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Normocyte-binding protein required for human erythrocyte invasion by the zoonotic malaria parasite Plasmodium knowlesi
Author(s) -
Robert W. Moon,
Hazem Sharaf,
Claire H. Hastings,
Yung Shwen Ho,
Mridul Nair,
Zineb Rchiad,
Ellen Knuepfer,
Abhinay Ramaprasad,
Franziska Mohring,
Amirah Amir,
Noor A. Yusuf,
Joanna Hall,
Neil Almond,
Yee Ling Lau,
Arnab Pain,
Michael J. Blackman,
Anthony A. Holder
Publication year - 2016
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1522469113
Subject(s) - plasmodium knowlesi , biology , parasite hosting , virology , malaria , plasmodium falciparum , gene , plasmodium (life cycle) , malaria vaccine , genetics , immunology , plasmodium vivax , computer science , world wide web
The dominant cause of malaria in Malaysia is now Plasmodium knowlesi, a zoonotic parasite of cynomolgus macaque monkeys found throughout South East Asia. Comparative genomic analysis of parasites adapted to in vitro growth in either cynomolgus or human RBCs identified a genomic deletion that includes the gene encoding normocyte-binding protein Xa (NBPXa) in parasites growing in cynomolgus RBCs but not in human RBCs. Experimental deletion of the NBPXa gene in parasites adapted to growth in human RBCs (which retain the ability to grow in cynomolgus RBCs) restricted them to cynomolgus RBCs, demonstrating that this gene is selectively required for parasite multiplication and growth in human RBCs. NBPXa-null parasites could bind to human RBCs, but invasion of these cells was severely impaired. Therefore, NBPXa is identified as a key mediator of P. knowlesi human infection and may be a target for vaccine development against this emerging pathogen.

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