Immune response of BALB/c mice infected with two strains of Corynebacterium pseudotuberculosis

Igor Farias Tavares1, Maria da Conceição Aquino de Sá1, José Tadeu Raynal Rocha Filho1

  • 1Federal University of Bahia. Institute of Health Sciences, Salvador, Bahia, 40110-909, Brazil.

PubMed

Insights

This study compared immune responses in mice infected with two Corynebacterium pseudotuberculosis strains. The C57 strain caused greater changes and altered T cell and cytokine profiles compared to the T1 strain.

Area of Science:

  • Immunology
  • Microbiology
  • Veterinary Science

Background:

  • Corynebacterium pseudotuberculosis infections can cause significant disease in animals.
  • Understanding the differential immune responses to various strains is crucial for effective treatment and prevention.

Purpose of the Study:

  • To evaluate and compare the innate and adaptive immune responses in BALB/c mice infected with two distinct strains of Corynebacterium pseudotuberculosis (T1 and C57).
  • To identify specific immunological markers and morphological changes associated with each strain's infection.

Main Methods:

  • BALB/c mice were infected with C. pseudotuberculosis (T1 and C57 strains) for 70 days.
  • Morphological evaluation, and analysis of innate and adaptive immune responses including T cell populations (CD4+, CD8+) and cytokine profiles (IL-1α, IL-6, IL-13, IL-10, IL-2, IL-4, INF-γ, IL-22, IL-21, IL-27) were performed.

Main Results:

  • The C57 strain induced more severe morphological changes compared to the T1 strain.
  • Significant increases in CD4+ and CD8+ T cells were observed during C57 strain infection.
  • Distinct differences in inflammatory (IL-1α, IL-6) and regulatory (IL-13, IL-10) cytokine levels were noted between the groups.

Conclusions:

  • The study highlights differential immune responses elicited by C. pseudotuberculosis strains T1 and C57 in mice.
  • Findings contribute to understanding the immunological mechanisms underlying C. pseudotuberculosis infections, differentiating strain-specific effects.