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Updated: Jul 13, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Group B streptococcal infections in the postgenomic era
Insights
Group B streptococci (GBS) invade host cells, causing neonatal infections. Research uses molecular methods to understand GBS virulence and develop new treatments for bacterial pneumonia.
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Molecular Pathogenesis
Background:
- Group B streptococci (GBS) invade eukaryotic cells, a key mechanism for neonatal disease.
- Research focuses on molecular virulence factors of Gram-positive bacteria, including GBS.
Discussion:
- Investigating GBS cell entry, immune evasion (complement inhibition, phagocytosis resistance), and survival in host environments.
- Utilizing genetic techniques to identify GBS virulence genes and biosynthetic pathways for capsular polysaccharide.
- Exploring host-pathogen interactions in bacterial pneumonia using Staphylococcus aureus and advanced genomic/proteomic methods.
Key Insights:
- Molecular approaches reveal GBS virulence mechanisms and genetic basis for traits like cell invasion.
- Understanding GBS pathogenesis is crucial for combating neonatal infections.
Outlook:
- Characterizing bacterial persistence mechanisms in lung infections.
- Identifying host airway proteins involved in innate immunity against bacterial pneumonia.
Abstract:
Dr Rubens is a pediatric infectious disease specialist and microbiologist, with a longstanding interest in the molecular pathogenesis of bacterial perinatal infections by Gram-positive bacteria. Group B streptococci (GBS) have been shown to invade eukaryotic cells and this process may be the main mechanism used by the organism to cause disease in neonates. Molecular approaches are used to identify the genetic and biochemical basis of specific virulence traits, such as epithelial/endothelial cell entry and transcytosis, evasion of innate immune mechanisms by inhibiting complement activation and phagocytic uptake, and microbial survival in various host environments (bloodstream, reproductive system and neonatal lung). Hence, these projects apply to both in vitro and in vivo model systems. Genetic techniques are also utilized to identify the genes and biosynthetic mechanisms important for the production of capsular polysaccharide and other virulence traits by GBS. Recently, Dr Rubens's group has started a project characterizing the early stages of bacterial pneumonia by investigating the host:pathogen interaction after introducing Staphylococcus aureus into the airway using genomic and proteomic techniques. This project will eventually characterize the bacterial response to the lung airway, including specific traits critical for microbial persistence in the face of lung innate immunity. They have also begun to characterize the host airway proteome for the proteins that contribute to innate immune mechanisms.
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