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Journal of Bacteriology, November 1999, p. 6937-6947, Vol. 181, No. 22
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Immunochemical Characterization and Taxonomic Evaluation of the O Polysaccharides of the Lipopolysaccharides of Pseudomonas syringae Serogroup O1 Strains

Vladimir V. Ovod,1,* Yuriy A. Knirel,2 Regine Samson,3 and Kai J. Krohn1

Institute of Medical Technology, University of Tampere, Tampere, Finland1; N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia2; and Pathologie Vegetale, Institut National de la Recherche Agronomique, Beaucouze Cedex, France3

Received 7 May 1999/Accepted 30 August 1999

The O polysaccharide (OPS) of the lipopolysaccharide (LPS) of Pseudomonas syringae pv. atrofaciens IMV 7836 and some other strains that are classified in serogroup O1 was shown to be a novel linear alpha -D-rhamnan with the tetrasaccharide O repeat right-arrow3)-alpha -D-Rhap-(1right-arrow3)-alpha -D-Rhap-(1right-arrow2)-alpha -D-Rhap-(1right-arrow2)-alpha -D-Rhap-(1right-arrow (chemotype 1A). The same alpha -D-rhamnan serves as the backbone in branched OPSs with lateral (alpha 1right-arrow3)-linked D-Rhap, (beta 1right-arrow4)-linked D-GlcpNAc, and (alpha 1right-arrow4)-linked D-Fucf residues (chemotypes 1B, 1C, and 1D, respectively). Strains of chemotype 1C demonstrated variations resulting in a decrease of the degree of substitution of the backbone 1A with the lateral D-GlcNAc residue (chemotype 1C-1A), which may be described as branched regular left-right-arrow  branched irregular right-arrow linear OPS structure alterations (1Cleft-right-arrow 1C-1A right-arrow 1A). Based on serological data, chemotype 1D was suggested to undergo a 1D left-right-arrow  1D-1A alteration, whereas chemotype 1B showed no alteration. A number of OPS backbone-specific monoclonal antibodies (MAbs), Ps(1-2)a, Ps(1-2)a1, Ps1a, Ps1a1, and Ps1a2, as well as MAbs Ps1b, Ps1c, Ps1c1, Ps1d, Ps(1-2)d, and Ps(1-2)d1 specific to epitopes related to the lateral sugar substituents of the OPSs, were produced against P. syringae serogroup O1 strains. By using MAbs, some specific epitopes were inferred, serogroup O1 strains were serotyped in more detail, and thus, the serological classification scheme of P. syringae was improved. Screening with MAbs of about 800 strains representing all 56 known P. syringae pathovars showed that the strains classified in serogroup O1 were found among 15 pathovars and the strains with the linear OPSs of chemotype 1A were found among 9 of the 15 pathovars. A possible role for the LPS of P. syringae and related pseudomonads as a phylogenetic marker is discussed.


* Corresponding author. Mailing address: Institute of Medical Technology, University of Tampere, P.O. Box 607, Tampere FIN-33101, Finland. Phone: (358-3) 215-7757. Fax: (358-3) 215-7332. E-mail: Ltvlov{at}uta.fi.


Journal of Bacteriology, November 1999, p. 6937-6947, Vol. 181, No. 22
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



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