A rodent adapted clone of Trypanosoma vivax was used to infect cyclophosphamide treated mice and rats. Fresh blood containing trypanosomes, was centrifuged in a density gradient of three Percoll solutions, 1.07, 1.06, 1.05 g/ml, respectively, carefully layered on top of each other. The yields of this simple procedure for trypanosome purification were about six times higher than those obtained with the conventional anion-exchange columns. Cryopreservation of trypanosomes using glycerol yielded 90 % viable parasites, whereas using dimethylsulfoxide, a more commonly used cryoprotectant, the viability was only 35 %.
CITATION STYLE
Ndao, M., Magnus, E., Büscher, P., & Geerts, S. (2004). Trypanosoma vivax: A simplified protocol for in vivo growth, isolation and cryopreservation. Parasite, 11(1), 103–106. https://doi.org/10.1051/parasite/2004111103
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