| Literature DB >> 27303038 |
Robert W Moon1, Hazem Sharaf2, Claire H Hastings3, Yung Shwen Ho2, Mridul B Nair2, Zineb Rchiad2, Ellen Knuepfer3, Abhinay Ramaprasad2, Franziska Mohring4, Amirah Amir5, Noor A Yusuf6, Joanna Hall7, Neil Almond7, Yee Ling Lau5, Arnab Pain8, Michael J Blackman9, Anthony A Holder10.
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.Entities:
Keywords: Plasmodium knowlesi; invasion; malaria parasite; normocyte-binding protein; zoonotic malaria
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Year: 2016 PMID: 27303038 PMCID: PMC4933575 DOI: 10.1073/pnas.1522469113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205