Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1983 Feb;39(2):865–872. doi: 10.1128/iai.39.2.865-872.1983

Mycobacterium leprae infection in nude mice: bacteriological and histological responses to primary infection and large inocula.

R D Lancaster, G R Hilson, A C McDougall, M J Colston
PMCID: PMC348028  PMID: 6339392

Abstract

Previous studies have demonstrated that congenitally athymic, nude mice are highly susceptible to infection with Mycobacterium leprae. In this study, we showed that footpad inoculation of nude mice with different inoculum sizes of M. leprae resulted in exponential growth of bacilli until bacillary numbers reached approximately 10(10) bacilli per footpad. There was dissemination of the infection from approximately 10 months after inoculation. When nude mice were compared with thymectomized and irradiated mice and normal intact mice for the ability to detect growth from large inocula of low viability, nude mice were the most sensitive, permitting the detection of 10(2) viable M. leprae among 10(7) irradiation-killed organisms. There was widespread dissemination of the infection throughout the reticuloendothelial system and the tissues of the cooler body sites from approximately 10 months after inoculation. Histologically, the lesions resembled those seen in lepromatous leprosy, although the bacillary load appeared larger and was similar to that seen in heavily infected tissues of the nine-banded armadillo. An unusual feature was the presence of numerous foci of neutrophil polymorphs in the footpads and liver of infected nude mice.

Full text

PDF
865

Images in this article

Selected References

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

  1. Cheers C., Waller R. Activated macrophages in congenitally athymic "nude mice" and in lethally irradiate mice. J Immunol. 1975 Sep;115(3):844–847. [PubMed] [Google Scholar]
  2. Colston M. J., Hilson G. R. Growth of Mycobacterium leprae and M. marinum in congenitally athymic (nude) mice. Nature. 1976 Jul 29;262(5567):399–401. doi: 10.1038/262399a0. [DOI] [PubMed] [Google Scholar]
  3. Cutler J. E. Acute systemic candidiasis in normal and congenitally thymic-deficient (nude) mice. J Reticuloendothel Soc. 1976 Feb;19(2):121–124. [PubMed] [Google Scholar]
  4. Dawson P. J., Ringus J. C., Fieldsteel A. H. Neonatally thymectomized Lewis rats infected with Mycobacterium leprae. 2. Histopathologic and electron microscopic observations. Int J Lepr Other Mycobact Dis. 1979 Dec;47(4):561–569. [PubMed] [Google Scholar]
  5. Emmerling P., Finger H., Bockemühl J. Listeria monocytogenes infection in nude mice. Infect Immun. 1975 Aug;12(2):437–439. doi: 10.1128/iai.12.2.437-439.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fieldsteel A. H., Levy L. Dapsone chemotherapy of Mycobacterium leprae infection of the neonatally thymectomized Lewis rat. Am J Trop Med Hyg. 1976 Nov;25(6):854–859. doi: 10.4269/ajtmh.1976.25.854. [DOI] [PubMed] [Google Scholar]
  7. Holmes I. B., Hilson G. R. The effect of rifampicin and dapsone on experimental Mycobacterium leprae infections: minimum inhibitory concentrations and bactericidal action. J Med Microbiol. 1972 May;5(2):251–261. doi: 10.1099/00222615-5-2-251. [DOI] [PubMed] [Google Scholar]
  8. Job C. K., Kirchheimer W. F., Sanchez R. M. Liver lesions in experimental lepromatoid leprosy of the armadillo. A histopathologic study. Int J Lepr Other Mycobact Dis. 1978 Jan-Mar;46(1):1–8. [PubMed] [Google Scholar]
  9. Kirchheimer W. F., Storrs E. E., Binford C. H. Attempts to establish the Armadillo (Dasypus novemcinctus linn.) as a model for the study of leprosy. II. Histopathologic and bacteriologic post-mortem findings in lepromatoid leprosy in the Armadillo. Int J Lepr Other Mycobact Dis. 1972 Jul-Sep;40(3):229–242. [PubMed] [Google Scholar]
  10. Kohsaka K., Mori T., Ito T. Lepromatoid lesion developed in nude mouse inoculated with Mycobacterium leprae--animal transmission of leprosy. Repura. 1976 Jul-Sep;45(3):177–187. doi: 10.5025/hansen1930.45.3_177. [DOI] [PubMed] [Google Scholar]
  11. Rees R. J. Enhanced susceptibility of thymectomized and irradiated mice to infection with Mycobacterium leprae. Nature. 1966 Aug 6;211(5049):657–658. doi: 10.1038/211657a0. [DOI] [PubMed] [Google Scholar]
  12. Rees R. J., Waters M. F., Pearson J. M., Helmy H. S., Laing A. B. Long-term treatment of dapsone-resistant leprosy with rifampicin: clinical and bacteriological studies. Int J Lepr Other Mycobact Dis. 1976 Jan-Jun;44(1-2):159–169. [PubMed] [Google Scholar]
  13. Rees R. J., Weddell A. G. Biology of the mycobacterioses. Experimental models for studying leprosy. Ann N Y Acad Sci. 1968 Sep 5;154(1):214–236. doi: 10.1111/j.1749-6632.1968.tb16711.x. [DOI] [PubMed] [Google Scholar]
  14. Shepard C. C., McRae D. H. A method for counting acid-fast bacteria. Int J Lepr Other Mycobact Dis. 1968 Jan-Mar;36(1):78–82. [PubMed] [Google Scholar]
  15. Weddell A. G., Palmer E., Rees R. J. The fate of Mycobacterium leprae in CBA mice. J Pathol. 1971 Jun;104(2):77–92. doi: 10.1002/path.1711040202. [DOI] [PubMed] [Google Scholar]

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

RESOURCES