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Published on: August 1, 2019
Inactivation of M111 Protein Gene Modifies Streptococcus Pyogenes Interactions with Mouse Macrophages In Vitro
M A Suvorova1, T A Kramskaya2, A N Suvorov2
1Institute of Experimental Medicine, St. Petersburg, Russia. maria_suvorova@mail.ru.
Abstract:
Immunomodulatory properties of S. pyogenes protein M111 were studied on the model of Gurov strain and its isogenic mutant not expressing M protein. Mouse resident peritoneal macrophages were incubated with bacteria and generation of nitroxide and superoxide anions and production of IL-6, IL-10, and IL-17 were evaluated. Protein M111 modified macrophage response: it exhibited antiphagocytic activity, prevented ROS formation, and stimulated the production of anti-inflammatory cytokine IL-10. The results suggested that this protein could serve in the bacteria as a factor suppressing the host defense forces and promoting the realization of the strategy beneficial for pathogens - escape from the host immune defense.
Insights
Streptococcus pyogenes protein M111 suppresses host immune defenses by inhibiting macrophage responses and promoting bacterial evasion. This protein prevents reactive oxygen species (ROS) generation and stimulates anti-inflammatory cytokine IL-10 production.
Area of Science:
- Microbiology
- Immunology
- Bacterial Pathogenesis
Background:
- Streptococcus pyogenes utilizes various virulence factors to evade host immune responses.
- Protein M is a key surface protein in S. pyogenes, known for its role in pathogenesis.
Purpose of the Study:
- To investigate the immunomodulatory effects of S. pyogenes protein M111 on macrophage function.
- To determine how protein M111 influences the host's innate immune response to bacterial infection.
Main Methods:
- Incubation of mouse resident peritoneal macrophages with S. pyogenes Gurov strain and its isogenic M protein mutant.
- Quantification of reactive oxygen species (ROS) including nitroxide and superoxide anions.
- Measurement of cytokine production, specifically IL-6, IL-10, and IL-17.
Main Results:
- Protein M111 demonstrated antiphagocytic activity, hindering macrophage engulfment of bacteria.
- M111 prevented the formation of reactive oxygen species (ROS) by macrophages.
- The presence of M111 significantly stimulated the production of the anti-inflammatory cytokine IL-10.
Conclusions:
- S. pyogenes protein M111 acts as a virulence factor by modulating macrophage activity.
- This protein contributes to bacterial immune evasion by suppressing key host defense mechanisms.
- Protein M111 facilitates pathogen survival by dampening the inflammatory response and promoting escape from immune surveillance.
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