The Toxoplasma gondii Rhoptry Kinome Is Essential for Chronic Infection

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The Toxoplasma gondii Rhoptry Kinome Is Essential for Chronic Infection

UNLABELLED Ingestion of the obligate intracellular protozoan parasite Toxoplasma gondii causes an acute infection that leads to chronic infection of the host. To facilitate the acute phase of the infection, T. gondii manipulates the host response by secreting rhoptry organelle proteins (ROPs) into host cells during its invasion. A few key ROP proteins with signatures of kinases or pseudokinases...

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Functional Analysis of the Rhoptry Kinome during Chronic Toxoplasma gondii Infection

Toxoplasma gondii is one of the most common parasitic infections of humans worldwide. Once exposed, humans remain infected with T. gondii for life, and there are no therapeutics capable of eliminating a chronic infection. In the search for novel drug targets, T. gondii is known to contain several unique secretory organelles, one of which is called the rhoptries. Rhoptry organelles contain and s...

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Functional Characterization of Rhoptry Kinome in the Virulent Toxoplasma gondii RH Strain

Toxoplasma gondii is an obligatory intracellular apicomplexan protozoan which can infect any warm-blooded animal and causes severe diseases in immunocompromised individuals or infants infected in utero. The survival and success of this parasite require that it colonizes the host cell, avoids host immune defenses, replicates within an appropriate niche, and exits the infected host cell to spread...

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Cactin is essential for G1 progression in Toxoplasma gondii.

Toxoplasma gondii is an obligate intracellular protozoan parasite whose rapid lytic replication cycles define its pathogenicity. We identified a temperature-sensitive growth mutant, FV-P6, which irreversibly arrests before the middle of the G1 stage of the tachyzoite cell cycle. This arrest is caused by a point mutation in a gene conserved across eukaryotes, Cactin, whose product localizes to t...

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ژورنال

عنوان ژورنال: mBio

سال: 2016

ISSN: 2161-2129,2150-7511

DOI: 10.1128/mbio.00193-16