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Published on: February 23, 2014
Group B streptococcal infection: a review and update
Insights
Group B Streptococcus (GBS) causes serious infant infections. Preventive measures like immunisation or antibiotics during labour can protect newborns from GBS disease.
Area of Science:
- Neonatal infectious diseases
- Bacterial pathogenesis
- Public health microbiology
Background:
- Group B Streptococcus (GBS) infections in infants have increased significantly since the 1970s.
- Neonatal GBS disease presents as early-onset or late-onset infections.
- Approximately 1% of infants born to colonized mothers develop GBS infection, with high mortality rates.
Purpose of the Study:
- To describe and discuss the challenges posed by the rising incidence of severe group B streptococcal disease in infants.
- To review the epidemiology, clinical presentation, and mortality associated with neonatal GBS infections.
- To evaluate potential preventive strategies for GBS disease in newborns.
Main Methods:
- Literature review and synthesis of existing data on GBS infections in infants.
- Analysis of disease incidence, transmission dynamics from mother to infant, and treatment outcomes.
- Examination of experimental evidence for preventive interventions.
Main Results:
- Infants born to GBS-colonized mothers have a high risk of acquiring the organism.
- Early-onset GBS disease has a 30% mortality rate even with prompt antibiotic treatment.
- Late-onset GBS disease, while less fatal, can occur up to two months after birth.
Conclusions:
- Effective preventive strategies are crucial to combat the rising threat of neonatal GBS disease.
- Active or passive immunization and intrapartum intravenous ampicillin are demonstrated protective measures.
- Prompt medical intervention is vital, but preventative approaches offer the best outcomes for infants at risk.
Abstract:
The problems posed by the sudden increase in serious group B streptococcal disease among infants since the early 1970s are described and discussed. Virtually all offspring of colonised mothers harbour the organism and infection develops in about 1% of these infants. The mortality rate, even with immediate antibiotic treatment of early onset disease, is 30%; delay in treatment leads to much higher mortality. Late onset disease starting around the seventh to ninth day of life, but sometimes as late as the second month, is less frequently fatal. Preventive measures include active and passive immunisation or intravenous ampicillin during labour. Experimental evidence indicates that each of these methods gives protection.
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