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Plasmodium sporozoites, the mosquito-transmitted forms of the malaria parasite, first infect the liver for an initial round of replication before the emergence of pathogenic blood stages. Sporozoites represent attractive targets for antimalarial preventive strategies, yet the mechanisms of parasite entry into hepatocytes remain poorly understood. Here we show that the two main species causing malaria in humans, Plasmodium falciparum and Plasmodium vivax, rely on two distinct host cell surface proteins, CD81 and the Scavenger Receptor BI (SR-BI), respectively, to infect hepatocytes. By contrast, CD81 and SR-BI fulfil redundant functions during infection by the rodent parasite P. berghei. Genetic analysis of sporozoite factors reveals the 6-cysteine domain protein P36 as a major parasite determinant of host cell receptor usage. Our data provide molecular insights into the invasion pathways used by different malaria parasites to infect hepatocytes, and establish a functional link between a sporozoite putative ligand and host cell receptors.

Original publication

DOI

10.7554/eLife.25903

Type

Journal article

Journal

Elife

Publication Date

16/05/2017

Volume

6

Keywords

P. berghei, P. falciparum, P. vivax, P. yoelii , hepatocyte, human, infectious disease, malaria, microbiology, mouse, sporozoite, Animals, Cell Line, Endocytosis, Hepatocytes, Host-Pathogen Interactions, Humans, Membrane Proteins, Plasmodium berghei, Plasmodium falciparum, Plasmodium vivax, Protozoan Proteins, Rodentia, Scavenger Receptors, Class B, Sporozoites, Tetraspanin 28