The Complex World of Polysaccharides 2012
DOI: 10.5772/50116
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Capsular Polysaccharides Produced by the Bacterial Pathogen Burkholderia pseudomallei

Abstract: The Complex World of Polysaccharides 132 the weakly virulent B. thailandensis (6.8 x 10 5 CFU) [42]. This demonstrated that SR1015 is severely attenuated for virulence in this animal model of melioidosis and that type I O-PS is a major virulence determinant of B. pseudomallei. We later determined that the type I O-PS was a capsular polysaccharide (CPS I), not an O-PS moiety, which will be discussed below.

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Cited by 8 publications
(4 citation statements)
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“…B. pseudomallei encodes a highly immunogenic capsular polysaccharide (CPS-I), and a type II O-antigenic polysaccharide (O-PS) moiety of lipopolysaccharide (LPS), both of which are required for serum resistance and virulence (61, 62). We have previously documented a 1-bp loss-of-function indel within the CPS-I gene, wcbR , which occurred prior to retrieval of the first isolate and which persisted throughout the duration of the chronic-carriage infection (14).…”
Section: Resultsmentioning
confidence: 99%
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“…B. pseudomallei encodes a highly immunogenic capsular polysaccharide (CPS-I), and a type II O-antigenic polysaccharide (O-PS) moiety of lipopolysaccharide (LPS), both of which are required for serum resistance and virulence (61, 62). We have previously documented a 1-bp loss-of-function indel within the CPS-I gene, wcbR , which occurred prior to retrieval of the first isolate and which persisted throughout the duration of the chronic-carriage infection (14).…”
Section: Resultsmentioning
confidence: 99%
“…Only CF11 exhibited a mutation in CPS-I, with the latter isolate encoding a 1-bp deletion in wcbA ( BPSL2809 ). WcbA, a capsular export protein, is critical for B. pseudomallei virulence (62). This mutation causes a frameshift at residue A434 that truncates this protein by 70 amino acids and likely abrogates CPS-I production in this strain.…”
Section: Resultsmentioning
confidence: 99%
“…In sea ice, bacteria may acquire similar protection by producing capsular polysaccharides, as genes involved in transporting and exporting capsular polysaccharide components were more abundant there (Supplementary Table 4). These EPS remain intimately associated with the cell surface, where they can act as an antibiotic (and possible viral) shield, while also aiding in surface attachment and biofilm formation (Reckseidler-Zenteno, 2012) or cryoprotection (Carillo et al, 2015).…”
Section: Elaborate Competitive Strategies At High Cell Densities In Subzero Brinesmentioning
confidence: 99%
“…[1] Thecapsular polysaccharides protect the microorganism from adverse environmental conditions,prevent the activation of the host immune system and improve adhesion to invade the host. [2][3][4] Capsular polysaccharides of pathogens have been used to produce vaccines that are effective in adults, [5,6] but result ineffective in children below 2years of age: [7][8][9] being T-cell-independent antigens,t hey do not induce B-cell memory and do not stimulate the production of immunoglobulin G( IgG). However,aT-cell-dependent response (thus inducing B-cell memory) can be obtained by chemical coupling of polysaccharides to immunogenic proteins.P olysaccharide-protein conjugates are commonly obtained by covalent linkage of reactive precursors to the e-amino groups of surface-exposed lysine residues or other reactive amino acids.…”
mentioning
confidence: 99%