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Short-term culture of Plasmodium knowlesi

Published online by Cambridge University Press:  06 April 2009

G. A. Butcher
Affiliation:
Department of Chemical Pathology, Guy's Hospital Medical School, London, S.E. 1
S. Cohen
Affiliation:
Department of Chemical Pathology, Guy's Hospital Medical School, London, S.E. 1

Extract

The culture method developed by Geiman and co-workers has been modified to give average multiplication rates for Plasmodium knowlesi of at least six-fold in 24 h.

Individual modifications have been assessed on the basis of parasite multiplication and [3H]leucine incorporation into parasite protein. The second cycle of in vitro development which is particularly influenced by the conditions of culture was improved by: (i) culture of washed parasitized red cells in a medium containing dialysed homologous serum screened for its ability to support parasite growth; (ii) addition of ATP, Co-enzyme A (or pantothenate) and glutamine.

We thank Mr E. D. Dennis and Miss Susan Wanstall for technical assistance. This work was supported by grants from the Medical Research Council and the World Health Organization.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1971

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References

REFERENCES

Anfinson, C. B., Geiman, Q. M., Mckee, R. W., Ormsbee, R. A. & Ball, E. G. (1946). Studies on malarial parasites; VIII. Factors affecting the growth of Plasmodium knowlesi in vitro. Journal of Experimental Medicine 84, 607–21.Google Scholar
Ball, E. G., Anfinsen, C. B., Geiman, Q. M., Mckee, R. W. & Ormsbee, R. A. (1945). In vitro growth and multiplication of malaria parasite, Plasmodium knowlesi. Science 101; 542–4.CrossRefGoogle ScholarPubMed
Bass, C. C. & Johns, F. M. (1912). The cultivation of malarial plasmodia (Plasmodium vivax and Plasmodium falciparum) in vitro. Journal of Experimental Medicine 16, 567–79.CrossRefGoogle ScholarPubMed
Bennet, T. P. & Trager, W. (1967). Pantothenic acid metabolism during avian malaria infection; pantothenate kinase activity in duck erythrocytes and in Plasmodium lophurae. Journal of Protozoology 14, 214–6.CrossRefGoogle Scholar
Brewer, G. J. & Powell, R. D. (1965). A study of the relationship between the content of adenosine triphosphate in human red cells and the course of falciparum malaria: A new system that may confer protection against malaria. Proceedings of the National Academy of Sciences of the United States of America 54, 741–5.CrossRefGoogle ScholarPubMed
Buhler, D. R. (1962). A sinple scintillation counting technique for assaying C14O2 in a Warburg flask. Analytical Biochemistry 4, 413.CrossRefGoogle Scholar
Cohen, S., Butcher, G. A. & Crandall, R. B. (1969). Action of Malarial Antibody in vitro. Nature 223, 368.CrossRefGoogle ScholarPubMed
Cohen, S. & Butcher, G. A. (1970). Properties of protective malarial antibody. Nature 225, 732.CrossRefGoogle ScholarPubMed
Eaton, J. W. & Brewer, G. J. (1969). Red cell ATP and malaria infection. Nature 222, 389.CrossRefGoogle ScholarPubMed
Garnham, P. C. C. (1966). In Malaria Parasites. Oxford: Blackwell.Google ScholarPubMed
Geiman, Q. M., Anfinsen, C. B., Mckee, R. W., Ormsbee, R. A. & Ball, E. G. (1946). Studies on malarial parasites; methods and techniques for cultivation. Journal of Experimental Medicine 84, 583606.CrossRefGoogle ScholarPubMed
Geiman, Q. M., Siddiqui, W. A. & Schnell, J. W. (1966). In vitro studies on erythrocytic stages of plasmodia; medium improvements and results with seven species of malarial parasites. Military Medicine 131 (Supplement), 1015–25.CrossRefGoogle ScholarPubMed
Mckee, R. W., Ormsbee, R. A., Anfinsen, C. B., Geiman, Q. M. & Ball, E. G. (1946). Studies on malarial parasites; chemistry and metabolism of normal and parasitised (P. knowlesi) monkey blood. Journal of Experimental Medicine 84, 569–82.CrossRefGoogle Scholar
Riley, M. V. & Maegraith, B. G. (1961). A factor in the serum of malaria-infected animals capable of inhibiting the in vitro oxidative metabolism of normal liver mitochondria. Annals of Tropical Medicine and Parasitology 55, 489–97.CrossRefGoogle ScholarPubMed
Sherman, I. W., Ruble, J. A. & Tanigoshi, L. (1969). Incorporation of 14C-amino acids by malaria (Plasmodium lophurae) I. Role of ions and amino acids in the medium. Military Medicine 134, 954–61.CrossRefGoogle ScholarPubMed
Siddiqui, W. A., Schnell, J. V. & Geiman, Q. M. (1967). Stearic acid as plasma replacement for intracellular in vitro cultures of Plasmodium knowlesi. Science 156, 1623–5.CrossRefGoogle ScholarPubMed
Terasaki, P. I., Esail, M. L., Cannon, J. A. & Longmire, W. P. (1961). Destruction of Lymphocytes in vitro by normal serum from common laboratory animals. Journal of Immunology 87, 383–95.CrossRefGoogle ScholarPubMed
Trager, W. (1950). Studies on extracellular cultivation of intracellular parasite (avian malaria); development of organisms in erythrocytic extracts, and favouring effect of adenosine triphosphate. Journal of Experimental Medicine 92, 349–66.CrossRefGoogle Scholar
Trager, W. (1965). Cultivation of intracellular protozoa. The role of the host cell with special reference to Coenzyme A and the antimalarial action of an anti pantothenate. 2nd International Conference on Protozoology, London 97–8 (Abstract).Google Scholar
Trigg, P. I. (1967). In vitro growth of Plasmodium knowlesi and P. falciparum. Nature 213, 1019.CrossRefGoogle Scholar
Trigg, P. I. (1968). A new continuous perfusion technique for the cultivation of malaria parasites in vitro. Transactions of the Royal Society of Tropical Medicine & Hygiene 62, 371–8.CrossRefGoogle Scholar
Trigg, P. I. (1969). Some factors affecting the cultivation in vitro of the erythrocytic stages of Plasmodium knowlesi. Parasitology 59, 915–24.CrossRefGoogle ScholarPubMed