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Updated: Jan 24, 2026

A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting
Published on: January 12, 2018
The vaginal microbiome and preterm birth
Jennifer M Fettweis1,2,3, Myrna G Serrano1,3, J Paul Brooks3,4
1Department of Microbiology and Immunology, School of Medicine, Virginia Commonwealth University, Richmond, VA, USA.
Insights
Preterm birth risk is higher in women of African ancestry. Vaginal microbiome analysis revealed specific bacteria linked to preterm delivery, offering new ways to assess risk.
Area of Science:
- Microbiome research
- Reproductive health
- Genomics
Background:
- Preterm birth affects over 10% globally, with disproportionate rates among women of African ancestry in the US.
- Understanding the factors contributing to preterm birth disparities is crucial for public health.
Purpose of the Study:
- To identify microbial and host factors associated with preterm birth in a cohort of women of African ancestry.
- To leverage multi-omics data for novel preterm birth risk assessment.
Main Methods:
- Longitudinal analysis of 16S ribosomal RNA, metagenomic, metatranscriptomic, and cytokine data from 45 preterm and 90 term birth controls.
- Characterization of vaginal microbiome composition and function.
- Correlation analysis between microbial taxa and host inflammatory markers.
Main Results:
- Significant differences in vaginal microbial communities were observed between preterm and term birth groups.
- Lower levels of Lactobacillus crispatus and higher levels of specific bacteria (e.g., BVAB1, Sneathia amnii, Prevotella) were associated with preterm birth.
- Preterm-associated taxa correlated with increased proinflammatory cytokines in vaginal fluid.
Conclusions:
- Specific vaginal microbial taxa and host inflammatory profiles serve as potential biomarkers for preterm birth risk.
- These findings open new avenues for developing targeted interventions and risk assessment strategies for preterm birth.
Abstract:
The incidence of preterm birth exceeds 10% worldwide. There are significant disparities in the frequency of preterm birth among populations within countries, and women of African ancestry disproportionately bear the burden of risk in the United States. In the present study, we report a community resource that includes 'omics' data from approximately 12,000 samples as part of the integrative Human Microbiome Project. Longitudinal analyses of 16S ribosomal RNA, metagenomic, metatranscriptomic and cytokine profiles from 45 preterm and 90 term birth controls identified harbingers of preterm birth in this cohort of women predominantly of African ancestry. Women who delivered preterm exhibited significantly lower vaginal levels of Lactobacillus crispatus and higher levels of BVAB1, Sneathia amnii, TM7-H1, a group of Prevotella species and nine additional taxa. The first representative genomes of BVAB1 and TM7-H1 are described. Preterm-birth-associated taxa were correlated with proinflammatory cytokines in vaginal fluid. These findings highlight new opportunities for assessment of the risk of preterm birth.
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