Moon Robert W, Sharaf Hazem, Hastings Claire H, Ho Yung Shwen, Nair Mridul B, Rchiad Zineb, Knuepfer Ellen, Ramaprasad Abhinay, Mohring Franziska, Amir Amirah, Yusuf Noor A, Hall Joanna, Almond Neil, Lau Yee Ling, Pain Arnab, Blackman Michael J, Holder Anthony A
Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, United Kingdom; Department of Immunology and Infection, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, United Kingdom;
Pathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Jeddah 23955-6900, Kingdom of Saudi Arabia;
Proc Natl Acad Sci U S A. 2016 Jun 28;113(26):7231-6. doi: 10.1073/pnas.1522469113. Epub 2016 Jun 14.
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.
马来西亚疟疾的主要病因目前是诺氏疟原虫,这是一种在东南亚各地猕猴体内发现的人畜共患寄生虫。对适应于在食蟹猴或人类红细胞中进行体外生长的寄生虫进行的比较基因组分析,确定了一个基因组缺失,该缺失包括编码正常红细胞结合蛋白Xa(NBPXa)的基因,该基因存在于在食蟹猴红细胞中生长的寄生虫中,但在人类红细胞中生长的寄生虫中不存在。在适应于在人类红细胞中生长的寄生虫(保留在食蟹猴红细胞中生长的能力)中实验性删除NBPXa基因,将它们限制在食蟹猴红细胞中生长,表明该基因是寄生虫在人类红细胞中增殖和生长所选择性必需的。无NBPXa的寄生虫可以与人红细胞结合,但这些细胞的侵入严重受损。因此,NBPXa被确定为诺氏疟原虫人类感染的关键介质,可能是针对这种新出现病原体的疫苗开发靶点。