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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.
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页码:642 / 656
页数:15
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