Structural analysis of lipopolysaccharide produced by Heddleston serovars 10, 11, 12 and 15 and the identification of a new Pasteurella multocida lipopolysaccharide outer core biosynthesis locus, L6

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DOIResolve DOI: http://doi.org/10.1093/glycob/cwu030
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TypeArticle
Journal titleGlycobiology
ISSN1460-2423
Volume24
Issue7
Pages649659; # of pages: 11
Subjectbacterium lipopolysaccharide; glycosyltransferase; n acetylglucosamine; oligosaccharide; uridine diphosphate galactose; uridine diphosphate glucose; article; bacterial genetics; biosynthesis; capillary electrophoresis; carbohydrate analysis; electrospray mass spectrometry; gene duplication; gene mutation; genetic difference; genotype; heteronuclear single quantum coherence; methylation; nonhuman; nuclear Overhauser effect; Pasteurella multocida; priority journal; serotype; synteny
AbstractPasteurella multocida is a Gram-negative bacterial pathogen classified into 16 serovars based on lipopolysaccharide (LPS) antigens. Previously, we have characterized the LPS outer core biosynthesis loci L1, L2, L3, L5 and L7, and have elucidated the full range of LPS structures associated with each. In this study, we have determined the LPS structures produced by the type strains representing the serovars 10, 11, 12 and 15 and characterized a new LPS outer core biosynthesis locus, L6, common to all. The L6 outer core biosynthesis locus shares significant synteny with the L3 locus but due to nucleotide divergence, gene duplication and gene redundancy, the L6 and L3 LPS outer cores are structurally distinct. Using LPS structural and genetic differences identified in each L6 strain, we have predicted a role for most of the L6 glycosyltransferases in LPS assembly. Importantly, we have identified two glycosyltransferases, GctD and GatB, that differ by one amino acid, A162T, but use different donor sugars [uridine diphosphate (UDP)-Glc and UDP-Gal, respectively]. The longest outer core oligosaccharide, produced by the serovar 12 type strain, contained a terminal region consisting of β-Gal-(1,4)- β-GlcNAc-(1,3)-β-Gal-(1,4)-β-Glc that was identical in structure to the vertebrate glycosphingolipid, paragloboside. Mimicry of host glycosphingolipids has been observed previously in P. multocida strains belonging to L3 LPS genotype, which produce LPS similar in structure to the globo-series of glycosphingolipids. The expression of a paragloboside-like oligosaccharide on the LPS produced by the serovar 12 type strain indicates that strains belonging to the L6 LPS genotype may also engage in molecular mimicry. © The Author 2014.
Publication date
LanguageEnglish
AffiliationNational Research Council Canada (NRC-CNRC); Human Health Therapeutics (HHT-TSH)
Peer reviewedYes
NPARC number21272250
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Record identifier2b7ae920-d544-4978-9f1d-9f0a232cfa60
Record created2014-07-23
Record modified2016-05-09
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