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. 1980 Apr 1;151(4):790–798. doi: 10.1084/jem.151.4.790

Determinants on surface proteins of Plasmodium knowlesi merozoites common to Plasmodium falciparum schizonts

PMCID: PMC2185834  PMID: 6154761

Abstract

In this report and (R. Schmidt-Ullrich, L. H. Miller, and D. F. H. Wallach. Manuscript in preparation.), we have demonstrated that malaria proteins on the surface of merozoites and infected erythrocytes cross- react between at least two primate malarias, Plasmodium knowlesi and P. falciparum. Sera from five Gambian adults who were highly immune to P. falciparum were used as a reagent to study the cross-reactivity between P. falciparum schizonts and surface proteins on P. knowlesi merozoites. Although the sera bound to the surface of viable, intact P. knowlesi merozoites, the sera did not block invasion of rhesus erythrocytes. 125I-lactoperoxidase-labeled surface proteins on merozoites formed complexes with the antibody. All major protein bands seen in the electrophoresis of the original Triton extract were bound by the immune sera. Because Gambians have never been exposed to P. knowlesi malaria, the antibodies that reacted with P. knowlesi merozoites must be directed against antigens of another parasite such as P. falciparum. We tested this hypothesis by competition for antibody in a Gambian serum between Triton-extracted antigens from P. falciparum schizont-infected erythrocytes and from surface-labeled P. knowlesi merozoites. P. falciparum inhibited the reaction, thus indicating cross-reaction between antigens in P. falciparum schizonts and P. knowlesi merozoites.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bensadoun A., Weinstein D. Assay of proteins in the presence of interfering materials. Anal Biochem. 1976 Jan;70(1):241–250. doi: 10.1016/s0003-2697(76)80064-4. [DOI] [PubMed] [Google Scholar]
  2. Butcher G. A., Mitchell G. H., Cohen S. Antibody mediated mechanisms of immunity to malaria induced by vaccination with Plasmodium knowlesi merozoites. Immunology. 1978 Jan;34(1):77–86. [PMC free article] [PubMed] [Google Scholar]
  3. Collins W. E., Jeffery G. M., Guinn E., Skinner J. C. Fluorescent antibody studies in human malaria. IV. Cross-reactions between human and simian malaria. Am J Trop Med Hyg. 1966 Jan;15(1):11–15. doi: 10.4269/ajtmh.1966.15.11. [DOI] [PubMed] [Google Scholar]
  4. Deans J. A., Dennis E. D., Cohen S. Antigenic analysis of sequential erythrocytic stages of Plasmodium knowlesi. Parasitology. 1978 Dec;77(3):333–344. doi: 10.1017/s0031182000050290. [DOI] [PubMed] [Google Scholar]
  5. Eaton M. D., Coggeshall L. T. COMPLEMENT FIXATION IN HUMAN MALARIA WITH AN ANTIGEN PREPARED FROM THE MONKEY PARASITE PLASMODIUM KNOWLESI. J Exp Med. 1939 Feb 28;69(3):379–398. doi: 10.1084/jem.69.3.379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Haynes J. D., Diggs C. L., Hines F. A., Desjardins R. E. Culture of human malaria parasites Plasmodium falciparum. Nature. 1976 Oct 28;263(5580):767–769. doi: 10.1038/263767a0. [DOI] [PubMed] [Google Scholar]
  7. Jeffery G. M. Epidemiological significance of repeated infections with homologous and heterologous strains and species of Plasmodium. Bull World Health Organ. 1966;35(6):873–882. [PMC free article] [PubMed] [Google Scholar]
  8. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  9. Lambros C., Vanderberg J. P. Synchronization of Plasmodium falciparum erythrocytic stages in culture. J Parasitol. 1979 Jun;65(3):418–420. [PubMed] [Google Scholar]
  10. Morrison M. The determination of the exposed proteins on membranes by the use of lactoperoxidase. Methods Enzymol. 1974;32:103–109. doi: 10.1016/0076-6879(74)32013-7. [DOI] [PubMed] [Google Scholar]
  11. Schmidt-Ullrich R., Wallach D. F. Plasmodium knowlesi-induced antigens in membranes of parasitized rhesus monkey erythrocytes. Proc Natl Acad Sci U S A. 1978 Oct;75(10):4949–4953. doi: 10.1073/pnas.75.10.4949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Schmidt L. H. Plasmodium falciparum and Plasmodium vivax infections in the owl monkey (Aotus trivirgatus). I. The courses of untreated infections. Am J Trop Med Hyg. 1978 Jul;27(4):671–702. doi: 10.4269/ajtmh.1978.27.671. [DOI] [PubMed] [Google Scholar]
  13. Trager W., Jensen J. B. Human malaria parasites in continuous culture. Science. 1976 Aug 20;193(4254):673–675. doi: 10.1126/science.781840. [DOI] [PubMed] [Google Scholar]
  14. Voller A., Rossan R. N. Immunological studies on simian malaria parasites. IV. Heterologous superinfection of monkeys with chronic Plasmodium knowlesi infections. Trans R Soc Trop Med Hyg. 1969;63(6):837–845. doi: 10.1016/0035-9203(69)90129-1. [DOI] [PubMed] [Google Scholar]

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