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Heat-killed Streptococcus suis capsular type 2 strains stimulate tumor necrosis factor alpha and interleukin-6

M Segura1, J Stankova, M Gottschalk

  • 1Groupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP), Faculté de Médecine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec, Canada.

Infection and Immunity
|August 24, 1999
PubMed

Insights

Streptococcus suis type 2 triggers macrophages to release inflammatory cytokines tumor necrosis factor alpha (TNF-alpha) and interleukin-6 (IL-6). This response is crucial for initiating swine meningitis and has implications for zoonotic disease.

Area of Science:

  • Immunology
  • Microbiology
  • Pathogenesis

Background:

  • * Streptococcus suis capsular type 2 is a significant cause of swine meningitis and a zoonotic pathogen.
  • * Mononuclear phagocytes are implicated in meningitis pathogenesis.
  • * Understanding S. suis interactions with immune cells is vital for disease control.

Purpose of the Study:

  • * To investigate the capacity of killed S. suis type 2 to induce proinflammatory cytokine release (TNF-alpha and IL-6) from murine macrophages.
  • * To determine the role of phagocytosis and bacterial components in this cytokine induction.
  • * To explore the differential induction of TNF-alpha and IL-6.

Main Methods:

  • * Murine macrophages were stimulated with whole killed S. suis type 2, its components, or controls (LPS).
  • * Cytokine production (TNF-alpha, IL-6) was measured with and without phorbol 12-myristate 13-acetate (PMA) costimulation.
  • * Experiments utilized cytochalasin-treated macrophages and an unencapsulated mutant to assess phagocytosis dependence.
  • * Purified capsular polysaccharide and cell wall components were tested for cytokine-inducing activity.

Main Results:

  • * S. suis type 2 induced concentration- and time-dependent release of TNF-alpha and IL-6.
  • * Cytokine production was enhanced by PMA costimulation and was phagocytosis-independent.
  • * The S. suis cell wall, but not the capsular polysaccharide, induced both TNF-alpha and IL-6.
  • * An unencapsulated mutant induced TNF-alpha but not IL-6, suggesting distinct stimuli for each cytokine.

Conclusions:

  • * S. suis type 2 effectively stimulates macrophages to produce key proinflammatory cytokines.
  • * The bacterial cell wall is a significant driver of this immune response.
  • * Phagocytosis is not required for S. suis-induced cytokine production.
  • * This macrophage activation likely contributes to the initiation and progression of S. suis meningitis.

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