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Normocyte-binding protein required for human erythrocyte invasion by the zoonotic malaria parasite Plasmodium knowlesi.
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.
Afiliación
  • Moon RW; 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; Rob.Moon@lshtm.ac.uk Tony.Holder@crick.ac.uk.
  • Sharaf H; 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;
  • Hastings CH; Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, United Kingdom;
  • Ho YS; 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;
  • Nair MB; 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;
  • Rchiad Z; 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;
  • Knuepfer E; Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, United Kingdom;
  • Ramaprasad A; 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;
  • Mohring F; Department of Immunology and Infection, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, United Kingdom;
  • Amir A; Department of Parasitology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia;
  • Yusuf NA; Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, United Kingdom; Parasitology Unit, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia;
  • Hall J; Division of Retrovirology, National Institute for Biological Standards and Control, Health Protection Agency, Hertfordshire EN6 3QG, United Kingdom;
  • Almond N; Division of Retrovirology, National Institute for Biological Standards and Control, Health Protection Agency, Hertfordshire EN6 3QG, United Kingdom;
  • Lau YL; Department of Parasitology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia;
  • Pain A; 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; Research Center for Zoonosis Control, Global Institution for Collaborative Research and Education, Hok
  • Blackman MJ; Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, United Kingdom; Department of Pathogen Molecular Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, United Kingdom.
  • Holder AA; Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, United Kingdom; Rob.Moon@lshtm.ac.uk Tony.Holder@crick.ac.uk.
Proc Natl Acad Sci U S A ; 113(26): 7231-6, 2016 06 28.
Article en En | MEDLINE | ID: mdl-27303038
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Portadoras / Proteínas Protozoarias / Plasmodium knowlesi / Eritrocitos Límite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Portadoras / Proteínas Protozoarias / Plasmodium knowlesi / Eritrocitos Límite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article