Systemic immunization with rPotD reduces Streptococcus pneumoniae nasopharyngeal colonization in mice

T R Converso1, C Goulart2, D Rodriguez2

  • 1Centro de Biotecnologia, Instituto Butantan, São Paulo, Brazil; Programa de Pós Graduação Interunidades em Biotecnologia USP-IPT-IB, São Paulo, Brazil.

Vaccine
|November 26, 2016
PubMed

Insights

Subcutaneous immunization with the pneumococcal protein PotD reduced bacterial load in mice. This protection was linked to antibody-induced phagocytosis and cellular immune responses, suggesting PotD as a vaccine candidate.

Area of Science:

  • Immunology
  • Microbiology
  • Vaccinology

Background:

  • Streptococcus pneumoniae (pneumococcus) causes severe infections like meningitis and pneumonia.
  • The pneumococcal protein PotD is part of the PotABCD polyamine transporter complex and is crucial for virulence.
  • Developing new protein-based vaccines against pneumococcal colonization is a public health priority.

Purpose of the Study:

  • To evaluate the efficacy of subcutaneous immunization with recombinant PotD (rPotD) in a mouse model of pneumococcal colonization.
  • To investigate the antibody and cellular immune responses induced by rPotD immunization.
  • To assess the potential of PotD as a component of a novel pneumococcal vaccine.

Main Methods:

  • Mice were subcutaneously immunized with rPotD.
  • Immunized mice were intranasally challenged with type 6B pneumococcus.
  • Bacterial load in nasal tissue was quantified.
  • Antibody levels, bacterial phagocytosis by peritoneal cells, and cellular immune responses (gamma-interferon, IL-2, IL-17, nitric oxide) were measured.

Main Results:

  • Subcutaneous immunization with rPotD significantly reduced pneumococcal bacterial load in mouse nasal tissue.
  • rPotD immunization induced high levels of antibodies that enhanced bacterial phagocytosis by peritoneal cells.
  • Cellular immune responses included gamma-interferon, IL-2, and IL-17 production by splenocytes and nitric oxide production by peritoneal cells.

Conclusions:

  • PotD is a promising candidate for a protein-based pneumococcal vaccine.
  • rPotD vaccination induces protective immunity characterized by phagocytic antibodies and a Th1/IL-17 cellular response.
  • PotD-based vaccination may reduce nasopharyngeal colonization, a key event in pneumococcal transmission.

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