Abstract
Antigenic variation of malaria parasites was discovered in P. knowlesi, using a schizont-infected cell agglutination (SICA) assay to detect variant antigens expressed at the surface of infected erythrocytes. Later studies utilizing stable clones, Pk1(A+) and its direct derivative, Pk1(B+)1+, showed that SICA[+] clones express distinct parasite-encoded antigens of approximately 200 kDa. Here we identify a P. knowlesi variant antigen gene and cDNA and demonstrate that it encodes the 205 kDa variant antigen expressed by B+ parasites. This gene belongs to a multigene family, which we term SICAvar. Its ten-exon structure with seven cysteine-rich coding modules is unique compared to P. falciparum var genes. Further, we highlight a 3' genomic alteration that we predict is related to SICAvar gene switching.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Antigenic Variation / genetics*
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Antigens, Surface / genetics*
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Antigens, Surface / immunology
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Clone Cells
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DNA, Complementary / genetics
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Gene Expression Regulation
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Genes, Protozoan*
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Genes, Switch
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Molecular Sequence Data
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Multigene Family
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Plasmodium knowlesi / genetics*
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Plasmodium knowlesi / immunology
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Protein Conformation
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Protozoan Proteins / chemistry
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Protozoan Proteins / genetics*
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Protozoan Proteins / immunology
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Recombinant Fusion Proteins / chemistry
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Recombinant Fusion Proteins / immunology
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Sequence Alignment
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Sequence Homology, Amino Acid
Substances
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Antigens, Surface
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DNA, Complementary
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Protozoan Proteins
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Recombinant Fusion Proteins
Associated data
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GENBANK/AF078128
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GENBANK/AF078129
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GENBANK/AF078130