The Effect of Lethal, Whole-Body Irradiation of Mice on Trypanosoma vivax Infection

Gee, A.L.W. de; Shah, Smruti D.

doi:10.2307/3280422

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“…The physiological changes brought about by sublethal irradiation of the rodents would appear to have facilitated adaptation ofthe two T. vivax stocks for growth in laboratory rodents. Whole-body irradiation has been used to aggravate African trypanosomiasis in experimental animals (3,15,23) and to establish West African T. vivax in rodents (10). De Gee (10) demonstrated that the effect of irradiation on the development of parasitemia in mice was variable depending on the T. vivax stabilate used and that irradiation influenced the physiology of the host in such a manner that the multiplication rate of certain trypanosome variants was either depressed or increased.…”

Section: Discussionmentioning

confidence: 99%

Trypanosoma vivax: Adaptation of Two East African Stocks to Laboratory Rodents1

Gathuo

Nantulya

Gardiner

1987

The Journal of Protozoology

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Two Trypanosoma vivax stocks from East Africa have been adapted to rats and mice. Adaptation was induced by rapid passage at two- to four-day intervals in sublethally irradiated rats. After 200 such passages, the two stocks gave rise to parasitemias of 10(9)-10(10) trypanosomes/ml in peripheral blood, and the infection was fatal in 90% of the rats. By passaging the rat-adapted T. vivax into normal mice at two- to three-day intervals for over 200 passages, the two stocks also became pathogenic to mice. One of the stocks was also capable of maintenance in non-irradiated rats. The two stocks displayed a marked degree of pleomorphism in irradiated and non-irradiated rats and mice. In the early rising parasitemia, the organisms were predominantly short, with a well formed undulating membrane, a pointed posterior end, and a large terminal kinetoplast. As parasitemia approached its peak, the organisms transformed into long, slender forms with an inconspicuous undulating membrane, an elongated posterior end, and a sub-terminal kinetoplast. The short forms associated with the early, rising parasitemia were more infective for mice than the long forms encountered at peak parasitemia. Although the two rodent-adapted stocks retained their pathogenicity for goats, neither the original stocks nor their corresponding rodent-adapted stocks could be cyclically transmitted by tsetse flies. The availability of these stocks will greatly facilitate investigations on East African T. vivax which would otherwise be difficult to carry out in experimental rodents.

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Section: Discussionmentioning

confidence: 99%