Conditional expression of apical membrane antigen 1 in Plasmodium falciparum shows it is required for erythrocyte invasion by merozoites

被引:80
|
作者
Yap, Alan [1 ]
Azevedo, Mauro F. [2 ]
Gilson, Paul R. [2 ]
Weiss, Greta E. [2 ]
O'Neill, Matthew T. [1 ]
Wilson, Danny W. [1 ]
Crabb, Brendan S. [2 ]
Cowman, Alan F. [1 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3052, Australia
[2] Macfarlane Burnet Inst Med Res & Publ Hlth, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
HOST-CELL INVASION; RED-BLOOD-CELLS; APICOMPLEXAN PARASITES; MALARIA PARASITES; CRE RECOMBINASE; RHOPTRY; AMA1; PROTEINS; VACCINE; RON2;
D O I
10.1111/cmi.12287
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Malaria is caused by obligate intracellular parasites, of which Plasmodium falciparum is the most lethal species. In humans, P.falciparum merozoites (invasive forms of the parasite) employ a host of parasite proteins to rapidly invade erythrocytes. One of these is the P.falciparum apical membrane antigen 1 (PfAMA1) which forms a complex with rhoptry neck proteins at the tight junction. Here, we have placed the Pfama1 gene under conditional control using dimerizable Cre recombinase (DiCre) in P.falciparum. DiCre-mediated excision of the loxP-flanked Pfama1 gene results in approximately 80% decreased expression of the protein within one intraerythrocytic growth cycle. This reduces growth by 40%, due to decreased invasion efficiency characterized by a post-invasion defect in sealing of the parasitophorous vacuole. These results show that PfAMA1 is an essential protein for merozoite invasion in P.falciparum and either directly or indirectly plays a role in resealing of the red blood cell at the posterior end of the invasion event.
引用
收藏
页码:642 / 656
页数:15
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