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  3. Polysaccharide capsule composition of pneumococcal serotype 19A subtypes: Unaltered among subtypes and independent of the nutritional environment
 

Polysaccharide capsule composition of pneumococcal serotype 19A subtypes: Unaltered among subtypes and independent of the nutritional environment

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BORIS DOI
10.7892/boris.87434
Publisher DOI
10.1128/IAI.00474-16
PubMed ID
27550933
Description
Serotype 19A strains have emerged as a cause of invasive pneumococcal disease after the introduction of the seven-valent pneumococcal conjugate vaccine (PCV7) and serotype 19A has now been included in the recent thirteen-valent vaccine (PCV13). Genetic analysis has revealed at least three different capsular serotype 19A subtypes and nutritional environment dependent variation of the 19A capsule structure has been reported. Pneumococcal vaccine effectiveness and serotyping accuracy might be impaired by structural differences in serotype 19A capsules. We therefore analyzed the distribution of 19A subtypes collected within a Swiss national surveillance program and determined capsule composition in different nutritional conditions with high-performance liquid chromatography (HPLC), gas chromatography – mass spectrometry (GC-MS) and nuclear magnetic resonance spectroscopy (NMR). After the introduction of PCV7 a significant relative increase of subtype 19A-II and decrease of 19A-I occurred. Chemical analyses showed no difference in the composition as well as the linkage of 19A subtype capsular saccharides grown in defined and undefined growth media being consistent with a trisaccharide repeat unit composed of rhamnose, N-acetyl-mannosamine and glucose. In summary, our study suggests that no structural variance dependent of the nutritional environment or the subtype exists. The serotype 19A subtype shift observed after the introduction of the PCV7 can therefore not be explained by selection of a capsule variant. However, capsule composition analysis of emerging 19A clones is recommended in cases where there is no other explanation for a selective advantage such as antibiotic resistance or loss or acquisition of other virulence factors
Date of Publication
2016-11
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)
Brugger, Silvioorcid-logo
Institut für Infektionskrankheiten
Troxler, Lukas
Institut für Infektionskrankheiten
Rüfenacht, Susanne
Institut für Infektionskrankheiten
Frey, Pascal Marcel
Universitätsklinik für Allgemeine Innere Medizin
Morand, Brigitte
Institut für Infektionskrankheiten, Forschung
Geyer, Rudolf
Mühlemann, Kathrin
Institut für Infektionskrankheiten
Höck, Stefan
Thormann, Wolfgang
Institut für Infektionskrankheiten, Labor für Klinische Pharmakologie
Furrer, Julienorcid-logo
Departement für Chemie und Biochemie (DCB)
Christen, Stephan
Lehrkörper, Medizinische Fakultät
Hilty, Markusorcid-logo
Institut für Infektionskrankheiten
Universitätsklinik für Infektiologie
Additional Credits
Institut für Infektionskrankheiten
Institut für Infektionskrankheiten, Labor für Klinische Pharmakologie
Departement für Chemie und Biochemie (DCB)
Lehrkörper, Medizinische Fakultät
Universitätsklinik für Allgemeine Innere Medizin
Institut für Infektionskrankheiten, Forschung
Series
Infection and immunity
Publisher
American Society for Microbiology
ISSN
0019-9567
Access(Rights)
open.access
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