Publications by authors named "T C Paredes-Santos"

is an intracellular parasite that can activate the NLRP1 inflammasome leading to macrophage pyroptosis in Lewis rats, but the underlying mechanism is not well understood. In this study, we performed a genome-wide CRISPR screen and identified the dense granule proteins GRA35, GRA42, and GRA43 as the effectors mediating cell death in Lewis rat macrophages. GRA35 localizes on the parasitophorous vacuole membrane, where it interacts with the host E3 ubiquitin ligase ITCH.

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Article Synopsis
  • An intracellular parasite can trigger a specific immune response (pyroptosis) in Lewis rat macrophages via the NLRP1 inflammasome, but the mechanism is not fully understood.
  • A genome-wide CRISPR screen identified dense granule proteins GRA35, GRA42, and GRA43 as key players in this cell death process.
  • The interaction between GRA35 and the host E3 ubiquitin ligase ITCH is crucial, affecting immune response and fitness in activated human cells, highlighting ITCH's role in the immune response to intracellular infections.
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Toxoplasma gondii is a parasite that replicates within a specialized compartment called the parasitophorous vacuole (PV), which is surrounded by the PV membrane (PVM). To obtain essential nutrients, Toxoplasma must transport molecules across the PVM, a process mediated by the secreted parasite proteins GRA17 and GRA23. These proteins form pores in the PVM through which small molecules can diffuse in and out of the PV.

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virulence depends on its ability to evade or survive the toxoplasmacidal mechanisms induced by interferon gamma (IFNγ). While many genes involved in the evasion of the murine IFNγ response have been identified, genes required to survive the human IFNγ response are largely unknown. In this study, we used a genome-wide loss-of-function screen to identify genes important for parasite fitness in IFNγ-stimulated primary human fibroblasts.

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Macrophages play an essential role in the early immune response against Toxoplasma and are the cell type preferentially infected by the parasite in vivo. Interferon gamma (IFNγ) elicits a variety of anti-Toxoplasma activities in macrophages. Using a genome-wide CRISPR screen we identify 353 Toxoplasma genes that determine parasite fitness in naїve or IFNγ-activated murine macrophages, seven of which are further confirmed.

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