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. 1984 Apr;51(4):711–717.

Listeriosis in beige mice and their heterozygous littermates.

C Cheers, P Wood
PMCID: PMC1454538  PMID: 6706378

Abstract

The ability to resist the facultative intracellular bacterium Listeria monocytogenes was not impaired in the beige mutants of C57BL/6J mice which are known to be deficient in a number of immune functions. The intravenous LD50 of Listeria in beige (bg/bg) mice and their normal heterozygous (bg +) littermates was approximately 5 X 10(5). Growth of Listeria in the spleen and liver during primary and secondary infections was similar in the two groups of mice, and each was able to act efficiently in adoptive transfer of immunity. Histological examination showed a normal accumulation of polymorphonuclear and mononuclear cells at foci of infection in the liver, while in the spleen the previously described depletion of T cells 2-4 days after infection was observed in both groups. In-vitro 18-hr cytotoxicity of peritoneal cells for P815 targets, a function usually attributed to macrophages, was increased 2 days after infection in both bg/bg and bg/+ mice. In contrast, 4 hr cytotoxicity of spleen cells for YAC-1 targets, considered typical of natural killer (NK) cells, was depressed in uninfected bg/bg mice and only slightly raised during infection. This compared with a normal NK activity in uninfected bg/+ mice which was markedly increased during infection.

