The recent sequencing of several apicomplexan genomes has provided the opportunity to characterize novel antigens essential for the parasite life cycle that might lead to the development of new diagnostic and therapeutic markers. Here we have screened the Plasmodium falciparum genome sequence for genes encoding extracellular multidomain putative adhesive proteins. Three of these identified genes, named PfCCp1, PfCCp2, and PfCCp3, have multiple adhesive modules including a common Limulus coagulation factor C domain also found in two additional Plasmodium genes. Orthologues were identified in the Cryptosporidium parvum genome sequence, indicating an evolutionary conserved function. Transcript and protein expression analysis shows sexual stage–specific expression of PfCCp1, PfCCp2, and PfCCp3, and cellular localization studies revealed plasma membrane–associated expression in mature gametocytes. During gametogenesis, PfCCps are released and localize surrounding complexes of newly emerged microgametes and macrogametes. PfCCp expression markedly decreased after formation of zygotes. To begin to address PfCCp function, the PfCCp2 and PfCCp3 gene loci were disrupted by homologous recombination, resulting in parasites capable of forming oocyst sporozoites but blocked in the salivary gland transition. Our results describe members of a conserved apicomplexan protein family expressed in sexual stage Plasmodium parasites that may represent candidates for subunits of a transmission-blocking vaccine.
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7 June 2004
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June 07 2004
A Multidomain Adhesion Protein Family Expressed in Plasmodium falciparum Is Essential for Transmission to the Mosquito
Gabriele Pradel,
Gabriele Pradel
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
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Karen Hayton,
Karen Hayton
2Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases,
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L. Aravind,
L. Aravind
3National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20892
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Lakshminarayan M. Iyer,
Lakshminarayan M. Iyer
3National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20892
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Mitchell S. Abrahamsen,
Mitchell S. Abrahamsen
4Biomedical Genomics Center and Department of Veterinary Pathobiology, University of Minnesota, St. Paul, MN 55108
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Annemarie Bonawitz,
Annemarie Bonawitz
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
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Cesar Mejia,
Cesar Mejia
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
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Thomas J. Templeton
Thomas J. Templeton
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
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Gabriele Pradel
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
Karen Hayton
2Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases,
L. Aravind
3National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20892
Lakshminarayan M. Iyer
3National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20892
Mitchell S. Abrahamsen
4Biomedical Genomics Center and Department of Veterinary Pathobiology, University of Minnesota, St. Paul, MN 55108
Annemarie Bonawitz
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
Cesar Mejia
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
Thomas J. Templeton
1Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10021
Address correspondence to Thomas J. Templeton, Department of Microbiology and Immunology, Weill Medical College of Cornell University, 1300 York Avenue, Box 62, New York, NY 10021. Phone: (212) 746-4467; Fax: (212) 746-4028; email: [email protected]
Abbreviations used in this paper: CS, circumSporozoite; ER, endoplasmic reticulum; IFA, immunofluorescence; LCCL, Limulus coagulation factor C; MBP, maltose-binding protein; SR, scavenger receptor.
The online version of this article contains supplemental material.
Received:
July 28 2003
Accepted:
April 12 2004
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2004
J Exp Med (2004) 199 (11): 1533–1544.
Article history
Received:
July 28 2003
Accepted:
April 12 2004
Citation
Gabriele Pradel, Karen Hayton, L. Aravind, Lakshminarayan M. Iyer, Mitchell S. Abrahamsen, Annemarie Bonawitz, Cesar Mejia, Thomas J. Templeton; A Multidomain Adhesion Protein Family Expressed in Plasmodium falciparum Is Essential for Transmission to the Mosquito . J Exp Med 7 June 2004; 199 (11): 1533–1544. doi: https://doi.org/10.1084/jem.20031274
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