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Updated: Oct 19, 2025

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Group B streptococcal infections in infants in Iceland: clinical and microbiological factors
Birta Baeringsdottir1, Helga Erlendsdottir1,2, Erla Soffia Bjornsdottir2
1Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Insights
Group B Streptococcus (GBS) clonal complex 17 (CC17) is a significant cause of late-onset GBS infections in Icelandic infants. This CC is linked to increasing LOD cases, highlighting the need for a GBS vaccine.
Area of Science:
- Neonatal infectious diseases
- Microbiology and immunology
- Epidemiology
Background:
- Group B Streptococcus (GBS) is a primary cause of invasive neonatal infections, categorized as early-onset disease (EOD) and late-onset disease (LOD).
- Different GBS clonal complexes (CCs) are associated with distinct disease presentations and timings.
- Understanding GBS CCs' roles is crucial for developing targeted prevention strategies.
Purpose of the Study:
- To investigate infant GBS infections in Iceland between 1975 and 2019.
- To determine if specific GBS CCs correlate with disease presentation (sepsis, meningitis, pneumonia) and timing (EOD vs. LOD).
- To assess the prevalence of GBS CC17 in infant GBS infections in Iceland.
Main Methods:
- Retrospective analysis of all culture-confirmed invasive GBS infections in infants (<90 days) in Iceland (1975-2019).
- Collection of clinical data from medical records.
- Identification and analysis of GBS clonal complexes.
Main Results:
- A total of 105 infants were included, with 56 EOD cases and 49 LOD cases.
- GBS infections declined from 2000 but increased late in the study period; LOD incidence significantly increased over time (P=0.0001).
- GBS CC17 (serotype III) accounted for approximately one-third of cases and was significantly associated with LOD (P<0.001).
Conclusions:
- GBS CC17 is a predominant cause of infant GBS infections in Iceland, specifically linked to LOD.
- The rising incidence of LOD, particularly CC17-associated cases, is a concern.
- A GBS vaccine is essential for preventing LOD, as current intrapartum antibiotic prophylaxis primarily targets EOD.
Abstract:
Introduction. Group B streptococcus (GBS) is a leading cause of invasive neonatal infections. These have been divided into early-onset disease (EOD; <7 days) and late-onset disease (LOD; 7-89 days), with different GBS clonal complexes (CCs) associated with different disease presentations.Hypothesis. Different GBS CCs are associated with timing of infection (EOD or LOD) and clinical presentation (sepsis, meningitis or pneumonia).Aim. To study infant GBS infections in Iceland from 1975 to 2019. Are specific GBS CCs related to disease presentation? Is CC17 overrepresented in infant GBS infections in Iceland?Methodology. All culture-confirmed invasive GBS infections in infants (<90 days) in Iceland from 1975 to 2019 were included. Clinical information was gathered from medical records.Results. A total of 127 invasive GBS infections in infants were diagnosed, but 105 infants were included in the study. Of these, 56 had EOD and 49 had LOD. The incidence of GBS infections declined from 2000 onwards but increased again at the end of the study period. Furthermore, there was a significant increase in LOD over the study period (P=0.0001). The most common presenting symptoms were respiratory difficulties and fever and the most common presentation was sepsis alone. Approximately one-third of the cases were caused by GBS CC17 of serotype III with surface protein RIB and pili PI-1+PI-2b or PI-2b. CC17 was significantly associated with LOD (P<0.001).Conclusion. CC17 is a major cause of GBS infection in infants in Iceland. This clone is associated with LOD, which has been increasing in incidence. Because intrapartum antibiotic prophylaxis only prevents EOD, it is important to continue the development of a GBS vaccine in order to prevent LOD infections.
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