Abstract
Toxoplasma gondii is an important opportunistic parasite that infects almost all warm-blooded animals, causing congenital neurological and ocular diseases, especially in immunocompromised humans. The available therapeutic drugs are hypersensitive and toxic, and no vaccine is available to block the transmission of this parasite. Safer and more effective drugs are thus urgently needed to treat toxoplasmosis. Protein kinases (PKs) play crucial roles in the proliferation, differentiation, and pathogenesis of T. gondii. T. gondii calcium-dependent protein kinase 1 and cGMP-dependent protein kinase are associated with cell invasion; mitogen-activated protein kinase 1 and cAMP-dependent protein kinase are involved in stress response and conversion from tachyzoite to bradyzoite; casein kinase 1 and cdc2 cyclin-dependent kinase control cell cycle. Rhoptry kinases, the T. gondii-specific PKs, are involved in host manipulation. Because of their difference in structure and function from that of mammalian PKs, T. gondii PKs are promising drug targets. In this review, we describe the functions of T. gondii protein kinases and their inhibitors as potential drugs against T. gondii.
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This work was partially supported by the Chinese National Programs for High Technology Research and Development (No. 2011AA10A215), the Chinese National Nature Science Foundation (No. 31001057 and 31072127), and the Special Fund for Agro-scientific Research in the Public Interest in China (No. 201303042).
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Wei, F., Wang, W. & Liu, Q. Protein kinases of Toxoplasma gondii: functions and drug targets. Parasitol Res 112, 2121–2129 (2013). https://doi.org/10.1007/s00436-013-3451-y
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DOI: https://doi.org/10.1007/s00436-013-3451-y