Abstract
Toxoplasma gondii is a wide spread pathogen that can cause severe and even fatal disease in fetuses and immune-compromised hosts. As an obligate intracellular parasite, Toxoplasma must alter the environment of its host cell in order to establish its replicative niche. This is accomplished, in part, by secretion of factors into the host cell that act to modulate processes such as transcription. Previous studies demonstrated that genes encoding transcription factors such as c-jun, junB, EGR1, and EGR2 were amongst the host genes that were the most rapidly upregulated following infection. In cells stimulated with growth factors, these genes are regulated by a transcription factor named Serum Response Factor. Serum Response Factor is a ubiquitously expressed DNA binding protein that regulates growth and actin cytoskeleton genes via MAP kinase or actin cytoskeletal signaling, respectively. Here, we report that Toxoplasma infection leads to the rapid activation of Serum Response Factor. Serum Response Factor activation is a Toxoplasma-specific event since the transcription factor is not activated by the closely related protozoan parasite, Neospora caninum. We further demonstrate that Serum Response Factor activation requires a parasite-derived secreted factor that signals via host MAP kinases but independently of the host actin cytoskeleton. Together, these data define Serum Response Factor as a host cell transcription factor that regulates immediate early gene expression in Toxoplasma-infected cells.
Highlights
Toxoplasma gondii is an obligate intracellular protozoan parasite that is an important pathogen of fetuses and immune-compromised patients [1,2]
Toxoplasma Infection Activates Serum Response Factor (SRF) We previously showed that Toxoplasma rapidly activates the host cell transcription factors EGR and AP-1 via upregulation of their mRNAs [24]
Because SRF is an important regulator of EGR and AP-1 transcription in growth-factor stimulated cells, experiments were undertaken to test whether Toxoplasma uses SRF to activate AP-1 and EGR
Summary
Toxoplasma gondii is an obligate intracellular protozoan parasite that is an important pathogen of fetuses and immune-compromised patients [1,2]. We and others have used transcriptional profiling assays as an approach to identify host cell pathways important for Toxoplasma growth [10,11,12]. These studies demonstrated that infection leads to upregulation of genes at both early (within 2 hpi) and late time points following infection. While many of the early genes encode proteins involved in host immune responses, others including cjun, junB, c-myc, EGR1, and EGR2 were upregulated These genes, which are well known immediate early response genes in growth factor-stimulated cells, encode transcription factors that regulate cell survival and growth genes [13,14]. The rapid responsiveness of these genes to growth factor stimulation is due to serum response elements (SREs) in the promoters of these genes [15]
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