda R. Development of impaired cell-mediated immunity in mild and moderate malnutrition. Am J Clin Nutr. 1981 Jan;34(1):68–77. doi: 10.1093/ajcn/34.1.68. [DOI] [PubMed] [Google Scholar]
  10. McMurray D. N., Mintzer C. L., Tetzlaff C. L., Carlomagno M. A. The influence of dietary protein on the protective effect of BCG in guinea pigs. Tubercle. 1986 Mar;67(1):31–39. doi: 10.1016/0041-3879(86)90029-2. [DOI] [PubMed] [Google Scholar]
  11. McMurray D. N., Yetley E. A. Response to Mycobacterium bovis BCG vaccination in protein- and zinc-deficient guinea pigs. Infect Immun. 1983 Feb;39(2):755–761. doi: 10.1128/iai.39.2.755-761.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Orme I. M., Collins F. M. Demonstration of acquired resistance in Bcgr inbred mouse strains infected with a low dose of BCG montreal. Clin Exp Immunol. 1984 Apr;56(1):81–88. [PMC free article] [PubMed] [Google Scholar]
  13. Pavia C. S., Niederbuhl C. J. Adoptive transfer of anti-syphilis immunity with lymphocytes from Treponema pallidum-infected guinea pigs. J Immunol. 1985 Oct;135(4):2829–2834. [PubMed] [Google Scholar]
  14. Shevach E. M., Geczy A. F., deWeck A., Schwartz B. D. The guinea-pig I-region. III. Distribution of Ia antigens in inbred and partially inbred strains. J Immunogenet. 1980 Jun;7(3):229–242. doi: 10.1111/j.1744-313x.1980.tb00933.x. [DOI] [PubMed] [Google Scholar]
  15. Skamene E., Gros P., Forget A., Kongshavn P. A., St Charles C., Taylor B. A. Genetic regulation of resistance to intracellular pathogens. Nature. 1982 Jun 10;297(5866):506–509. doi: 10.1038/297506a0. [DOI] [PubMed] [Google Scholar]
  16. Smith D. W. Protective effect of BCG in experimental tuberculosis. Adv Tuberc Res. 1985;22:1–97. [PubMed] [Google Scholar]
  17. Stach J. L., Gros P., Forget A., Skamene E. Phenotypic expression of genetically-controlled natural resistance to Mycobacterium bovis (BCG). J Immunol. 1984 Feb;132(2):888–892. [PubMed] [Google Scholar]
  18. Wiegeshaus E. H., McMurray D. N., Grover A. A., Harding G. E., Smith D. W. Host-parasite relationships in experimental airborne tuberculosis. 3. Relevance of microbial enumeration to acquired resistance in guinea pigs. Am Rev Respir Dis. 1970 Sep;102(3):422–429. doi: 10.1164/arrd.1970.102.3.422. [DOI] [PubMed] [Google Scholar]
  19. Ziegler H. D., Ziegler P. B. Depression of tuberculin reaction in mild and moderate protein-calorie malnourished children following BCG vaccination. Johns Hopkins Med J. 1975 Aug;137(2):59–64. [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES