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Updated: Feb 16, 2026

Intracranial Subarachnoidal Route of Infection for Investigating Roles of Streptococcus suis Biofilms in Meningitis in a Mouse Infection Model
Published on: July 1, 2018
Binding of Fibronectin to SsPepO Facilitates the Development of Streptococcus suis Meningitis
Feng Liu1,2,3, Jinquan Li1,4, Kang Yan1,2,3
1State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei, China.
Background:
SsPepO is an important virulence in Streptococcus suis.
Methods:
In this study, we showed that SsPepO contributes to the human fibronectin-mediated adherence ability of S. suis to human brain microvascular endothelial cells.
Results:
The addition of an antifibronectin antibody or an arginine-glycine-aspartic acid peptide that blocks fibronectin binding to integrins significantly reduced adherence of the wild-type but not the SspepO mutant strain, indicating the importance of the SsPepO-fibronectin-integrin interaction for S. suis cellular adherence.
Conclusions:
By analyzing Evans blue extravasation in vivo, we showed that the interaction between SsPepO and human fibronectin significantly increased permeability of the blood-brain barrier. Furthermore, the SspepO mutant caused lower bacterial loads in the brain than wild-type S. suis in models of meningitis. These data demonstrate that SsPepO is a fibronectin-binding protein, which plays a contributing role in the development of S. suis meningitis.
Insights
Streptococcus suis SsPepO protein binds human fibronectin, aiding bacterial adherence to brain cells and increasing blood-brain barrier permeability. This interaction is crucial for developing Streptococcus suis meningitis.
Area of Science:
- Microbiology
- Infectious Diseases
- Pathogenesis
Background:
- Streptococcus suis is a significant pathogen causing meningitis.
- SsPepO is identified as a key virulence factor in S. suis infections.
Purpose of the Study:
- To investigate the role of SsPepO in S. suis adherence to human brain microvascular endothelial cells.
- To elucidate the mechanism of SsPepO-mediated pathogenesis, including its interaction with fibronectin and its effect on the blood-brain barrier.
Main Methods:
- Studied the adherence of wild-type and SspepO mutant S. suis strains to endothelial cells.
- Utilized antifibronectin antibodies and integrin-blocking peptides to assess the SsPepO-fibronectin-integrin interaction.
- Analyzed Evans blue extravasation in vivo to evaluate blood-brain barrier permeability.
- Quantified bacterial loads in the brain in a meningitis model.
Main Results:
- SsPepO mediates the adherence of S. suis to human brain microvascular endothelial cells via fibronectin.
- Blocking the fibronectin-integrin interaction significantly reduced adherence of wild-type S. suis but not the SspepO mutant.
- The SsPepO-fibronectin interaction increased blood-brain barrier permeability.
- The SspepO mutant exhibited lower bacterial loads in the brain compared to the wild-type strain.
Conclusions:
- SsPepO is a fibronectin-binding protein essential for S. suis adherence to host cells.
- The SsPepO-fibronectin-integrin pathway is critical for S. suis invasion and pathogenesis.
- SsPepO contributes significantly to the development of Streptococcus suis meningitis.
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