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An analysis of the development of resistance to metachloridine in clones of Plasmodium gallinaceum

Published online by Cambridge University Press:  06 April 2009

Ann Bishop
Affiliation:
Member of the Staff of the Medical Research Council. Molteno Institute, University of Cambridge

Extract

1. The development of resistance to metachloridine (3-metanilamido-5-chloropyrimidine) was studied in two clones of Plasmodium gallinaceum derived from single erythrocytic parasites and maintained by serial inoculation in young chicks. Resistance developed with equal facility and similarly in the two clones.

2. In thirteen strains of these clones an enhancement of resistance was obtained after three to five courses of treatment, each of seven doses of metachloridine over a period of 3½ days.

3. The effect of the size of the inoculum (2·5 × 107–109 parasites), and of the dose of drug upon the rate of development of resistance was studied. Although the number of courses of treatment required to produce an enhancement of resistance was not always related to the size of the inoculum, with the largest inoculum an enhancement of resistance was observed after the minimum number of courses of treatment (three), whereas with the smallest inoculum no enhancement of resistance was obtained. The rate of the development of resistance did not appear to be related to the size of the dose of drug.

4. In some strains the increase in resistance was sudden, whereas in others it was more gradual. Resistance was retained when parasites of a newly resistant strain were transmitted through Aëdes aegypti or maintained for 43 days in the absence of the drug.

5. A comparison of the development of resistance in populations of normal parasites, and of populations composed of mixtures of known numbers of resistant and normal parasites, indicated that the pattern of the development of resistance in normal populations could be explained by the selections of mutations of a frequency of less than 1 in 5 × 107, or probably less than 1 in 109 parasites.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1958

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References

Bishop, A. & McConnachie, E. W. (1950). Sulphadiazine-resistance in Plasmodium gallinaceum and its relation to other antimalarial compounds. Parasitology, 40, 163.CrossRefGoogle ScholarPubMed
Bishop, A. & McConnachie, E. W. (1952 a). Failure to produce resistance to chloroquine in Plasmodium gallinaceum in chicks. Parasitology, 42, 52.Google Scholar
Bishop, A. & McConnachie, E. W. (1952 b). Pamaquin resistance in a strain of Plasmodium gallinaceum and its relationship to other antimalarial drugs. Parasitology, 42, 57.CrossRefGoogle Scholar
Bishop, A. & McConnachie, E. W. (1953). The development of resistance to metachloride in Plasmodium gallinaceum in chicks. Parasitology, 42, 277.CrossRefGoogle Scholar
Coulston, F. & Manwell, R. D. (1941). Single-parasite infections and exoerythrocytic schizogony in Plasmodium circumflexum. Amer. J. Hyg. 34, 119.Google Scholar
Curd, F. H. S., Davey, D. G. & Rose, F. L. (1945). Studies on synthetic antimalarial drugs. I. Biological methods. Ann. Trop. Med. Parasit. 39, 139.Google Scholar
Dean, A. C. R. & Hinshelwood, Sir Cyril (1957). Aspects of the problem of drug resistance in bacteria. Ciba Foundation symposium on Drug resistance in Microorganisms. London: J. & A. Churchill Ltd.Google Scholar
Demidowa, L. W. (1934). Ueber die geringste zur Erzeugung der experimentellen Malaria nötige Plasmodium gallinaceum. G. Batt. Immun. 13, 872.Google Scholar
Downs, W. G. (1947). Infections of chicks with single parasites of Plasmodium gallinaceum Brumpt. Amer. J. Hyg. 46, 41.Google ScholarPubMed
Giovannola, A. (1938). Il Plasmodium gallinaceum Brumpt 1935, i così detti corpi toxoplasmasimili ed alcune inclusioni di probabile natura parassitaria nei globuli bianchi del Gallus gallus. Riv. Parassit. 2, 129.Google Scholar
Lumsden, W. H. R. & Bertram, D. S. (1940). Observations on the biology of Plasmodium gallinaceum Brumpt, 1935, in the domestic fowl, with special reference to the production of gametocytes and their development in Aëdes aegypti (L). Ann. Trop. Med. Parasit. 34, 135.Google Scholar
Ray, A. P., Sharma, G. K. & Misra, B. G. (1956). Screening of antimalarials against P. gallinaceum in chicks. VI. Evidence of two-fold acquired resistance to chloroquine diphosphate in a strain of P. gallinaceum in chicks. Ind. J. Malar. 10, 299.Google Scholar
Sonneborn, T. M. (1947). Recent advances in the genetics of Paramecium and Euplotes. Advanc. Genet. 1, 263.CrossRefGoogle ScholarPubMed
Taliaferro, W. H. & Taliaferro, L. G. (1950). Reproduction-inhibiting and parasiticidal effects of Plasmodium gallinaceum and Plasmodium lophurae during initial infection and homologous superinfection in chickens. J. Infect. Dis. 86, 275.Google Scholar
Williamson, J. & Lourie, E. M. (1947). Acquired paludrine-resistance in Plasmodium gallinaceum. I. Development of resistance to paludrine and failure to develop resistance to certain other antimalarials. Ann. trop. Med. Parasit. 41, 278.Google Scholar
Young, M. D. (1957). Resistance of Plasmodium malariae to pyrimethamince (daraprim). Amer. J. Trop. Med. 6, 621.Google Scholar