Humoral and cellular immune responses in mice against secreted and somatic antigens from a Corynebacterium pseudotuberculosis attenuated strain: Immune response against a C. pseudotuberculosis strain

BMC Vet Res. 2016 Sep 8;12(1):195. doi: 10.1186/s12917-016-0811-8.

Abstract

Background: Corynebacterium pseudotuberculosis is the etiologic agent of caseous lymphadenitis (CL), a chronic disease that affects goats and sheep. CL is characterized by the formation of granulomas in lymph nodes and other organs, such as the lungs and liver. Current knowledge of CL pathogenesis indicates that the induction of humoral and cellular immune responses are fundamental to disease control. The aim of this study was to evaluate the humoral and cellular immune responses in BALB/c mice inoculated with a C. pseudotuberculosis strain isolated in the state of Bahia, Brazil.

Results: The lymphocyte proliferation and in vitro production of IFN-γ, IL-4, IL-10, IL-12 and nitric oxide by spleen cells stimulated with secreted and somatic antigens from the studied strain were evaluated. IgG subclasses were also analyzed. Results showed a significant increase of Th1-profile cytokines after 60 days post-inoculation, as well as an important humoral response, represented by high levels of IgG2a and IgG1 against C. pseudotuberculosis.

Conclusion: The T1 strain of C. pseudotuberculosis was shown to induce humoral and cellular immune responses in BALB/c mice, but, even at a dosage of 1x10(7) CFU, no signs of the disease were observed.

Keywords: BALB/c; Corynebacterium pseudotuberculosis; Cytokines; IgG isotypes.

MeSH terms

  • Animals
  • Antigens, Bacterial / immunology*
  • Bacterial Vaccines / immunology*
  • Cells, Cultured
  • Corynebacterium Infections / microbiology
  • Corynebacterium Infections / prevention & control*
  • Corynebacterium pseudotuberculosis / metabolism*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Immunity, Cellular
  • Immunity, Humoral
  • Mice
  • Mice, Inbred BALB C
  • Spleen / cytology
  • Spleen / metabolism

Substances

  • Antigens, Bacterial
  • Bacterial Vaccines
  • Cytokines