Maraghi S, Wallbanks K R, Molyneux D H, Abdel-Hafez S K
Department of Medical Parasitology and Mycology, Medical School, University of Medical Sciences, Ahwaz, Iran.
Parasitol Res. 1995;81(8):672-6. doi: 10.1007/BF00931845.
When Trypanosoma acomys bloodstream forms were cultivated at 37 degrees C in Schneider's Drosophila medium supplemented with 20% (v/v) heat-inactivated foetal calf serum (FCS), with Microtus agrestis embryonic fibroblasts in RPMI 1640 medium supplemented with 20% FCS or in Baltz's medium supplemented with 10% FCS, the parasites transformed and largely remained as epimastigotes. Epimastigotes were also usually the commonest stage observed when the parasites were co-cultivated with a mosquito cell line at 27 degrees C. However, if these cultures were initiated with the supernatant suspensions from fibroblast cultures that had been cryopreserved, trypomastigotes, including bloodstream-like forms, were the predominant stage for the first 4 days of culture. It is suggested that the glycerol supplement or the temperature changes stimulated this unusual morphogenesis. At 27 degrees C, T. acomys was incapable of multiplying and died when cultured in fresh Schneider's Drosophila medium supplemented with 20% FCS, but co-cultivation with the mosquito cell lines or cultivation in cell-free supernatants from 1-week-old mosquito cell cultures was successful at this temperature; most of the parasites multiplied as epimastigotes.
当将刚毛鼠锥虫的血流型在补充有20%(v/v)热灭活胎牛血清(FCS)的施耐德果蝇培养基中于37℃培养,或在补充有20% FCS的RPMI 1640培养基中与田鼠胚胎成纤维细胞共培养,或在补充有10% FCS的巴尔茨培养基中培养时,寄生虫发生转化并大多保持为上鞭毛体。当寄生虫在27℃与蚊细胞系共培养时,上鞭毛体通常也是最常见的阶段。然而,如果这些培养物用已冷冻保存的成纤维细胞培养物的上清液悬浮液起始培养,包括类血流型在内的锥鞭毛体在前4天的培养中是主要阶段。提示甘油补充剂或温度变化刺激了这种异常的形态发生。在27℃时,刚毛鼠锥虫在补充有20% FCS的新鲜施耐德果蝇培养基中培养时无法增殖并死亡,但在此温度下与蚊细胞系共培养或在1周龄蚊细胞培养物的无细胞上清液中培养成功;大多数寄生虫以上鞭毛体形式增殖。