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A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Invasive Group B Streptococcus Disease With Recurrence and in Multiples: Towards a Better Understanding of GBS
Mirjam Freudenhammer1,2,3, Konstantinos Karampatsas4, Kirsty Le Doare4
1Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Group B Streptococcus (GBS) can cause late-onset invasive disease (iGBS) in infants. Recurrent or multiple births increase iGBS risk, suggesting microbiome disturbances and host immunity factors play a role.
Area of Science:
- Neonatal Medicine
- Infectious Diseases
- Microbiology
Background:
- Group B Streptococcus (GBS) commonly colonizes the gut in newborns.
- While often asymptomatic, GBS can lead to late-onset invasive GBS disease (iGBS), including sepsis or meningitis, in a small percentage of infants.
- The transmission routes and specific risk factors for iGBS, particularly in recurrent cases and multiple births, remain incompletely understood.
Purpose of the Study:
- To investigate shared and fixed risk factors for invasive Group B Streptococcus disease (iGBS).
- To analyze cases of recurrent iGBS and iGBS occurring in twins/triplets to understand disease dynamics and contributing factors.
Main Methods:
- Analysis of iGBS cases with recurrence (n=25) and in twins/triplets (n=32).
- Data sourced from a UK/Ireland national surveillance study (2014/15) and a retrospective case collection from Germany and Switzerland.
- Statistical analysis to identify risk factors and disease onset intervals.
Main Results:
- Infants from multiple births faced a high risk (17%) of iGBS if a sibling was already affected.
- The onset interval for iGBS between siblings was 4.5 days, and for recurrent cases, it was 12.5 days.
- Increased risk of recurrence was associated with short-term antibiotic use (aOR 4.2, P=0.02), suggesting microbiome disruption.
Conclusions:
- High iGBS risk in multiples and recurrent cases points to disturbed individual microbiomes and potential failures in GBS strain integration.
- Identical GBS serotypes in recurrent/multiple infections suggest a common source or failed colonization resistance.
- Fluctuations in host immunity and individual exposure patterns likely contribute to the failure of natural niche occupation by GBS.
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