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Published on: February 23, 2014
Group B streptococcal C protein-associated antigens: association with neonatal sepsis
Insights
The gamma antigen in group B streptococci (GBS) may be a virulence factor in early-onset sepsis. Most type III GBS strains express the c protein, but only the gamma antigen showed increased association with pathogenic strains.
Area of Science:
- Microbiology
- Immunology
- Neonatal infectious diseases
Background:
- Group B Streptococcus (GBS) is a leading cause of neonatal sepsis.
- The GBS c protein (Ibc) is linked to several antigens (alpha, beta, gamma, delta).
- The role of these antigens in GBS virulence is not fully understood.
Purpose of the Study:
- To evaluate the virulence potential of GBS c protein-associated antigens.
- To investigate the association of these antigens with GBS pathogenicity in neonates.
Main Methods:
- Serotyping of 255 GBS isolates from septic neonates, healthy neonates, and pregnant women.
- Radioimmunoassay using intact bacteria to detect GBS antigens.
- Survey for reactivity with sera to c protein and its associated antigens.
Main Results:
- Most (66%) type III GBS strains expressed the c protein, contrary to previous findings.
- The gamma antigen was significantly associated with early-onset GBS sepsis strains (P = .007).
- This association was independent of type-specific polysaccharide antigens.
Conclusions:
- The gamma antigen may serve as a potential virulence factor in GBS causing early-onset sepsis.
- Other c protein-associated antigens (alpha, beta, delta) did not show independent association with pathogenic strains.
Abstract:
The c protein (Ibc) of group B streptococci (GBS) is associated with at least four antigens (alpha, beta, gamma, delta). To assess the virulence potential of these antigens, 255 GBS isolates recovered from septic neonates, healthy neonates, and pregnant women were serotyped and surveyed for reactivity with sera to c protein and the four associated antigens. A radioimmunoassay using intact bacteria was used to detect the GBS antigens. In contrast to earlier reports, most (66%) of the type III strains expressed the c protein. Except for the gamma antigen, none of the other c protein-associated antigens showed an increased association with pathogenic strains independent of the polysaccharide antigens. The gamma antigen was expressed by 15 of 41 c protein-positive early-onset strains and by 4 of 38 c protein-positive late-onset strains (P = .007). This association was independent of the type-specific antigen, suggesting a potential role for the gamma antigen as a virulence factor in GBS strains causing early-onset sepsis.
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