Department of Mechanical Engineering, University of Washington, Seattle, Washington, USA.
J Clin Microbiol. 2012 Nov;50(11):3575-80. doi: 10.1128/JCM.00896-12. Epub 2012 Aug 29.
Successful long-term preservation of Mycobacterium tuberculosis cells is important for sample transport, research, biobanking, and the development of new drugs, vaccines, biomarkers, and diagnostics. In this report, Mycobacterium bovis bacillus Calmette-Guérin and M. tuberculosis H37Ra were used as models of M. tuberculosis complex strains to study cryopreservation of M. tuberculosis complex cells in diverse sample matrices at different cooling rates. Cells were cryopreserved in diverse sample matrices, namely, phosphate-buffered saline (PBS), Middlebrook 7H9 medium with or without added glycerol, and human sputum. The efficacy of cryopreservation was quantified by microbiological culture and microscopy with BacLight LIVE/DEAD staining. In all sample matrices examined, the microbiological culture results showed that the cooling rate was the most critical factor influencing cell viability. Slow cooling (a few degrees Celsius per minute) resulted in much higher M. tuberculosis complex recovery rates than rapid cooling (direct immersion in liquid nitrogen) (P < 0.05). Among the three defined cryopreservation media (PBS, 7H9, and 7H9 plus glycerol), there was no significant differential effect on viability (P = 0.06 to 0.87). Preincubation of thawed M. tuberculosis complex cells in 7H9 broth for 20 h before culture on solid Middlebrook 7H10 plates did not help the recovery of the cells from cryoinjury (P = 0.14 to 0.71). The BacLight LIVE/DEAD staining kit, based on Syto 9 and propidium iodide (PI), was also applied to assess cell envelope integrity after cryopreservation. Using the kit, similar percentages of "live" cells with intact envelopes were observed for samples cryopreserved under different conditions, which was inconsistent with the microbiological culture results. This implies that suboptimal cryopreservation might not cause severe damage to the cell wall and/or membrane but instead cause intracellular injury, which leads to the loss of cell viability.
成功地长期保存结核分枝杆菌细胞对于样本运输、研究、生物库以及新药物、疫苗、生物标志物和诊断方法的开发都很重要。在本报告中,牛分枝杆菌卡介苗和 H37Ra 被用作结核分枝杆菌复合群菌株的模型,以研究在不同冷却速率下不同样本基质中结核分枝杆菌复合群细胞的冷冻保存。细胞在不同的样本基质中进行冷冻保存,包括磷酸盐缓冲盐水(PBS)、含或不含甘油的 Middlebrook 7H9 培养基以及人痰。通过微生物培养和 BacLight LIVE/DEAD 染色的显微镜检查来量化冷冻保存的效果。在所有检查的样本基质中,微生物培养结果表明,冷却速率是影响细胞活力的最关键因素。与快速冷却(直接浸入液氮中)相比,缓慢冷却(每分钟几度)导致结核分枝杆菌复合群的回收效率更高(P < 0.05)。在三种定义的冷冻保存培养基(PBS、7H9 和 7H9 加甘油)中,对活力没有明显的差异影响(P = 0.06 至 0.87)。在将解冻的结核分枝杆菌复合群细胞预孵育在 7H9 肉汤中 20 小时后,再在固体 Middlebrook 7H10 平板上进行培养,这对从冷冻损伤中恢复细胞没有帮助(P = 0.14 至 0.71)。基于 Syto 9 和碘化丙啶(PI)的 BacLight LIVE/DEAD 染色试剂盒也用于评估冷冻保存后细胞包膜的完整性。使用该试剂盒,观察到在不同条件下冷冻保存的样本中具有完整包膜的“活”细胞的比例相似,这与微生物培养结果不一致。这意味着次优的冷冻保存可能不会对细胞壁和/或膜造成严重损伤,而是导致细胞内损伤,从而导致细胞活力丧失。