PRESENCE OF 1-7 GALACTURONIC TRANSFERASES IN LABORATORY AND CLINICAL PROTEUS MIRABILIS STRAINS

Wieslaw Kaca Lukasz Lechowicz Paulina Zarnowiec Marek Kwinkowski
Department of Microbiology, Jan Kochanowski University, Kielce

Proteus mirabilis stains are  opportunistic pathogens of humans causing numerous infections. In our bioinformatics reseach we have shown that the gene PMI2517 present in the genome of P. mirabilis is a homologous to the gene wabO from Klebsiella paeumoniae. In structural studies of P. mirabilis lipopolysaccharides (LPSs) indicate that galaktouronic acids (GalA) are component of the O-specific polysaccharide parts as well as in core region of LPSs [1]. Aim of this study was to identify 1→7 galaktouronic acid transferases of LPSs core oligosaccharide 45 laboratory and clinical P. mirabilis strains.

In all tested DNA samples isolated from tested P. mirabilis strains  PCR  products with a length 540 bp were identified. Restriction analysis of PCR products was carried out with endonuclease Sau3AI. Based on the bioinformatics analysis 1→7 galaktouronic acid transferase genes sequences  expected two electrophoretic bands (corresponding to DNA fragments with a length 407 and 134 bp) were detected. The presence of the 1→7 galaktouronic acid transferase genes in all 45 tested Proteus mirabilis strains was shown. It is worth to stressing that the 1→7 galaktouronic acid transferase gene was identify in DNA from Re type of deep rough mutant - P. mirabilis R45 strain. LPS P. mirabilis R45 do not contain GalA residues. In conclusion - we demonstrated the possibility of using unique 1→7 galaktouronic acid transferase gene amplification techniques for Proteus species specific identification.

1- Knirel YA et al. W. Structure and serology of O-antigens as the basis for classification of Proteus strains. Innate Immun 17, 2011, 70-96.

Acknowledgements: This work was supported by grant N N304 275540 from CSC Poland and POIG 2.2. Poland







 




Powered by Eventact EMS