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TheToxoplasmaPolymorphic Effector GRA15 Mediates Seizure Induction by Modulating Interleukin-1 Signaling in the Brain
Author(s) -
Taylor Glausen,
Gabriela L. Carrillo,
Richard M Jin,
Jon P. Boyle,
Jeroen P. J. Saeij,
Elizabeth A. Wohlfert,
Michael A. Fox,
Ira J. Blader
Publication year - 2021
Publication title -
mbio
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.562
H-Index - 121
eISSN - 2161-2129
pISSN - 2150-7511
DOI - 10.1128/mbio.01331-21
Subject(s) - toxoplasma gondii , biology , locus (genetics) , gene , immunology , inflammation , epilepsy , encephalitis , effector , signal transduction , genetics , neuroscience , antibody , virus
Toxoplasmic encephalitis can develop in individuals infected with the protozoan parasite Toxoplasma gondii and is typified by parasite replication and inflammation within the brain. Patients often present with seizures, but the parasite genes and host pathways involved in seizure development and/or propagation are unknown. We previously reported that seizure induction in Toxoplasma -infected mice is parasite strain dependent. Using quantitative trait locus mapping, we identify four loci in the Toxoplasma genome that potentially correlate with seizure development. In one locus, we identify the polymorphic virulence factor, GRA15, as a Toxoplasma gene associated with onset of seizures. GRA15 was previously shown to regulate host NF-κB-dependent gene expression during acute infections, and we demonstrate a similar role for GRA15 in brains of toxoplasmic encephalitic mice. GRA15 is important for increased expression of interleukin 1 beta (IL-1β) and other IL-1 pathway host genes, which is significant since IL-1 signaling is involved in onset of seizures. Inhibiting IL-1 receptor signaling reduced seizure severity in Toxoplasma -infected mice. These data reveal one mechanism by which seizures are induced during toxoplasmic encephalitis.

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