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Updated: Aug 23, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Laboratory detection of group B Streptococcus for prevention of perinatal disease
1Centre de Recherche en Infectiologie de l'Université Laval, Centre Hospitalier Universitaire de Québec (Pavillon CHUL), 2705 Boulevard Laurier, Ainte-Foy, QC, Canada.
Insights
Group B Streptococcus (GBS) causes serious neonatal infections. Rapid real-time PCR assays improve GBS screening accuracy in pregnant women, aiding prevention of infant GBS disease.
Area of Science:
- Microbiology
- Infectious Diseases
- Obstetrics
Background:
- Group B Streptococcus (GBS) is a leading cause of neonatal morbidity and mortality.
- Despite prevention efforts, GBS remains a significant threat to newborns, causing sepsis and meningitis.
- The gastrointestinal tract is the primary reservoir for GBS, leading to vaginal colonization in women.
Purpose of the Study:
- To review laboratory methods for GBS detection in pregnant women.
- To discuss the impact of GBS detection on preventing neonatal infections.
- To evaluate the role of GBS screening in rationalizing antibiotic use.
Main Methods:
- Analysis of various laboratory methods for GBS detection.
- Comparison of standard culture-based methods with newer molecular assays.
- Review of clinical samples from pregnant women, specifically vagino-rectal samples.
Main Results:
- Real-time polymerase chain reaction (PCR) assays offer rapid and highly sensitive GBS detection.
- FDA-approved real-time PCR assays improve accuracy and speed of GBS colonization screening.
- Molecular assays show advantages over traditional culture-based methods for GBS detection.
Conclusions:
- Newer molecular methods, like real-time PCR, enhance GBS screening in pregnant women.
- Improved GBS detection aids in preventing neonatal GBS infections.
- Accurate and rapid GBS screening supports judicious antibiotic use.
Abstract:
Group B Streptococcus (GBS) or Streptococcus agalactiae emerged in the 1970s as the leading cause of neonatal morbidity and mortality. Today, GBS remains one of the leading causes of sepsis and meningitis in newborns despite important prevention efforts, including the issuance of recommendations for prevention of perinatal GBS disease by the American College of Obstetricians and Gynecologists, the Centers for Disease Control and Prevention, and the American Academy of Pediatrics in 1996/1997. The gastrointestinal tract is the natural human reservoir for GBS and is the likely source of vaginal colonization. GBS disease in newborns usually results from ascending spread of GBS into the amniotic fluid, which leads to neonatal colonization and to invasive disease in some infants. This review analyzes the various laboratory methods available for the detection of GBS from clinical samples collected from pregnant women and will discuss their impact in the prevention of neonatal GBS infections and in the rationalization of antibiotic use. The recent commercial availability of a rapid and highly sensitive real-time polymerase chain reaction assay suitable for the specific detection of GBS from vagino-rectal samples obtained from pregnant women during delivery, which is approved by the US Food and Drug Administration, provides improvements in the accuracy and rapidity of GBS colonization screening compared to the standard culture-based method using the recommended selective enrichment broth.
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