Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-18T22:16:55.269Z Has data issue: false hasContentIssue false

Simultaneous presence of different antigenic populations of Trypanosoma brucei gambiense in Microtus montanus

Published online by Cambridge University Press:  06 April 2009

John Richard Seed
Affiliation:
Laboratory of Parasitology, Department of Biology, Tulane University, New Orleans, La. 70118, U.S.A.
Harris Gregory Effron
Affiliation:
Laboratory of Parasitology, Department of Biology, Tulane University, New Orleans, La. 70118, U.S.A.

Extract

Trypanosomes were isolated before and after the formation of infected detectable antibody from various brain sites and the blood of Microtus montanus. All isolates were serotyped by the agglutination reaction, and the isolates obtained prior to antibody formation were serologically identical to the original inoculum. Later isolates obtained from separate sites of an infected animal were serologically different from the original inoculum and also from each other. It was therefore concluded that in a single chronically infected animal there are numerous different antigenic populations of trypanosomes each occupying separate brain sites. A hypothesis to account for this antigenic diversity is given.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1973

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

Cunningham, M. P., & Vickerman, K., (1962). Antigenic analysis in the Trypanosoma brucei group, using the agglutination reaction. Transactions of the Royal Society of Tropical Medicine and Hygiene 56, 4859.CrossRefGoogle ScholarPubMed
McNeillage, G. J. C., Herbert, W. J., & Lumsden, W. H. R., (1969). Antigenic type of first relapse variants arising from a strain of Trypanosoma (Trypanozoon) brucei. Experimental Parasitology 25, 17.Google Scholar
Ormerod, W. E., & Venkatesan, S., (1971a). An amastigote phase of the sleeping sickness trypanosome. Transactions of the Royal Society of Tropical Medicine and Hygiene 65, 736–41.CrossRefGoogle ScholarPubMed
Ormerod, W. E., & Venkatesan, S., (1971b). The occult visceral phase of mammalian trypanosomes with special reference to the life cycle of Trypanosoma (Trypanozoon) brucei. Transactions of the Royal Society of Tropical Medicine and Hygiene 65, 722–35.CrossRefGoogle Scholar
Seed, J. R., (1963). The characterization of antigens isolated from Trypanosoma rhodesiense. Journal of Protozoology 10, 380–9.CrossRefGoogle ScholarPubMed
Seed, J. R., Baquero, M. A., & Duda, J. F., (1965). Inhibition of hexose and glycerol utilization by 2-deoxy-D-glucose in Trypanosoma gambiense and Trypanosoma rhodesiense. Experimental Parasitology 16, 363–8.CrossRefGoogle ScholarPubMed
Seed, J. R., & Gam, A. A., (1966). Passive immunity to experimental trypanosomiasis. Journal of Parasitology 52, 1134–40.CrossRefGoogle ScholarPubMed
Seed, J. R., & Khalili, N., (1971). The changes in locomotor rhythms of Mierotus montanus infected with Trypanosoma gambiense. Journal of Interdisciplinary Cycle Research 2, 91–9.Google Scholar
Seed, J. R., & Negus, N. G., (1970). Susceptibility of Microtus montanus to infection by Trypanosoma gambiense. Laboratory Animal Care 20, 657–61.Google Scholar
Soltys, M. A., & Woo, P., (1970). Further studies on tissue forms of Trypanosoma brucei in a vertebrate host. Transactions of the Royal Society of Tropical Medicine and Hygiene 64, 692–4.Google Scholar