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Updated: Aug 5, 2025

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Interspecies Interactions within the Host: the Social Network of Group B Streptococcus
Marlyd E Mejia1, Clare M Robertson1, Kathryn A Patras1,2
1Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
Insights
Group B Streptococcus (GBS) causes significant neonatal deaths. Understanding GBS interactions with other microbes is key to developing new therapies beyond antibiotics to prevent GBS disease.
Area of Science:
- Microbiology
- Neonatal Health
- Microbial Ecology
Background:
- Group B Streptococcus (GBS) is a major cause of neonatal mortality and stillbirths.
- GBS colonizes maternal mucosal surfaces, leading to vertical transmission.
- Current antibiotic prophylaxis for GBS has limitations, including altered neonatal microbiota and unaffected late-onset disease incidence.
Purpose of the Study:
- To review current knowledge on GBS interactions with other microbes.
- To explore GBS's role in the developing neonatal microbiota.
- To identify potential targets for novel GBS disease prevention strategies.
Main Methods:
- Literature review encompassing clinical studies, agricultural/aquaculture observations, and animal models.
- Analysis of in vitro findings on GBS interactions with commensal and pathogenic microbes.
- Inclusion of new animal models for GBS colonization and infection.
Main Results:
- GBS interactions with other microbes are complex and occur at mucosal surfaces.
- Antibiotic use for GBS prophylaxis has unintended consequences on the neonatal microbiome.
- Emerging evidence suggests GBS-microbe interactions influence neonatal disease pathogenesis.
Conclusions:
- Further research into GBS-microbe interactions is crucial for understanding neonatal disease.
- Novel therapeutic strategies, such as prebiotics and probiotics, show promise for GBS prevention.
- Targeting microbial interactions offers a potential alternative to broad-spectrum antibiotics.
Abstract:
Group B Streptococcus (GBS) is a pervasive neonatal pathogen accounting for a combined half a million deaths and stillbirths annually. The most common source of fetal or neonatal GBS exposure is the maternal microbiota. GBS asymptomatically colonizes the gastrointestinal and vaginal mucosa of 1 in 5 individuals globally, although its precise role in these niches is not well understood. To prevent vertical transmission, broad-spectrum antibiotics are administered to GBS-positive mothers during labor in many countries. Although antibiotics have significantly reduced GBS early-onset neonatal disease, there are several unintended consequences, including an altered neonatal microbiota and increased risk for other microbial infections. Additionally, the incidence of late-onset GBS neonatal disease remains unaffected and has sparked an emerging hypothesis that GBS-microbe interactions in developing neonatal gut microbiota may be directly involved in this disease process. This review summarizes our current understanding of GBS interactions with other resident microbes at the mucosal surface from multiple angles, including clinical association studies, agriculture and aquaculture observations, and experimental animal model systems. We also include a comprehensive review of in vitro findings of GBS interactions with other bacterial and fungal microbes, both commensal and pathogenic, along with newly established animal models of GBS vaginal colonization and in utero or neonatal infection. Finally, we provide a perspective on emerging areas of research and current strategies to design microbe-targeting prebiotic or probiotic therapeutic intervention strategies to prevent GBS disease in vulnerable populations.
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