Hirumi H, Hirumi K, Doyle J J, Cross G A
Parasitology. 1980 Apr;80(2):371-82. doi: 10.1017/s0031182000000822.
Clones of animal-infective bloodstream forms of Trypanosoma brucei (stocks S.427 and LUMP 227) were made by transferring a single organism from bloodstream-form cultures into each well of Microtest II Tissue Culture Plates containing bovine fibroblast-like feeder cells. When the number of trypanosomes increased to 10(2)--10(3)/well on days 4--16, they were transferred into plastic T-25 culture flasks also containing feeder cells and fresh medium. Cultures were thereafter maintained by partially replacing the trypanosome suspension with the same volume of fresh medium (diluting the density to 2--5 x 15(5) trypanosomes/ml) every 24 h. Sub-cultivations could be made by transferring 1--2 ml of the trypanosome suspension to a new culture flask at 4--5 day intervals. A total of 42 clones in the 3 series TC221, TC52 and TC227, carrying variable antigen types (VATs) 221, 052 and ILTat 1.4, respectively, have been established. Average population doubling times for clones of TC221, TC52 and TC227 were 8.7, 14.5 and 15.5 h respectively. Of 35 populations examined, 34 clones retained the original specificity of their VATs for at least 8--32 days from cloning. One cloned population of TC52 consisted of 99.8% VAT 052 and 0.2% VAT 221 at the time when the first VAT test was made on day 18.
通过将布氏锥虫动物感染性血流形式的单个生物体(菌株S.427和LUMP 227)从血流形式培养物转移到含有牛成纤维细胞样饲养细胞的微量试验II组织培养板的每个孔中,制备了克隆。当锥虫数量在第4至16天增加到每孔10² - 10³个时,将它们转移到同样含有饲养细胞和新鲜培养基的塑料T - 25培养瓶中。此后,通过每24小时用相同体积的新鲜培养基部分替换锥虫悬液(将密度稀释至2 - 5×10⁵个锥虫/毫升)来维持培养。每隔4 - 5天将1 - 2毫升锥虫悬液转移到新的培养瓶中进行传代培养。总共建立了3个系列TC221、TC52和TC227中的42个克隆,分别携带可变抗原类型(VATs)221、052和ILTat 1.4。TC221、TC52和TC227克隆的平均群体倍增时间分别为8.7小时、14.5小时和15.5小时。在检测的35个群体中,34个克隆从克隆起至少8 - 32天保持其VATs的原始特异性。在第18天进行首次VAT检测时,TC52的一个克隆群体由99.8%的VAT 052和0.2%的VAT 221组成。