Abstract
Sialylation of bacterial capsules has been proposed as an important virulence factor for several species of encapsulated pathogens, including group B Streptococcus. We have constructed a transposon mutant strain of type III group B Streptococcus that expresses a capsular polysaccharide differing from the wild type only in that the mutant strain's capsule lacks sialic acid. The mutant polysaccharide is antigenically identical to the capsular polysaccharide of type 14 Streptococcus pneumoniae, as predicted by the structures of the type III group B Streptococcus and S. pneumoniae polysaccharides. Loss of capsular sialic acid was associated with loss of virulence in the mutant strain in a neonatal rat model of lethal group B Streptococcus infection. These studies demonstrate directly that capsular sialic acid is a critical virulence determinant for type III group B Streptococcus and support the general hypothesis that surface sialylation aids pathogenic microorganisms in evading host defenses.
MeSH Terms
Bacterial Toxins/genetics
DNA Transposable Elements
Enzyme-Linked Immunosorbent Assay
Fluorescent Antibody Technique
Immunoblotting
Immunodiffusion
Microscopy, Electron
Mutation
Nucleic Acid Hybridization
Plasmids
Polysaccharides, Bacterial/genetics
Sialic Acids/analysis
Streptococcus agalactiae/genetics,pathogenicity,ultrastructure
Virulence
Chemicals
Bacterial Toxins
DNA Transposable Elements
Polysaccharides, Bacterial
Sialic Acids
streptococcal polysaccharide type III group B
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wessels M R
Channing Laboratory, Brigham and Women's Hospital, Boston, MA 02115.
Rubens C E
Benedí V J
Kasper D L
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