Proteomic analysis of Proteus mirabilis outer membrane proteins reveals differential expression in vivo vs. in vitro

Bruno D'Alessandro1, Leticia M S Lery, Wanda M A von Krüger

  • 1Departamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Montevideo, Uruguay.

Insights

Proteus mirabilis outer membrane proteins (OMPs) were analyzed in vivo versus in vitro. Iron-regulated OMPs are expressed and immunogenic during infection, suggesting roles in virulence.

Area of Science:

  • Microbiology
  • Proteomics
  • Pathogenesis

Background:

  • Proteus mirabilis is an opportunistic pathogen causing urinary tract infections.
  • Outer membrane proteins (OMPs) are crucial for bacterial survival and interaction.
  • Understanding OMPs in vivo is key to deciphering virulence factors.

Purpose of the Study:

  • To compare in vivo and in vitro outer membrane protein expression of Proteus mirabilis.
  • To identify iron-regulated outer membrane proteins and their expression patterns.
  • To investigate the role of specific proteins and host interactions in P. mirabilis pathogenesis.

Main Methods:

  • Proteomic analysis of P. mirabilis grown in vivo and in vitro under varying iron conditions.
  • Identification of differentially expressed outer membrane proteins.
  • Western blot analysis using sera from infected mice to assess immunogenicity.

Main Results:

  • Three iron receptors (IreA, PMI0842, PMI2596) were identified in vivo and in vitro under iron restriction.
  • A prophage gene product (PMI1721) was exclusively detected in vivo.
  • Host plasminogen co-purified with in vivo OMPs, indicating potential virulence association.
  • Iron-regulated proteins were found to be immunogenic during infection.

Conclusions:

  • Proteomic analysis reveals distinct OMP profiles in vivo versus in vitro.
  • Iron-regulated outer membrane proteins are immunogenic and likely contribute to P. mirabilis virulence.
  • Further research into PMI1721 and plasminogen interaction may uncover novel virulence mechanisms.