Intravenous administration of Streptococcus mutans induces IgA nephropathy-like lesions

Clin Exp Nephrol. 2020 Dec;24(12):1122-1131. doi: 10.1007/s10157-020-01961-1. Epub 2020 Sep 9.

Abstract

Background: IgA nephropathy (IgAN) is one of the most frequently occurring types of chronic glomerulonephritis. Previous analyses have revealed that a major pathogen of dental caries, Streptococcus mutans [which expresses collagen-binding protein (Cnm) on its surface], is involved in the pathogenesis of IgAN.

Methods: Cnm-positive S. mutans isolated from a patient with IgAN was intravenously administered to specific pathogen-free Sprague-Dawley rats to evaluate their kidney conditions.

Results: The urinary protein level of the S. mutans group reached a plateau at 30 days, with increased numbers of mesangial cells and an increased mesangial matrix. The numbers of rats with IgA-positive and/or C3-positive glomeruli were significantly greater in the S. mutans group than in the control group at 45 days (P < 0.05). Electron microscopy analyses revealed electron-dense depositions in the mesangial area among rats in the S. mutans group. There were significantly more CD68-positive cells (macrophages) in the glomeruli of the S. mutans group than in the glomeruli of the control group during the late phase (P < 0.05), similar to the findings in patients with IgAN.

Conclusion: Our results suggested that intravenous administration of Cnm-positive S. mutans caused transient induction of IgAN-like lesions in rats.

Keywords: Dental caries; Glomerulonephritis; IgA nephropathy; Intravenous administration; Rats; Streptococcus mutans.

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Complement C3 / metabolism
  • Disease Models, Animal
  • Glomerulonephritis, IGA / immunology
  • Glomerulonephritis, IGA / microbiology*
  • Glomerulonephritis, IGA / pathology
  • Humans
  • Immunoglobulin A / metabolism
  • Kidney / immunology
  • Kidney / microbiology*
  • Kidney / ultrastructure
  • Macrophages / immunology
  • Macrophages / microbiology
  • Male
  • Rats, Sprague-Dawley
  • Streptococcal Infections / complications
  • Streptococcal Infections / microbiology*
  • Streptococcus mutans / isolation & purification
  • Streptococcus mutans / pathogenicity*
  • Time Factors

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 protein, rat
  • Complement C3
  • Immunoglobulin A