Hostname: page-component-77c89778f8-gq7q9 Total loading time: 0 Render date: 2024-07-22T19:22:37.907Z Has data issue: false hasContentIssue false

On Trypanosoma brucei, T. rhodesiense and T. gambiense and their Ability to Infect Man

Published online by Cambridge University Press:  06 April 2009

H. Lyndhurst Duke
Affiliation:
From the Human Trypanosomiasis Research Institute Entebbe, Uganda

Extract

1. A strain of T. rhodesiense, isolated from man and readily transmissible by tsetse, was passed by direct inoculation through a series of fourteen guineapigs over a period of 18 months. At the end of that time it had lost its transmissibility by Glossina palpalis, and it also failed to infect a volunteer.

2. Another line of the same strain, after 98 days in a bushbuck, 30 days in a fowl and 294 days in oxen, proved still readily transmissible by G. palpalis and also readily infective to man.

3. A second strain underwent seven consecutive cyclical passages through tsetse, then two passages by the syringe, and finally another cyclical passage, all save one in monkeys. When tested on man at the tenth and eleventh passages it was found to be non-infective.

4. A strain of T. gambiense, isolated in November 1920 from a patient from Fernando Po, was found in February 1934 to be readily infective to man. The strain was entirely non-transmissible by and almost completely non-infective to G. palpalis.

5. Three strains of T. brucei, one from the west, one from the north and one from the south of Uganda Protectorate, were found to be incapable of infecting normal healthy man. All the tests were carried out with cyclically infected tsetse.

6. A freshly isolated strain of T. gambiense from a Uganda native was transmitted to man by cyclically infected laboratory-bred G. palpalis.

7. A strain of T. rhodesiense, shortly after its recovery from a native of Tanganyika Territory, underwent three successive cyclical passages by laboratory-bred G. palpalis from monkey to monkey; at each passage the strain was tested on man and found to be readily infective.

8. A strain from Nigeria showing points of resemblance to both T. gambiense and T. rhodesiense was found to be pathogenic to man, on subcutaneous inoculation of infected blood, three years after its first isolation.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1935

