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Type III group B streptococcal strain differences in susceptibility to opsonization with human serum
Pediatric Research
|December 1, 1981
Summary
Human serum antibodies to Group B Streptococcus (GBS) vary by strain. Immunization with a common antigen did not protect against all GBS strains, highlighting the need for functional antibody assays.
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Group B Streptococcus (GBS) is a significant pathogen.
- Human serum opsonins are crucial for combating GBS infections.
- Variability in GBS strain susceptibility to opsonization exists.
Purpose of the Study:
- To investigate human serum opsonin activity against type III GBS strains.
- To evaluate the efficacy of pneumococcal vaccine immunization in inducing opsonic antibodies to GBS.
- To identify bacterial factors contributing to GBS resistance to phagocytosis.
Main Methods:
- In vitro opsonophagocytic assay using human sera and type III GBS strains.
- Immunization of individuals with pneumococcal vaccine.
- Neuramindase treatment of GBS strains followed by fluorescent lectin-binding assay.
- Antibody absorption assays.
Main Results:
- Significant variability in serum opsonic titers against different type III GBS strains.
- Pneumococcal vaccine immunization primarily increased opsonic titers against susceptible GBS strains, not resistant ones.
- Neuramindase treatment rendered resistant GBS strains susceptible to neutrophil killing, suggesting sialic acid as an antiphagocytic factor.
- Both susceptible and resistant GBS strains absorbed opsonic antibodies, indicating antibody binding is not sufficient for phagocytosis.
Conclusions:
- Opsonic activity against one GBS strain does not predict activity against others.
- Core antigen immunization is insufficient to induce protective opsonic antibodies against all GBS strains.
- Functional antibody assays are essential, as antibody binding does not always correlate with bacterial killing.