Malaria parasites target the hepatocyte receptor EphA2 for successful host infection

Alexis Kaushansky(Center for Infectious Disease Research), Alyse N. Douglass(Center for Infectious Disease Research), Nadia Arang(Center for Infectious Disease Research), Vladimir Vigdorovich(Center for Infectious Disease Research), Nicholas Dambrauskas(Center for Infectious Disease Research), Heather S. Kain(Center for Infectious Disease Research), Laura S. Austin(Center for Infectious Disease Research), D. Noah Sather(Center for Infectious Disease Research), Stefan H. I. Kappe(Center for Infectious Disease Research)
Science
November 26, 2015
Cited by 117Open Access
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Abstract

The invasion of a suitable host hepatocyte by mosquito-transmitted Plasmodium sporozoites is an essential early step in successful malaria parasite infection. Yet precisely how sporozoites target their host cell and facilitate productive infection remains largely unknown. We found that the hepatocyte EphA2 receptor was critical for establishing a permissive intracellular replication compartment, the parasitophorous vacuole. Sporozoites productively infected hepatocytes with high EphA2 expression, and the deletion of EphA2 protected mice from liver infection. Lack of host EphA2 phenocopied the lack of the sporozoite proteins P52 and P36. Our data suggest that P36 engages EphA2, which is likely to be a key step in establishing the permissive replication compartment.


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