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Adams, A. R. D. (1933). A record of an investigation into the action of sera on the trypanosomes pathogenic to man. Ann. Trop. Med. and Parasitol. 27, 309.CrossRefGoogle Scholar
Corson, J. F. (1932). Experiments on the transmission of Trypanosomes brucei and Trypanosomes rhodesiense to man. Ann. Trop. Med. and Parasitol. 26, 109.CrossRefGoogle Scholar
Corson, J. F. (1933). A further note on the action of normal human serum on Trypanosomes rhodesiense in relation to cyclical passage through tsetse flies. J. Trop. Med. and Hyg. 36, 378.Google Scholar
Duke, H. L. (1912). Antelope as a reservoir of Trypanosomes gambiense. Proc. Roy. Soc. B, 85, 299.Google Scholar
Duke, H. L. (1919). Tsetse flies and Trypanosomiasis. Parasitology, 11, 415.CrossRefGoogle Scholar
Duke, H. L. (1921). On the zoological status of the polymorphic trypanosomes of Africa and their relation to man. Parasitology 13, 352.CrossRefGoogle Scholar
Duke, H. L. (1923). Further inquiries into the zoological status of the polymorphic mammalian trypanosomes of Africa, and the means by which they are spread in nature. Parasitology 15, 258.CrossRefGoogle Scholar
Duke, H. L. (1923 a). An inquiry into an outbreak of human trypanosomiasis in a “Glossina morsitans” belt to the East of Mwanza, Tanganyika Territory. Proc. Roy. Soc. B, 94, 250.Google Scholar
Duke, H. L. (1928). Final Report of the League of Nations International Commission on Human Trypanosomiasis, Geneva, C.H. 629, 1928.Google Scholar
Duke, H. L. (1932). The polymorphic trypanosomes of Damba Island, Victoria Nyanza. I. Their ability to infect man. Ann. Trop. Med. and Parasitol. 26, 191.CrossRefGoogle Scholar
Duke, H. L. (1933). The trypanosomes of man; their resistance to arsenical drugs. Lancet, Sept. 2, p. 333.Google Scholar
Duke, H. L. (1934). Studies on the factors that may influence the transmission of the polymorphic trypanosomes by tsetse. VIII. The effect of cyclical passage through Glossina. Ann. Trop. Med. and Parasitol. 28, No. I, pp. 79–91. [See also note dated May 18, 1934, relating to VIII. Ibid. 29, No. 2, p. 244.]CrossRefGoogle Scholar
Duke, H. L. (1934 a). On the transmissibility by Glossinaof Trypanosomes brucei, T. rhodesiense and T. gambiense, with special reference to old laboratory strains. Parasitology, 26, p. 153–62.CrossRefGoogle Scholar
Duke, H. L. (1934 b). On the employment of volunteers in trypanosomiasis research; and on the element of control in experiments with trypanosomes and Glossinae. Parasitology 26, 315.CrossRefGoogle Scholar
Duke, H. L. (1934 c). On the protective action of “Bayer 205” against the trypanosomes of man. Lancet, June 23rd, p. 1336.CrossRefGoogle Scholar
Duke, H. L. (1935). Further studies of the behaviour of T. rhodesiense, recently isolated from man, in antelope and other African game animals. Parasitology, 27, 68.CrossRefGoogle Scholar
Fairbairn, H. (1933). The action of human ser. in vitro on sixty-four recently isolated strains of T. rhodesiense. Ann. Trop. Med. and Parasitol. 27, 788.CrossRefGoogle Scholar
James, S. P. (1931). Some general results of a study of induced malaria in England. Trans. Roy. Soc. Trop. Med. and Hyg. 24, 477.CrossRefGoogle Scholar
James, S. P., Nicol, W. D. and Shute, P. G. (1927). Experiments on the treatment of malaria in England. Trans. F.E.A.T.M. Seventh Congress, 2, 788.Google Scholar
Kleine, F. K. (1923). Zur Epidemiologie der Schlafkrankheit. Dtsch. med. Wschr. Apr. 20, 505.CrossRefGoogle Scholar
Lester, H. M. O. (1933). The influence of cyclical transmission by Glossina tachinoides on a strain of Trypanosomes brucei, made resistant to human serum. Ann. Trop. Med. and Parasitol. 26, 525.CrossRefGoogle Scholar
Schilling, C. and Schreck, H. (1930). Bleiben erworbene biologische Eigenschaften pathogener Protozoen bei der Passage durch die natürlichen Ueberträger erhalten? Dtsch. med. Wschr. No. 28.CrossRefGoogle Scholar
Swellengrebel, N. H., De Buck, M. A. and Swellengrebel De Graaf, M. I. M. H. (1929). A malarial infection in Holland acquired during the autumn does not become manifest till the next summer. Geneva, Malaria Commission, C.H. (Malaria), p. 136.Google Scholar
Taute, M. (1913). Untersuchungen über die Bedeutung des Grosswildes und der Haustiere für die Verbreitung der Schlafkrankheit. Arbeit. a. d. Kaiserl. Gesundheitsamt, 45, 102.Google Scholar
Taute, M. and Huber, F. (1919). Die Unterscheidung des Trypanosomes rhodesiense vom Trypanosomes brucei. Beobachtungen und Experimente aus dem Kriege in Ostafrika. Arch. f. Schiffs- u. Trop.-Hyg. 23, 211.Google Scholar
Taylor, A. W. (1930). Experiments on the mechanical transmission of West African strains of Trypanosoma brucei and T. gambiense by Glossina and other biting flies. Trans. Roy. Soc. Trop. Med. and Hyg. 24, No. 3, pp. 289303.CrossRefGoogle Scholar
Van Hoof, L. and Henrard, C. (1933). La transmission cyclique de races résistantes d. Trypanosomes gambiense par Glossina palpalis. Ann. Soc. Belge de Méd. Trop. 13, 219.Google Scholar
Yorke, W. (1920). Research into the trypanosomiasis problem. Trans. Roy. Soc. Trop. Med. and Hyg. 15, 31.CrossRefGoogle Scholar
Yorke, W., Adams, A. R. D. and Murgatroyd, F. (1930). Studies in chemi-therapy. II. The action in vitro of normal human serum on the pathogenic trypanosomes, and its significance. Ann. Trop. Med. and Parasitol. 24, 115.CrossRefGoogle Scholar
Zimmermann, G. (1931). Ueber die trypanozide Wirkung des menschlichen Serums in Tier-versuch und in vitro. Zentralblatt f. Bakt. I, Orig. 120, 422.Google Scholar