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Updated: Sep 25, 2025

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Group B streptococcus infection during pregnancy and infancy: estimates of regional and global burden
Bronner P Gonçalves1, Simon R Procter1, Proma Paul1
1Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK; Maternal, Adolescent, Reproductive & Child Health Centre, London School of Hygiene & Tropical Medicine, London, UK.
Insights
Group B Strep (GBS) during pregnancy causes infant infections, stillbirths, and maternal issues. This study estimates the global burden of GBS, including neurodevelopmental impairment in infants surviving invasive GBS disease.
Area of Science:
- Obstetrics and Gynecology
- Neonatology
- Infectious Diseases
- Global Health Epidemiology
Background:
- Group B Streptococcus (GBS) is a significant cause of invasive GBS disease (iGBS) in infants, leading to meningitis, sepsis, stillbirths, maternal infections, and preterm births.
- Existing data on the neurodevelopmental impairment (NDI) following iGBS, particularly sepsis, is limited, necessitating updated global estimates.
- This study addresses critical data gaps concerning the full spectrum of GBS-related adverse outcomes in pregnancy and infancy.
Purpose of the Study:
- To estimate the global burden of maternal GBS colonization and invasive GBS disease (iGBS) in infants and mothers for the year 2020.
- To quantify the incidence of NDI among children surviving iGBS and the proportion of stillbirths associated with GBS.
- To assess the association between GBS colonization and preterm births.
Main Methods:
- A meta-analysis of existing systematic reviews and recent multicountry studies was conducted using Bayesian hierarchical models.
- Data from 183 countries were used to estimate maternal GBS colonization, infant iGBS cases and deaths, maternal iGBS cases, and GBS-associated stillbirths.
- Calculations included excess preterm births linked to maternal GBS colonization, applying UN-estimated stillbirth risks.
Main Results:
- An estimated 19.7 million pregnant women had GBS colonization in 2020.
- Approximately 231,800 early-onset and 162,200 late-onset infant iGBS cases were estimated.
- An estimated 37,100 children surviving iGBS were predicted to develop moderate to severe NDI, alongside 46,200 GBS-associated stillbirths.
Conclusions:
- This comprehensive assessment highlights the substantial global burden of pregnancy-related GBS, encompassing both acute and long-term consequences.
- The findings underscore the public health importance of investing in maternal GBS immunization and other preventive strategies.
- Accurate estimation of GBS burden, including NDI and preterm births, is crucial for informing global health policies and interventions.
Background:
Group B streptococcus (GBS) colonisation during pregnancy can lead to invasive GBS disease (iGBS) in infants, including meningitis or sepsis, with a high mortality risk. Other outcomes include stillbirths, maternal infections, and prematurity. There are data gaps, notably regarding neurodevelopmental impairment (NDI), especially after iGBS sepsis, which have limited previous global estimates. In this study, we aimed to address this gap using newly available multicountry datasets.
Methods:
We collated and meta-analysed summary data, primarily identified in a series of systematic reviews published in 2017 but also from recent studies on NDI and stillbirths, using Bayesian hierarchical models, and estimated the burden for 183 countries in 2020 regarding: maternal GBS colonisation, iGBS cases and deaths in infants younger than 3 months, children surviving iGBS affected by NDI, and maternal iGBS cases. We analysed the proportion of stillbirths with GBS and applied this to the UN-estimated stillbirth risk per country. Excess preterm births associated with maternal GBS colonisation were calculated using meta-analysis and national preterm birth rates.
Findings:
Data from the seven systematic reviews, published in 2017, that informed the previous burden estimation (a total of 515 data points) were combined with new data (17 data points) from large multicountry studies on neurodevelopmental impairment (two studies) and stillbirths (one study). A posterior median of 19·7 million (95% posterior interval 17·9-21·9) pregnant women were estimated to have rectovaginal colonisation with GBS in 2020. 231 800 (114 100-455 000) early-onset and 162 200 (70 200-394 400) late-onset infant iGBS cases were estimated to have occurred. In an analysis assuming a higher case fatality rate in the absence of a skilled birth attendant, 91 900 (44 800-187 800) iGBS infant deaths were estimated; in an analysis without this assumption, 58 300 (26 500-125 800) infant deaths from iGBS were estimated. 37 100 children who recovered from iGBS (14 600-96 200) were predicted to develop moderate or severe NDI. 40 500 (21 500-66 200) maternal iGBS cases and 46 200 (20 300-111 300) GBS stillbirths were predicted in 2020. GBS colonisation was also estimated to be potentially associated with considerable numbers of preterm births.
Interpretation:
Our analysis provides a comprehensive assessment of the pregnancy-related GBS burden. The Bayesian approach enabled coherent propagation of uncertainty, which is considerable, notably regarding GBS-associated preterm births. Our findings on both the acute and long-term consequences of iGBS have public health implications for understanding the value of investment in maternal GBS immunisation and other preventive strategies.
Funding:
Bill & Melinda Gates Foundation.
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