Bhattacharya J, Chandra G, Hati A K
Department of Medical Entomology, Calcutta School of Tropical Medicine.
Indian J Med Res. 1991 Jul;93:245-6.
Cryopreservation of promastigotes of L. donovani in NNN and Tobie's media was attempted. The media containing the promastigotes were kept directly at -80 degrees C. The cryopreserved media were examined for living promastigotes after 9, 12, 15, 20, 23, 26, 29, 32, 42, 56, 65 and 126 days after the culture tubes were brought directly from -80 degrees C to room temperature and examined after 30 min. All tubes showed living promastigotes which were used for further growth with no apparent morphological changes in subsequent subcultures. Viability was optimum. This method of short term cryopreservation is simple, reliable and reproducible for cryopreservation of culture adapted parasites and also important because different strains can be stocked without using any other chemical, or special equipment and liquid nitrogen chamber, for further use in immunological or other purposes.
尝试在NNN培养基和托比培养基中对杜氏利什曼原虫前鞭毛体进行冷冻保存。含有前鞭毛体的培养基直接置于-80℃。在培养管从-80℃直接转移至室温并在30分钟后进行检查后,在9、12、15、20、23、26、29、32、42、56、65和126天对冷冻保存的培养基进行活前鞭毛体检查。所有培养管均显示有活的前鞭毛体,这些前鞭毛体用于进一步培养,在随后的传代培养中没有明显的形态变化。活力最佳。这种短期冷冻保存方法对于适应培养的寄生虫的冷冻保存而言简单、可靠且可重复,并且也很重要,因为无需使用任何其他化学物质、特殊设备或液氮罐就可以保存不同菌株,以便进一步用于免疫学或其他目的。