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Updated: Feb 24, 2026

Invasion of Human Cells by a Bacterial Pathogen
Published on: March 21, 2011
Streptococcus pyogenes translocates across an epithelial barrier
1Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry.
Abstract:
Streptococcus pyogenes is a β-hemolytic organism responsible for a wide variety of human diseases that commonly occur as self-limiting purulent diseases of the pharynx and skin. Although the occurrence of invasive infections by S. pyogenes is rare, mortality rates remain high even with progressive medical therapy. As a prerequisite for causing the severe invasive disease, S. pyogenes must invade underlying sterile tissues by translocating across the epithelial barrier. In this study, streptolysin S and SpeB were identified as the novel factors that facilitate bacterial translocation via degradation of intercellular junctions. Furthermore, we found that S. pyogenes exploits host plasminogen for acceleration of bacterial invasion into deeper tissues via tricellular tight junctions. Here, I would like to show our study on bacterial translocation across the epithelial barrier through paracellular route.
Insights
Streptococcus pyogenes invades tissues by degrading cell junctions using streptolysin S and SpeB. The bacteria also use host plasminogen to speed up invasion through tricellular tight junctions.
Area of Science:
- Microbiology
- Cell Biology
- Infectious Diseases
Background:
- Streptococcus pyogenes causes pharyngeal and skin infections.
- Invasive S. pyogenes infections are rare but have high mortality.
- Bacterial translocation across epithelial barriers is crucial for invasive disease.
Purpose of the Study:
- To identify factors enabling Streptococcus pyogenes translocation across epithelial barriers.
- To elucidate the mechanisms of bacterial invasion into deeper tissues.
Main Methods:
- Investigated bacterial translocation mechanisms of Streptococcus pyogenes.
- Identified bacterial factors and host interactions facilitating invasion.
Main Results:
- Streptolysin S and SpeB facilitate bacterial translocation by degrading intercellular junctions.
- S. pyogenes exploits host plasminogen to accelerate invasion via tricellular tight junctions.
Conclusions:
- Novel factors, streptolysin S and SpeB, enable S. pyogenes epithelial barrier translocation.
- Host plasminogen is exploited by S. pyogenes to enhance invasion through tricellular tight junctions.
- Understanding these mechanisms is key to combating invasive streptococcal infections.
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