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    Normocyte-binding protein required for human erythrocyte invasion by the zoonotic malaria parasitePlasmodium knowlesi

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    Type
    Article
    Authors
    Moon, Robert W. cc
    Sharaf, Hazem
    Hastings, Claire H.
    Shwen, Ho cc
    Nair, Mridul
    Rchiad, ‍Zineb cc
    Knuepfer, Ellen
    Ramaprasad, Abhinay cc
    Mohring, Franziska
    Amir, Amirah
    Yusuf, Noor A.
    Hall, Joanna
    Almond, Neil
    Lau, Yee Ling
    Pain, Arnab cc
    Blackman, Michael J. cc
    Holder, Anthony A. cc
    KAUST Department
    Biological and Environmental Sciences and Engineering (BESE) Division
    Bioscience Program
    Computational Bioscience Research Center (CBRC)
    Pathogen Genomics Laboratory
    Date
    2016-06-14
    Online Publication Date
    2016-06-14
    Print Publication Date
    2016-06-28
    Permanent link to this record
    http://hdl.handle.net/10754/621436
    
    Metadata
    Show full item record
    Abstract
    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.
    Citation
    Moon RW, Sharaf H, Hastings CH, Ho YS, Nair MB, et al. (2016) Normocyte-binding protein required for human erythrocyte invasion by the zoonotic malaria parasitePlasmodium knowlesi. Proc Natl Acad Sci USA 113: 7231–7236. Available: http://dx.doi.org/10.1073/pnas.1522469113.
    Sponsors
    This work was supported by the Francis Crick Institute, which receives its core funding from Cancer Research UK, the UK Medical Research Council (MRC), and the Wellcome Trust. The work was further supported by the UK MRC (Grants U117532063 and U117532067), the European Community's Seventh Framework Programme under Grant Agreement 242095 (EviMalar), an MRC Career Development Award (to R.W.M.) jointly funded by the UK MRC and Department for International Development, and the faculty baseline fund (BRF) from the King Abdullah University of Science and Technology (to A.P.). A.A. and Y.L.L. were funded by a UM High Impact Research (HIR) Grant UM-MOHE (UM.C/HIR/MOHE/MED/16) from the Ministry of Higher Education Malaysia.
    Publisher
    Proceedings of the National Academy of Sciences
    Journal
    Proceedings of the National Academy of Sciences
    DOI
    10.1073/pnas.1522469113
    PubMed ID
    27303038
    ae974a485f413a2113503eed53cd6c53
    10.1073/pnas.1522469113
    Scopus Count
    Collections
    Articles; Biological and Environmental Science and Engineering (BESE) Division; Bioscience Program; Computational Bioscience Research Center (CBRC)

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