Clostridium perfringens Phospholipase C, an Archetypal Bacterial Virulence Factor, induces the Formation of Extracellular Traps by Human Neutrophils

 

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Autores: Badilla Vargas, Lisa, Pereira Reyes, Reinaldo, Molina Mora, José Arturo, Alape Girón, Alberto, Flores Díaz, Marietta
Formato: artículo preliminar
Fecha de Publicación:2023
Descripción:Neutrophil extracellular traps (NETs) are networks of DNA and various microbicidal proteins, released to the extracellular space to kill invading microorganisms and prevent their dissemination. However, a NETs excess is detrimental to the host and is involved in the pathogenesis of various inflammatory and immunothrombotic diseases. Clostridium perfringens is a widely distributed pathogen that produces many exotoxins associated with various animal and human diseases, including the necrotizing soft tissue infection called gas gangrene. This work demonstrates that the C. perfringens toxinotype A secretome induces NETs formation (NETosis) in human neutrophils. Antibodies against the C. perfringens phospholipase C (CpPLC) completely abrogate the NETosis-inducing activity of that secretome, and the recombinant CpPLC induces NETs formation in a dose-response manner. Proteomic analysis of the C. perfringens secretome identified 40 proteins, including a DNAse and two 5´-nucleotidases homologous to virulence factors that help other pathogens evade NETs. CpPLC induces suicidal NETosis through a mechanism that requires calcium release from inositol trisphosphate receptor (IP3) sensitive stores, activation of protein kinase C (PKC), and the mitogen-activated protein kinase/ extracellular signal-regulated kinase (MEK/ERK) pathways, and the production of reactive oxygen species (ROS) by the xanthine oxidase (XO) and the metabolism of arachidonic acid. CpPLC was the first bacterial toxin found to be enzymatically active and is the major virulence factor in the pathogenesis of gas gangrene. This toxin drives the formation of neutrophil/platelet aggregates within the vasculature of the infected tissues, which leads to the circulation's halt and extends the anaerobic environment for C. perfringens growth. It is suggested that this pathogen benefits from having access to the metabolic resources of the tissue injured by a dysregulated intravascular NETosis, and then escapes and spreads to deeper tissues. Understanding the role of NETs in the thrombotic events occurring in gas gangrene could help develop novel therapeutic strategies to reduce mortality, improve muscle regeneration, and prevent deleterious patient outcomes.
País:Kérwá
Institución:Universidad de Costa Rica
Repositorio:Kérwá
Lenguaje:Inglés
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/89483
Acceso en línea:https://hdl.handle.net/10669/89483
Palabra clave:Anaerobes
Clostridium perfringens
Secretome
Proteomic analysis
Bacterial Toxins
exotoxin
Clostridium toxins
phospholipase C
bacterial pathogenesis
innate immunity
neutrophils
NETs
NETosis
ROS
antioxidants
gas gangrene