Berens R L, Brun R, Krassner S M
J Parasitol. 1976 Jun;62(3):360-5.
An inexpensive, easily prepared monophasic medium which supports continuous culture of Leishmania donovanì (approximately 4 X 10(7) cells/ml/day 5) and L. tarentolae (approximately 3.5 X 10(7) cells/ml/day 5) promastigotes has been developed. This medium, designated HO-MEM, is a modified Eagle's minimal essential medium with Spinner's salts and 10% fetal calf serum. Epimastigotes of Trypanosoma cruzi, Costa Rica strain, also grew well in HO-MEM (approximately 2 X 10(7) cells/ml/day 5) but cells of the Corpus Christi strain grew poorly in the medium. The initial inoculum for all of the above culture systems was 3 X 10(5) cells which means that there was approximately 100-fold increase in cell number within 5 days of culture. Average doubling time for L. donovani in HO-MEM during log growth phase was 10 to 12 hr; this shortened to 9.25 hr at mid-log growth (day 2). The optimal pH range for L. donovani was 7.2 to 7.4 and optimal culture temperatures were 25 to 26 C. A change was seen in the average size distribution of L. donovani promastigotes during the growth cycle with smaller cells predominating each succeding day of culture. HO-MEM is a good medium for transformation of L. donovani amastigotes to promastigotes (60 to 80% in 48 hr).
已研制出一种廉价、易于制备的单相培养基,该培养基可支持杜氏利什曼原虫(约4×10⁷个细胞/毫升/天⁵)和热带利什曼原虫(约3.5×10⁷个细胞/毫升/天⁵)前鞭毛体的连续培养。这种培养基命名为HO - MEM,是一种添加了斯皮纳盐和10%胎牛血清的改良伊格尔最低必需培养基。克氏锥虫哥斯达黎加株的上鞭毛体在HO - MEM中也生长良好(约2×10⁷个细胞/毫升/天⁵),但科珀斯克里斯蒂株的细胞在该培养基中生长较差。上述所有培养系统的初始接种量均为3×10⁵个细胞,这意味着在培养5天内细胞数量增加了约100倍。杜氏利什曼原虫在HO - MEM中对数生长期的平均倍增时间为10至12小时;在对数生长期中期(第2天)缩短至9.25小时。杜氏利什曼原虫的最佳pH范围为7.2至7.4,最佳培养温度为25至26℃。在生长周期中,杜氏利什曼原虫前鞭毛体的平均大小分布发生了变化,随着培养天数的增加,较小的细胞占主导地位。HO - MEM是将杜氏利什曼原虫无鞭毛体转化为前鞭毛体的良好培养基(48小时内转化率为60%至80%)。