Publication:
Pneumococcal serotype determines growth and capsule size in human cerebrospinal fluid

cris.virtual.author-orcid0000-0002-5361-5397
cris.virtualsource.author-orcideebc9c2e-1eaa-46fc-b92b-c2ab55bfe1af
cris.virtualsource.author-orcid1a98c672-42f1-4388-8fc7-f85f67de333d
cris.virtualsource.author-orcidfe74547e-3739-4ea8-ac81-baad9000ff19
cris.virtualsource.author-orcid8d01fcca-a0eb-4a30-9de2-264db009608e
datacite.rightsopen.access
dc.contributor.authorMüller, Annelies Kathrin
dc.contributor.authorSalmen, Anke
dc.contributor.authorAebi, Susanne
dc.contributor.authorde Gouveia, Linda
dc.contributor.authorvon Gottberg, Anne
dc.contributor.authorHathaway, Lucy Jane
dc.date.accessioned2024-10-28T18:26:39Z
dc.date.available2024-10-28T18:26:39Z
dc.date.issued2020-01-20
dc.description.abstractBackground: The polysaccharide capsule is a major virulence factor of S. pneumoniae in diseases such as meningitis. While some capsular serotypes are more often found in invasive disease, high case fatality rates are associated with those serotypes more commonly found in asymptomatic colonization. We tested whether growth patterns and capsule size in human cerebrospinal fluid depends on serotype using a clinical isolate of S. pneumoniae and its capsule switch mutants. Results: We found that the growth pattern differed markedly from that in culture medium by lacking the exponential and lysis phases. Growth in human cerebrospinal fluid was reduced when strains lost their capsules. When a capsule was present, growth was serotype-specific: high carriage serotypes (6B, 9V, 19F and 23F) grew better than low carriage serotypes (7F, 14, 15B/C and 18C). Growth correlated with the case-fatality rates of serotypes reported in the literature. Capsule size in human cerebrospinal fluid also depended on serotype. Conclusions: We propose that serotype-specific differences in disease severity observed in meningitis patients may, at least in part, be explained by differences in growth and capsule size in human cerebrospinal fluid. This information could be useful to guide future vaccine design.
dc.description.numberOfPages9
dc.description.sponsorshipInstitut für Infektionskrankheiten, Forschung
dc.description.sponsorshipUniversitätsklinik für Neurologie
dc.identifier.doi10.7892/boris.139460
dc.identifier.pmid31959125
dc.identifier.publisherDOI10.1186/s12866-020-1700-7
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/186441
dc.language.isoen
dc.publisherBioMed Central
dc.relation.ispartofBMC microbiology
dc.relation.issn1471-2180
dc.relation.organizationDCD5A442BA19E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BAE0E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BD12E17DE0405C82790C4DE2
dc.relation.schoolDCD5A442C27BE17DE0405C82790C4DE2
dc.subjectStreptococcus pneumoniae
dc.subjecthuman cerebrospinal fluid
dc.subjectserotype
dc.subjectcapsule
dc.subjectgrowth
dc.subjectcase fatality rate
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.titlePneumococcal serotype determines growth and capsule size in human cerebrospinal fluid
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPage16
oaire.citation.volume20
oairecerif.author.affiliationInstitut für Infektionskrankheiten, Forschung
oairecerif.author.affiliationUniversitätsklinik für Neurologie
oairecerif.author.affiliationInstitut für Infektionskrankheiten, Forschung
oairecerif.author.affiliationInstitut für Infektionskrankheiten, Forschung
unibe.contributor.rolecreator
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unibe.date.licenseChanged2020-02-05 10:31:08
unibe.description.ispublishedpub
unibe.eprints.legacyId139460
unibe.journal.abbrevTitleBMC MICROBIOL
unibe.refereedtrue
unibe.subtype.articlejournal

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