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© Liliana Mancio, Institut Pasteur
Primary human hepatocytes co-cultured with parenchymal cells at 6 days post-seeding. The expression of human CD81 is depicted in pink
Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Nature communications - 15 Jul 2022

Luiza-Batista C, Thiberge S, Serra-Hassoun M, Nardella F, Claës A, Nicolete VC, Commère PH, Mancio-Silva L, Ferreira MU, Scherf A, Garcia S,

Link to Pubmed [PMID] – 35840625

Link to DOI – 10.1038/s41467-022-31864-6

Nat Commun 2022 Jul; 13(1): 4123

Plasmodium vivax is the most widespread human malaria parasite. Due to the presence of extravascular reservoirs and relapsing infections from dormant liver stages, P. vivax is particularly difficult to control and eliminate. Experimental research is hampered by the inability to maintain P. vivax cultures in vitro, due to its tropism for immature red blood cells (RBCs). Here, we describe a new humanized mice model that can support efficient human erythropoiesis and maintain long-lasting multiplication of inoculated cryopreserved P. vivax parasites and their sexual differentiation, including in bone marrow. Mature gametocytes were transmitted to Anopheles mosquitoes, which led to the formation of salivary gland sporozoites. Importantly, blood-stage P. vivax parasites were maintained after the secondary transfer of fresh or frozen infected bone marrow cells to naïve chimeras. This model provides a unique tool for investigating, in vivo, the biology of intraerythrocytic P. vivax.