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Comparative analysis of clinics, pathologies and immune responses in BALB/c and C57BL/6 mice infected with

Juliane Fornefett1, Jaqueline Krause2, Kristin Klose3

  • 1Institute for Bacteriology and Mycology, Faculty of Veterinary Medicine, University Leipzig, Leipzig, Germany.

Microbes and Infection
|October 13, 2017
PubMed

Insights

Streptobacillus moniliformis intranasal infection causes high mortality and severe pathology in C57BL/6 mice, inducing a Th1 immune response. BALB/c mice showed resistance and a Th2 response, indicating strain-specific susceptibility and immune reactions.

Area of Science:

  • Immunology
  • Microbiology
  • Pathology

Background:

  • Streptobacillus moniliformis is a zoonotic pathogen associated with rats.
  • Intranasal infection models are crucial for studying respiratory pathogens.
  • Mouse strains exhibit differential susceptibility to infections.

Purpose of the Study:

  • To investigate the immune response and pathology following intranasal Streptobacillus moniliformis infection in C57BL/6 and BALB/c mice.
  • To compare the susceptibility and distinct pathologies induced by S. moniliformis in different mouse strains.
  • To characterize the immune response, specifically Th1 vs. Th2, in susceptible and resistant mouse models.

Main Methods:

  • Intranasal inoculation of Streptobacillus moniliformis in C57BL/6 and BALB/c mice.
  • Assessment of mortality rates and clinical signs.
  • Histopathological examination of affected tissues (lymph nodes, lungs).
  • Serological analysis including IgG subclass differentiation (IgG2b/IgG1 ratio).

Main Results:

  • C57BL/6 mice exhibited high susceptibility (75% mortality) with severe purulent lymphadenitis and pneumonia.
  • BALB/c mice showed resistance, with no signs of disease.
  • Significant seroconversion occurred in surviving mice of both strains.
  • C57BL/6 mice displayed a Th1 immune response (IgG2b/IgG1 ratio of 2.5), while BALB/c mice showed a Th2 response (ratio < 0.5).
  • Standard sentinel systems may be insufficient for infection detection.

Conclusions:

  • Intranasal S. moniliformis infection elicits strain-dependent pathologies and immune responses in mice.
  • C57BL/6 mice serve as a valuable model for studying S. moniliformis-induced Th1-mediated pathology.
  • BALB/c mice are resistant, exhibiting a Th2-biased response.
  • Diagnostic limitations highlight the need for comprehensive monitoring strategies.

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