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Implementation of a Permeable Membrane Insert-based Infection System to Study the Effects of Secreted Bacterial Toxins on Mammalian Host Cells
Published on: August 19, 2016
M type 1 and 3 group A streptococci stimulate tissue factor-mediated procoagulant activity in human monocytes and
A E Bryant1, S M Hayes-Schroer, D L Stevens
1Veterans Affairs Medical Center, 500 West Fort Street, Building 45, Boise, Idaho 83702, USA. abryant@mindspring.com
Abstract:
Streptococcal toxic shock syndrome (StrepTSS) is an invasive infection characterized by marked coagulopathy, multiple organ failure, and rapid tissue destruction and is strongly associated with M type 1 and 3 group A streptococci (GAS). Initiation of the coagulation cascade with formation of microvascular thrombi contributes to multiple organ failure in human cases of gram-negative bacteremia; however, little is known regarding the mechanism of coagulopathy in StrepTSS. Thus, we investigated the abilities of several strains of M type 1 and 3 GAS isolated from human cases of StrepTSS to stimulate production of tissue factor (TF), the principal initiator of coagulation in vivo. Washed, killed M type 1 and 3 GAS, but not M type 6 GAS, elicited high-level TF-mediated procoagulant activity from both isolated human monocytes and cultured human umbilical vein endothelial cells. M type 1 GAS consistently elicited higher levels of TF from monocytes than did M type 3 GAS. GAS-induced TF synthesis in monocytes did not correlate with production of tumor necrosis factor alpha or interleukin-8. Conversely, M type 3 GAS were consistently more potent than M type 1 GAS in stimulating endothelial cell TF synthesis. These results demonstrate that (i) M type 1 and 3 strains of GAS are potent inducers of TF synthesis, (ii) GAS-induced TF synthesis is not simply an epiphenomenon of cytokine generation, and (iii) induction of TF in endothelial cells and monocytes may be M type specific. In total, these findings suggest that a novel interaction between GAS and host cells contributes to the observed coagulopathy in StrepTSS.
Insights
Group A Streptococcus (GAS) M type 1 and 3 strains trigger tissue factor (TF) production, a key factor in blood clotting. This study reveals a specific mechanism contributing to coagulopathy in Streptococcal toxic shock syndrome (StrepTSS).
Area of Science:
- Microbiology
- Immunology
- Hematology
Background:
- Streptococcal toxic shock syndrome (StrepTSS) involves severe coagulopathy and organ failure, often linked to M type 1 and 3 Group A Streptococcus (GAS).
- The precise mechanisms driving coagulopathy in StrepTSS remain unclear, particularly the role of coagulation initiation.
Purpose of the Study:
- To investigate the capacity of M type 1 and 3 GAS strains to stimulate tissue factor (TF) production in human monocytes and endothelial cells.
- To elucidate the role of GAS-induced TF in the coagulopathy associated with StrepTSS.
Main Methods:
- Exposure of isolated human monocytes and cultured human umbilical vein endothelial cells to killed M type 1, 3, and 6 GAS strains.
- Measurement of TF-mediated procoagulant activity and TF synthesis.
- Assessment of cytokine production (TNF-α, IL-8) to differentiate TF induction mechanisms.
Main Results:
- M type 1 and 3 GAS potently induced TF synthesis in both monocytes and endothelial cells, unlike M type 6 GAS.
- M type 1 GAS induced higher TF levels in monocytes, while M type 3 GAS were more potent in stimulating endothelial cell TF synthesis.
- GAS-induced TF synthesis was independent of tumor necrosis factor alpha and interleukin-8 production, suggesting a direct pathway.
Conclusions:
- M type 1 and 3 GAS strains are significant inducers of TF, a critical initiator of coagulation.
- GAS-induced TF synthesis is not merely a consequence of general inflammatory cytokine release.
- The M type specificity of TF induction in different host cells suggests a targeted interaction contributing to StrepTSS coagulopathy.
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