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Published on: October 18, 2019
Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation
Masaya Takehara1, Teruhisa Takagishi1, Soshi Seike1
1Department of Microbiology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-cho, Tokushima 770-8514, Japan.
Abstract:
Although granulopoiesis is accelerated to suppress bacteria during infection, some bacteria can still cause life-threatening infections, but the mechanism behind this remains unclear. In this study, we found that mature neutrophils in bone marrow cells (BMCs) were decreased in C. perfringens-infected mice and also after injection of virulence factor α-toxin. C. perfringens infection interfered with the replenishment of mature neutrophils in the peripheral circulation and the accumulation of neutrophils at C. perfringens-infected sites in an α-toxin-dependent manner. Measurements of bacterial colony-forming units in C. perfringens-infected muscle revealed that α-toxin inhibited a reduction in the load of C. perfringens. In vitro treatment of isolated BMCs with α-toxin (phospholipase C) revealed that α-toxin directly decreased mature neutrophils. α-Toxin did not influence the viability of isolated mature neutrophils, while simultaneous treatment of BMCs with granulocyte colony-stimulating factor attenuated the reduction of mature neutrophils by α-toxin. Together, our results illustrate that impairment of the innate immune system by the inhibition of neutrophil differentiation is crucial for the pathogenesis of C. perfringens to promote disease to a life-threatening infection, which provides new insight to understand how pathogenic bacteria evade the host immune system.
Insights
Clostridium perfringens alpha-toxin impairs neutrophil production, hindering the immune response and promoting severe infections. This bacterial toxin disrupts neutrophil differentiation, contributing to life-threatening outcomes.
Area of Science:
- Immunology
- Microbiology
- Pathogenesis
Background:
- Bacterial infections can cause life-threatening disease despite accelerated granulopoiesis.
- The mechanisms by which some bacteria overcome host immune defenses remain incompletely understood.
Purpose of the Study:
- To investigate the role of Clostridium perfringens alpha-toxin in neutrophil dynamics during infection.
- To elucidate how C. perfringens evades the host immune system.
Main Methods:
- Assessing neutrophil counts in C. perfringens-infected mice and after alpha-toxin administration.
- In vitro experiments using bone marrow cells (BMCs) treated with alpha-toxin and granulocyte colony-stimulating factor.
- Measuring bacterial load in infected muscle tissue.
Main Results:
- C. perfringens infection and alpha-toxin decreased mature neutrophils in bone marrow cells (BMCs).
- Alpha-toxin interfered with neutrophil replenishment and accumulation at infection sites.
- Alpha-toxin inhibited bacterial clearance and promoted bacterial load in vivo.
- In vitro, alpha-toxin directly reduced mature neutrophils without affecting their viability.
Conclusions:
- Impaired neutrophil differentiation by alpha-toxin is critical for C. perfringens pathogenesis.
- This mechanism allows pathogenic bacteria to evade innate immunity and cause severe infections.
- Findings offer new insights into bacterial evasion strategies and host-pathogen interactions.
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