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A Simple Fluorescence Assay for Quantification of Canine Neutrophil Extracellular Trap Release
Published on: November 21, 2016
Extracellular Traps Released by Neutrophils from Cats are Detrimental to Toxoplasma gondii Infectivity
Isabela S Macedo1, Marcos V A Lima1, Jéssica S Souza1
1Laboratório de Biologia Estrutural, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro 21040-360, RJ, Brazil.
Insights
Cats combat Toxoplasma gondii infection by releasing neutrophil extracellular traps (NETs). This study reveals how cat neutrophils produce NETs to kill the parasite, a conserved immune defense across hosts.
Area of Science:
- Immunology
- Parasitology
- Veterinary Medicine
Background:
- Toxoplasma gondii causes toxoplasmosis, a widespread disease affecting over 30% of humans.
- Neutrophil extracellular traps (NETs) are part of the innate immune response against T. gondii.
- Mechanisms of NET induction by T. gondii in definitive hosts, like cats, are not well understood.
Purpose of the Study:
- To determine if cat neutrophils produce NETs when stimulated by T. gondii.
- To investigate the underlying mechanisms of T. gondii-induced NET formation in cats.
Main Methods:
- Stimulation of cat neutrophils with T. gondii tachyzoites.
- Quantification of NET-derived DNA, and detection of histone H1 and myeloperoxidase.
- Inhibition assays targeting elastase, intracellular calcium, and PI3K-δ; electron microscopy and live imaging.
Main Results:
- Cat neutrophils produced both classical and rapid/early NETs in response to T. gondii.
- NET release was partially inhibited by blocking elastase, intracellular calcium, and PI3K-δ.
- NETs were observed entrapping and killing T. gondii tachyzoites.
Conclusions:
- Cat neutrophils effectively produce NETs against T. gondii.
- Specific pathways involving elastase, calcium, and PI3K-δ contribute to NET formation.
- NET production is a conserved host defense mechanism against T. gondii across different host types.
Abstract:
Toxoplasma gondii is the causative agent of toxoplasmosis, an infectious disease that affects over 30% of the human world population, causing fatal infections in immunocompromised individuals and neonates. The life cycle of T. gondii is complex, and involves intermediate hosts (birds and mammals) and definitive hosts (felines, including domestic cats). The innate immune repertoire against the parasite involves the production of neutrophil extracellular traps (NET), and neutrophils from several intermediate hosts produce NET induced by T. gondii. However, the mechanisms underlying NET release in response to the parasite have been poorly explored. Therefore, the aims of this study were to investigate whether neutrophils from cats produce NET triggered by T. gondii and to understand the mechanisms thereby involved. Neutrophils from cats were stimulated with T. gondii tachyzoites and NET-derived DNA in the supernatant was quantified during the time. The presence of histone H1 and myeloperoxidase was detected by immunofluorescence. We observed that cat neutrophils produce both classical and rapid/early NET stimulated by T. gondii. Inhibition of elastase, intracellular calcium, and phosphatidylinositol 3-kinase (PI3K)-δ partially blocked classical NET release in response to the parasite. Electron microscopy revealed strands and networks of DNA in close contact or completely entrapping parasites. Live imaging showed that tachyzoites are killed by NET. We conclude that the production of NET is a conserved strategy to control infection by T. gondii amongst intermediate and definitive hosts.
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