Structure and genetic basis of Yersinia similis serotype O:9 O-specific polysaccharide

Author:

Beczała Agnieszka12,Ovchinnikova Olga G3,Datta Neeta4,Mattinen Laura4,Knapska Katarzyna4,Radziejewska-Lebrecht Joanna2,Holst Otto1,Skurnik Mikael45

Affiliation:

1. Division of Structural Biochemistry, Research Center Borstel, Leibniz-Center for Medicine and Biosciences, Airway Research Center North (ARCN), Borstel, Germany

2. Department of Microbiology, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland

3. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia

4. Department of Bacteriology and Immunology, Haartman Institute, and Research Programs Unit, Immunobiology, University of Helsinki, Helsinki, Finland

5. Helsinki University Central Hospital Laboratory Diagnostics, Helsinki, Finland

Abstract

The O-polysaccharide (OPS, O-Ag) cap of LPS is a major virulence factor of Yersinia species and also serves as a receptor for the binding of lytic bacteriophage φR1-37. Currently, the OPS-based serotyping scheme for the Yersinia pseudotuberculosis complex includes 21 known O-serotypes that follow three distinct lineages: Y. pseudotuberculosis sensu stricto, Y. similis and the Korean group of strains. Elucidation of the Y. pseudotuberculosis complex OPS structures and characterization of the OPS genetics (altogether 18 O-serotypes studied thus far) allows a better understanding of the relationships among the various O serotypes and will facilitate the analysis of the evolutionary processes giving rise to new serotypes. Here we present the characterization of the OPS structure and gene cluster of Y. similis O:9. Bacteriophage φR1-37, which uses the Y. similis O:9 OPS as a receptor, also infects a number of Y. enterocolitica serotypes, including O:3, O:5,27, O:9 and O:50. The Y. similis O:9 OPS structure resembled none of the receptor structures of the Y. enterocolitica strains, suggesting that φR1-37 can recognize several surface receptors, thus promoting broad host specificity.

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

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