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Ribo-seq of Toxoplasma-infected host cells

ABSTRACT: Ribo-seq of Toxoplasma-infected host cells

PROVIDER: PRJNA533074 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR8907190.fastq.gz	Fastqsanger.gz
	SRR8907200.fastq.gz	Fastqsanger.gz
	SRR8907191.fastq.gz	Fastqsanger.gz
	SRR8907201.fastq.gz	Fastqsanger.gz
	SRR8907192.fastq.gz	Fastqsanger.gz

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Ribo-seq of Toxoplasma-infected host cells

Project description:Toxoplasma gondii is a ubiquitous obligate intracellular parasite that infects the nucleated cells of warm-blooded animals. From within the parasitophorous vacuole in which they reside, Toxoplasma tachyzoites secrete an arsenal of effector proteins that can reprogram host gene expression to facilitate parasite survival and replication. Gaining a better understanding of how host gene expression is altered upon infection is central for understanding parasite strategies for host invasion and for developing new parasite therapies. Here, we applied ribosome profiling coupled with mRNA measurements to concurrently study gene expression in the parasite and in host human foreskin fibroblasts. By examining the parasite transcriptome and translatome, we identified potential upstream open reading frames that may permit the stress-induced preferential translation of parasite mRNAs. We also determined that tachyzoites reduce host death-associated pathways and increase survival, proliferation, and motility in both quiescent and proliferative host cell models of infection. Additionally, proliferative cells alter their gene expression in ways consistent with massive transcriptional rewiring while quiescent cells were best characterized by re-entry into the cell cycle. We also identified a translational control regimen consistent with mTOR activation in quiescent cells, and to a lesser degree in proliferative cells. This study illustrates the utility of the method for dissection of gene expression programs simultaneously in parasite and host.

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