Structural and Serological Characterization of Yet Another New O Antigen, O86, in Proteus mirabilis Clinical Strains

Int J Mol Sci. 2024 Dec 20;25(24):13642. doi: 10.3390/ijms252413642.

Abstract

Bacteria from the genus Proteus are facultative human pathogens, primarily attacking the urinary tract and wounds. A total of 85 O serogroups have been identified so far among these bacilli. P. mirabilis Bprz 86 was isolated from the fistula of a patient in Łódź, Poland. Enzyme-Linked Immunosorbent Assay (ELISA) and Western blotting studies involving the P. mirabilis Bprz 86 lipopolysaccharide (LPS) and the strain-specific rabbit antiserum indicated that the strain, which does not belong to any of the O1-O85 serogroups, shares a common epitope with Proteus O17 antigens and is identical to another clinical P. mirabilis strain, Sm 120, isolated from the urine of a patient in the area. The O-specific polysaccharide (O antigen) was obtained from P. mirabilis Bprz 86 LPS through mild acid degradation, and the six-constituent structure of its repeating unit was determined using chemical analyses and 1D and 2D 1H and 13C Nuclear Magnetic Resonance (NMR) spectroscopy. It includes (R)-3-hydroxybutanoyl, which, along with fucosamine and glucose residues, forms a fragment also present in the O17 antigens. Based on the obtained serological and chemical data, the two studied P. mirabilis isolates were proposed as candidates for a new successive O serogroup in the genus Proteus, O86.

Keywords: (R)-3-hydroxybutanoic acid; O-specific polysaccharide; chemical structure; epitope; lipopolysaccharide; serotyping.

MeSH terms

  • Animals
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Lipopolysaccharides / chemistry
  • Lipopolysaccharides / immunology
  • O Antigens* / chemistry
  • O Antigens* / immunology
  • Proteus Infections / diagnosis
  • Proteus Infections / immunology
  • Proteus Infections / microbiology
  • Proteus mirabilis* / immunology
  • Proteus mirabilis* / isolation & purification
  • Rabbits
  • Serogroup

Substances

  • O Antigens
  • Lipopolysaccharides

Grants and funding

This research received no external funding, the work was financially supported by the University of Lodz, Lodz, Poland.