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  3. Carbon source regulates polysaccharide capsule biosynthesis in Streptococcus pneumoniae
 

Carbon source regulates polysaccharide capsule biosynthesis in Streptococcus pneumoniae

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BORIS DOI
10.7892/boris.134050
Official URL
http://www.jbc.org/content/early/2019/10/08/jbc.RA119.010764.full.pdf
Publisher DOI
10.1074/jbc.RA119.010764
PubMed ID
31594867
Description
The exopolysaccharide capsule of Streptococcus pneumoniae is an important virulence factor, but the mechanisms that regulate capsule thickness are not fully understood. Here, we investigated the effects of various exogenously supplied carbohydrates on capsule production and gene expression in several pneumococcal serotypes. Microscopy analyses indicated a near absence of the capsular polysaccharide (CPS) when S. pneumoniae was grown in fructose. Moreover, serotype 7F pneumococci produced much less CPS than strains of other serotypes (6B, 6C, 9V, 15, and 23F) when grown on glucose or sucrose. RNA-Sequencing revealed carbon source–dependent regulation of distinct genes of wildtype strains and capsule-switch mutants of serotypes 6B and 7F, but could not explain the mechanism of capsule thickness regulation. In contrast, 31P NMR of whole-cell extract from capsule-knockout strains (Δcps) clearly revealed the accumulation or absence of capsule precursor metabolites when cells were grown on glucose or fructose, respectively. This finding suggests that fructose uptake mainly results in intracellular fructose-1-phosphate, which is not converted to CPS precursors. In addition, serotype 7F strains accumulated more precursors than did 6B strains, indicating less efficient conversion of precursor metabolites into the CPS in 7F, in line with its thinner capsule. Finally, isotopologue sucrose labeling and NMR analyses revealed that the uptake of the labeled fructose subunit into the capsule is < 10% that of glucose. Our findings on the effects of carbon sources on CPS production in different S. pneumoniae serotypes may contribute to a better understanding of pneumococcal diseases and could inform future therapeutic approaches
Date of Publication
2019-11-15
Publication Type
Article
Subject(s)
500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health
500 Science > 540 Chemistry
Language(s)
en
Contributor(s)
Troxler, Lukas
Institut für Infektionskrankheiten (IFIK)
Werren, Joel Pascal
Institut für Infektionskrankheiten, Forschung
Schaffner, Thierry O.
Mostacci, Nadezda
Institut für Infektionskrankheiten, Forschung
Vermathen, Peterorcid-logo
DIPR, Magnetresonanz-Spektroskopie und Methodologie (AMSM)
Department for BioMedical Research, Abt. Magnetresonanz-Spektroskopie und Methodologie, AMSM
Vermathen, Martina
Departement für Chemie und Biochemie (DCB)
Wüthrich, Daniel
Simillion, Cedric
Brugger, Silvio D.
Bruggmann, Rémy
Bioinformatik und computerbasierte Biologie
Hathaway, Lucy Janeorcid-logo
Institut für Infektionskrankheiten, Forschung
Furrer, Julienorcid-logo
Departement für Chemie und Biochemie (DCB)
Hilty, Markusorcid-logo
Institut für Infektionskrankheiten (IFIK)
Additional Credits
Bioinformatik und computerbasierte Biologie
Institut für Infektionskrankheiten, Forschung
Departement für Chemie und Biochemie (DCB)
Institut für Infektionskrankheiten (IFIK)
DIPR, Magnetresonanz-Spektroskopie und Methodologie (AMSM)
Series
Journal of biological chemistry
Publisher
American Society for Biochemistry and Molecular Biology
ISSN
0021-9258
Access(Rights)
open.access
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