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

被引:59
作者
Moon, Robert W. [1 ,2 ]
Sharaf, Hazem [3 ]
Hastings, Claire H. [1 ]
Ho, Yung Shwen [3 ]
Nair, Mridul B. [3 ]
Rchiad, Zineb [3 ]
Knuepfer, Ellen [1 ]
Ramaprasad, Abhinay [3 ]
Mohring, Franziska [2 ]
Amir, Amirah [4 ]
Yusuf, Noor A. [1 ,5 ]
Hall, Joanna [6 ]
Almond, Neil [6 ]
Lau, Yee Ling [4 ]
Pain, Arnab [3 ,7 ]
Blackman, Michael J. [1 ,8 ]
Holder, Anthony A. [1 ]
机构
[1] Francis Crick Inst, Mill Hill Lab, London NW7 1AA, England
[2] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Immunol & Infect, London WC1E 7HT, England
[3] King Abdullah Univ Sci & Technol, Biol & Environm Sci & Engn Div, Pathogen Genom Lab, Jeddah 239556900, Saudi Arabia
[4] Univ Malaya, Fac Med, Dept Parasitol, Kuala Lumpur 50603, Malaysia
[5] Inst Med Res, Parasitol Unit, Jalan Pahang, Kuala Lumpur 50588, Malaysia
[6] Hlth Protect Agcy, Natl Inst Biol Stand & Control, Div Retrovirol, Potters Bar EN6 3QG, Herts, England
[7] Hokkaido Univ, Global Inst Collaborat Res & Educ, Res Ctr Zoonosis Control, Sapporo, Hokkaido 0010020, Japan
[8] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Pathogen Mol Biol, London WC1E 7HT, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
invasion; zoonotic malaria; malaria parasite; normocyte-binding protein; Plasmodium knowlesi; COPY NUMBER; VIVAX; FALCIPARUM; ADAPTATION; GENOME; FAMILY; MICRONEMES; CYNOMOLGI; SYSTEM; MONKEY;
D O I
10.1073/pnas.1522469113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:7231 / 7236
页数:6
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