Nature Communications · 2015 · 136 citations · 43 references
Veterinary MedicineInfectious DiseasesPathobiologyGametogenesisInfectious Disease PathologyParasitologyHepatic ParasitismMalariaParasite Life CyclesParasite PhysiologyProtozoan Host-parasite InteractionsProtozoan PathogenesisAllogeneic EngraftmentAutologous EngraftmentHost-parasite SpecificityMalaria Parasite Life CycleMalaria ParasitesMalaria PathologyPlasmodium FalciparumQuiescent Infection
Experimental studies of Plasmodium parasites that infect humans are restricted by their host specificity. Humanized mice offer a means to overcome this and further provide the opportunity to observe the parasites in vivo. Here we improve on previous protocols to achieve efficient double engraftment of TK-NOG mice by human primary hepatocytes and red blood cells. Thus, we obtain the complete hepatic development of P. falciparum, the transition to the erythrocytic stages, their subsequent multiplication, and the appearance of mature gametocytes over an extended period of observation. Furthermore, using sporozoites derived from two P. ovale-infected patients, we show that human hepatocytes engrafted in TK-NOG mice sustain maturation of the liver stages, and the presence of late-developing schizonts indicate the eventual activation of quiescent parasites. Thus, TK-NOG mice are highly suited for in vivo observations on the Plasmodium species of humans.
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Robust expansion of human hepatocytes in Fah−/−/Rag2−/−/Il2rg−/− mice
Hisaya Azuma, Nicole K. Paulk, Aarati R. Ranade et al. · Nature Biotechnology · 2007 · 824 citations · Full text
Mathieu Rougemont, M. van Saanen, Roland Sahli et al. · Journal of Clinical Microbiology · 2004 · 468 citations · Full text
Veterinary Medicine, Infectious Diseases, Molecular Biology +17