Exopolysaccharides produced by clinical strains belonging to the Burkholderia cepacia complex

Abstract Background In the frame of a research line dedicated to better clarify the role of exopolysaccharides (EPS) in bacterial virulence, EPS produced by species of the Burkholderia cepacia complex (Bcc), namely Burkholderia multivorans , Burkholderia cenocepacia , and a Bcc member of undetermine...

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Veröffentlicht in:Journal of cystic fibrosis 2007-04, Vol.6 (2), p.145-152
Hauptverfasser: Herasimenka, Yury, Cescutti, Paola, Impallomeni, Giuseppe, Campana, Silvia, Taccetti, Giovanni, Ravenni, Novella, Zanetti, Flavio, Rizzo, Roberto
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Sprache:eng
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Zusammenfassung:Abstract Background In the frame of a research line dedicated to better clarify the role of exopolysaccharides (EPS) in bacterial virulence, EPS produced by species of the Burkholderia cepacia complex (Bcc), namely Burkholderia multivorans , Burkholderia cenocepacia , and a Bcc member of undetermined genomovar, all isolated at the Cystic Fibrosis Regional Centre of Florence (Italy), were investigated for they structural properties. Methods Three strains of B. multivorans , three of B. cenocepacia and one of a Bcc member of undetermined genomovar were isolated from CF patients. The reference strains C1576 and J2315, for genomovar II and III, respectively, were included in the study. The bacteria were grown on solid media, the exopolysaccharides produced were purified, and their structures were determined. In addition, sugar analysis of sputum samples was accomplished to search for EPS produced in vivo. Results Six strains out of seven produced the exopolysaccharide cepacian, while one strain of B. multivorans produced a completely different polymer, previously known in the literature as PS1. Two strains synthesised very small amounts of EPS. No definitive evidence for the presence of cepacian in sputum samples was found. Conclusions Most strains examined produced abundant amounts of polysaccharides. Cepacian was the most common EPS isolated and its production was not associated to a particular genomovar.
ISSN:1569-1993
1873-5010
DOI:10.1016/j.jcf.2006.06.004