A Plasmodium falciparum ATP-binding cassette transporter is essential for liver stage entry into schizogony

被引:3
|
作者
Goswami, Debashree [1 ]
Kumar, Sudhir [1 ]
Betz, William [1 ]
Armstrong, Janna M. [1 ]
Haile, Meseret T. [1 ]
Camargo, Nelly [1 ]
Parthiban, Chaitra [2 ,3 ]
Seilie, Annette M. [2 ,3 ]
Murphy, Sean C. [2 ,3 ]
Vaughan, Ashley M. [1 ,4 ]
Kappe, Stefan H. I. [1 ,4 ]
机构
[1] Seattle Childrens Res Inst, Ctr Global Infect Dis Res, 307 Westlake Ave N, Seattle, WA 98101 USA
[2] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
MULTIDRUG-RESISTANCE; MALARIA VACCINES; PARASITES; PROTEIN; POLYMORPHISM; CHLOROQUINE; GENE;
D O I
10.1016/j.isci.2022.104224
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plasmodium sporozoites invade hepatocytes and transform into liver stages within a parasitophorous vacuole (PV). The parasites then grow and replicate their genome to form exoerythrocytic merozoites that infect red blood cells. We report that the human malaria parasite Plasmodium falciparum (Pf) expresses a C-type ATP-binding cassette transporter, Pf ABCC2, which marks the transition from invasive sporozoite to intrahepatocytic early liver stage. Using a humanized mouse infection model, we show that Pf ABCC2 localizes to the parasite plasma membrane in early and mid-liver stage parasites but is not detectable in late liver stages. Pf abcc2(-) sporozoites invade hepatocytes, form a PV, and transform into liver stage trophozoites but cannot transition to exoerythrocytic schizogony and fail to transition to blood stage infection. Thus, Pf ABCC2 is an expression marker for early phases of parasite liver infection and plays an essential role in the successful initiation of liver stage replication.
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页数:22
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