Outer membrane antigens of the uropathogen Proteus mirabilis recognized by the humoral response during experimental

Greta R Nielubowicz1, Sara N Smith, Harry L T Mobley

  • 1Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109-0620, USA.

Insights

Proteus mirabilis causes urinary tract infections. Researchers identified 37 potential vaccine targets, including iron acquisition proteins PMI0842 and PMI2596, which are crucial for bacterial fitness during infection.

Area of Science:

  • Microbiology
  • Immunology
  • Vaccine Development

Background:

  • Proteus mirabilis is a significant cause of complicated urinary tract infections (cUTIs).
  • Identifying surface-exposed antigens is crucial for developing effective vaccines against P. mirabilis.

Purpose of the Study:

  • To systematically identify surface-exposed antigens of Proteus mirabilis as potential vaccine candidates.
  • To evaluate the role of identified antigens in bacterial virulence during urinary tract infections.

Main Methods:

  • Proteins from the outer membrane of P. mirabilis were separated using two-dimensional gel electrophoresis.
  • Western blotting with infected mouse sera and mass spectrometry were employed for antigen identification.
  • Genome sequencing and comparative analysis aided in pinpointing surface-exposed antigens.
  • Virulence studies were conducted using gene-mutated P. mirabilis strains in a murine UTI model.

Main Results:

  • Thirty-seven antigens, including 23 outer membrane proteins, were identified, indicating a humoral immune response.
  • Mutations in genes PMI0047, rafY, and fadL did not attenuate P. mirabilis in the murine UTI model.
  • Putative iron acquisition proteins, PMI0842 and PMI2596, were found to contribute significantly to bacterial fitness in the urinary tract.

Conclusions:

  • PMI0842 and PMI2596 are promising vaccine candidates due to their role in P. mirabilis fitness and potential antigenicity.
  • Further research is warranted to explore the protective efficacy of these identified antigens.

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