Chemokine production induced by Corynebacterium pseudotuberculosis in a murine model

Braz J Microbiol. 2022 Jun;53(2):1019-1027. doi: 10.1007/s42770-022-00694-5. Epub 2022 Feb 9.

Abstract

Corynebacterium pseudotuberculosis is the etiological agent of caseous lymphadenitis. The main clinical sign of this disease is the development of granulomas, especially in small ruminants; however, the pathways that are involved in the formation and maintenance of these granulomas are unknown. Cytokines and chemokines are responsible for the migration of immune cells to specific sites and tissues; therefore, it is possible that chemokines participate in abscess formation. This study aimed to evaluate the induction of chemokine production by two C. pseudotuberculosis strains in a murine model. A highly pathogenic (VD57) and an attenuated (T1) strain of C. pseudotuberculosis, as well as somatic and secreted antigens derived from these strains, was used to stimulate murine splenocytes. Then, the concentrations of the chemokines CCL-2, CCL-3, CCL-4, and CCL-5 and the cytokines IL-1 and TNF were measured in the culture supernatants. The VD57 strain had a higher ability to stimulate the production of chemokines when compared to T1 strain, especially in the early stages of stimulation, which can have an impact on granuloma formation. The T1 lysate antigen was able to stimulate most of the chemokines studied herein when compared to the other antigenic fractions of both strains. These results indicate that C. pseudotuberculosis is a chemokine production inducer, and the bacterial strains differ in their induction pattern, a situation that can be related to the specific behavior of each strain.

Keywords: Caseous lymphadenitis; Chemotaxis; Corynebacteriaceae; Granuloma.

MeSH terms

  • Animals
  • Corynebacterium Infections* / microbiology
  • Corynebacterium Infections* / veterinary
  • Corynebacterium pseudotuberculosis*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Lymphadenitis* / microbiology
  • Mice

Substances

  • Cytokines