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A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
A Review of Early- and Late-Onset Neonatal Infections by Group B Streptococcus: Pathophysiology and Vaccine Prospects
Wahid Hanan Hamimi1, Hajar Ahmad Jamil1, Danesh Anamulai1
1Department of Basic Medical Sciences, Kulliyyah of Medicine, International Islamic University, Pahang, Malaysia.
Insights
Group B Streptococcus (GBS) causes significant neonatal illness and death. A maternal GBS vaccine is urgently needed to prevent invasive GBS disease, as current prevention methods are insufficient.
Area of Science:
- Obstetrics and Gynecology
- Neonatal Medicine
- Infectious Diseases
Background:
- Group B Streptococcus (GBS) is a major cause of neonatal morbidity and mortality globally.
- Vaginal GBS colonization in pregnant women can lead to invasive GBS (iGBS) disease in newborns.
- Current prevention strategies like intrapartum antibiotic prophylaxis (IAP) have limitations, especially in low-resource settings.
Purpose of the Study:
- To review the mechanisms of GBS virulence and host interactions in invasive GBS disease.
- To highlight the need for a maternal GBS vaccine.
- To inform vaccine design and therapeutic development.
Main Methods:
- This review synthesizes existing literature on GBS pathogenesis.
- It examines the interplay between GBS virulence factors and host responses.
- The review discusses the limitations of current GBS prevention strategies.
Main Results:
- GBS virulence factors and host interactions are critical in causing invasive GBS disease.
- Early-onset disease (EOD) is often sepsis, while late-onset disease (LOD) is frequently meningitis.
- IAP reduces EOD but not LOD and faces implementation challenges in LMICs.
Conclusions:
- A safe, effective, and affordable maternal GBS vaccine is essential.
- Understanding GBS-host interactions is key for developing new vaccines and therapies.
- Improved GBS prevention is crucial to reduce neonatal mortality and morbidity worldwide.
Abstract:
Group B Streptococcus (GBS) remains a leading cause of neonatal morbidity and mortality worldwide. About 18% of pregnant women are colonized in the gastrointestinal or genitourinary tracts. Vaginal colonization can result in ascending intrauterine infection, enabling GBS to reach the amniotic fluid and infect the fetus during pregnancy or the newborn at delivery, leading to invasive GBS (iGBS) disease. Early-onset disease (EOD) typically manifests as sepsis, whereas late-onset disease (LOD) is more often associated with meningitis. Intrapartum antibiotic prophylaxis (IAP), based on screening at 36-37 weeks' gestation, has substantially reduced EOD but not LOD, and implementation remains difficult in low- and middle-income countries (LMICs) with limited resources. This underscores the urgent need for a safe, effective, and affordable maternal GBS vaccine. This review examines how GBS virulence factors interact with host factors, causing iGBS. Understanding these mechanisms is essential for vaccine design and therapeutic development.
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