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Selected References

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

  1. Bancroft G. J., Shellam G. R., Chalmer J. E. Genetic influences on the augmentation of natural killer (NK) cells during murine cytomegalovirus infection: correlation with patterns of resistance. J Immunol. 1981 Mar;126(3):988–994. [PubMed] [Google Scholar]
  2. Boyle W. An extension of the 51Cr-release assay for the estimation of mouse cytotoxins. Transplantation. 1968 Sep;6(6):761–764. doi: 10.1097/00007890-196809000-00002. [DOI] [PubMed] [Google Scholar]
  3. Chan Y. Y., Cheers C. Mechanism of depletion of T lymphocytes from the spleen of mice infected with Listeria monocytogenes. Infect Immun. 1982 Nov;38(2):686–693. doi: 10.1128/iai.38.2.686-693.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chan Y. Y., Cheers C. Recovery from T cell depletion during murine listeriosis and effect on a T-dependent antibody response. Infect Immun. 1982 Nov;38(2):694–698. doi: 10.1128/iai.38.2.694-698.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cheers C., McKenzie I. F., Pavlov H., Waid C., York J. Resistance and susceptibility of mice to bacterial infection: course of listeriosis in resistant or susceptible mice. Infect Immun. 1978 Mar;19(3):763–770. doi: 10.1128/iai.19.3.763-770.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cheers C., McKenzie I. F. Resistance and susceptibility of mice to bacterial infection: genetics of listeriosis. Infect Immun. 1978 Mar;19(3):755–762. doi: 10.1128/iai.19.3.755-762.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Elin R. J., Edelin J. B., Wolff S. M. Infection and immunoglobulin concentrations in Chediak-Higashi mice. Infect Immun. 1974 Jul;10(1):88–91. doi: 10.1128/iai.10.1.88-91.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hansson M., Kärre K., Kiessling R., Roder J., Andersson B., Häyry P. Natural NK-cell targets in the mouse thymus: characteristics of the sensitive cell population. J Immunol. 1979 Aug;123(2):765–771. [PubMed] [Google Scholar]
  9. Hirsch R. L. Natural killer cells appear to play no role in the recovery of mice from Sindbis virus infection. Immunology. 1981 May;43(1):81–89. [PMC free article] [PubMed] [Google Scholar]
  10. Holmberg L. A., Springer T. A., Ault K. A. Natural killer activity in the peritoneal exudates of mice infected with Listeria monocytogenes: characterization of the natural killer cells by using a monoclonal rat anti-murine macrophage antibody (M1/70). J Immunol. 1981 Nov;127(5):1792–1799. [PubMed] [Google Scholar]
  11. Johnson K. J., Varani J., Oliver J., Ward P. A. Immunologic vasculitis in beige mice with deficiency of leukocytic neutral protease. J Immunol. 1979 May;122(5):1807–1811. [PubMed] [Google Scholar]
  12. Keller R. Macrophage-mediated natrual cytotoxicity against various target cells in vitro. I. Macrophages from diverse anatomical sites and different strains of rats and mice. Br J Cancer. 1978 May;37(5):732–741. doi: 10.1038/bjc.1978.111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kiessling R. W., Welsh R. M., Jr Killing of normal cells by activated mouse natural killer cells: evidence for two patterns of genetic regulation of lysis. Int J Cancer. 1980 May 15;25(5):611–615. doi: 10.1002/ijc.2910250510. [DOI] [PubMed] [Google Scholar]
  14. Lawrence D. A., Schell R. F. Susceptibility of C5-deficient mice to listeriosis: modulation by Concanavalin A. Cell Immunol. 1978 Sep;39(2):336–344. doi: 10.1016/0008-8749(78)90109-0. [DOI] [PubMed] [Google Scholar]
  15. Mahoney K. H., Morse S. S., Morahan P. S. Macrophage functions in beige (Chédiak-Higashi syndrome) mice. Cancer Res. 1980 Nov;40(11):3934–3939. [PubMed] [Google Scholar]
  16. Mandel T. E., Cheers C. Resistance and susceptibility of mice to bacterial infection: histopathology of listeriosis in resistant and susceptible strains. Infect Immun. 1980 Dec;30(3):851–861. doi: 10.1128/iai.30.3.851-861.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Murphy J. W., McDaniel D. O. In vitro reactivity of natural killer (NK) cells against Cryptococcus neoformans. J Immunol. 1982 Apr;128(4):1577–1583. [PubMed] [Google Scholar]
  18. Nunn M. E., Herberman R. B., Holden H. T. Natural cell-mediated cytotoxicity in mice against non-lymphoid tumor cells and some normal cells. Int J Cancer. 1977 Sep 15;20(3):381–387. doi: 10.1002/ijc.2910200309. [DOI] [PubMed] [Google Scholar]
  19. Oliver C., Essner E. Formation of anomalous lysosomes in monocytes, neutrophils, and eosinophils from bone marrow of mice with Chédiak-Higashi syndrome. Lab Invest. 1975 Jan;32(1):17–27. [PubMed] [Google Scholar]
  20. Piccini A. E., Jahreis G. P., Novak E. K., Swank R. T. Intracellular distribution of lysosomal enzymes in the mouse pigment mutants pale ear and pallid. Mol Cell Biochem. 1980 Jun 18;31(2):89–95. doi: 10.1007/BF00240814. [DOI] [PubMed] [Google Scholar]
  21. Roder J. C., Lohmann-Matthes M. L., Domzig W., Kiessling R., Haller O. A functional comparison of tumor cell killing by activated macrophages and natural killer cells. Eur J Immunol. 1979 Apr;9(4):283–288. doi: 10.1002/eji.1830090407. [DOI] [PubMed] [Google Scholar]
  22. Roder J., Duwe A. The beige mutation in the mouse selectively impairs natural killer cell function. Nature. 1979 Mar 29;278(5703):451–453. doi: 10.1038/278451a0. [DOI] [PubMed] [Google Scholar]
  23. Root R. K., Rosenthal A. S., Balestra D. J. Abnormal bactericidal, metabolic, and lysosomal functions of Chediak-Higashi Syndrome leukocytes. J Clin Invest. 1972 Mar;51(3):649–665. doi: 10.1172/JCI106854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Stevenson M. M., Kongshavn P. A., Skamene E. Genetic linkage of resistance to Listeria monocytogenes with macrophage inflammatory responses. J Immunol. 1981 Aug;127(2):402–407. [PubMed] [Google Scholar]
  25. Tagliabue A., Mantovani A., Kilgallen M., Herberman R. B., McCoy J. L. Natural cytotoxicity of mouse monocytes and macrophages. J Immunol. 1979 Jun;122(6):2363–2370. [PubMed] [Google Scholar]
  26. Vassalli J. D., Granelli-Piperno A., Griscelli C., Reich E. Specific protease deficiency in polymorphonuclear leukocytes of Chédiak-Higashi syndrome and beige mice. J Exp Med. 1978 Apr 1;147(4):1285–1290. doi: 10.1084/jem.147.4.1285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Welsh R. M., Jr, Kiessling R. W. Natural killer cell response to lymphocytic choriomeningitis virus in beige mice. Scand J Immunol. 1980;11(4):363–367. doi: 10.1111/j.1365-3083.1980.tb00001.x. [DOI] [PubMed] [Google Scholar]
  28. Windhorst D. B., Padgett G. The Chediak-Higashi syndrome and the homologous trait in animals. J Invest Dermatol. 1973 Jun;60(6):529–537. doi: 10.1111/1523-1747.ep12703609. [DOI] [PubMed] [Google Scholar]

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