| 摘要: |
| 采用微型生物反应器确定纸片载体上F81细胞最佳的接种密度和最佳接毒剂量,在NBS反应器中验证温度对犬细小病毒YA-16-C66株增殖的影响。经过三次重复试验,确定利用NBS生物反应器培养犬细小病毒YA-16-C66株最佳工艺为：采用同步接毒法,培养基为含1%新生牛血清的199溶液,细胞接种密度为1.5×107cells/g,接毒剂量为0.05 MOI,在pH7.2条件下,37.0℃培养48h后降温到35.0℃继续培养24-48小时,细胞病变达到80%~90%时收获上清液。三批次反应器与转瓶工艺产品比较,结果表明：反应器比转瓶收获液病毒含量高1.1~1.9 lg TCID50/100μL；相同培养面积,反应器所得病毒总量是转瓶所得病毒总量的2.8-18.5倍。 |
| 关键词: 犬细小病毒 生物反应器 纸片载体 转瓶 培养工艺 |
| DOI： |
| 投稿时间：2020-07-24修订日期：2020-11-30 |
| 基金项目: |
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| Optimization of Flake disks culture of Canine Parvovirus YA-16-C66 strain and Comparative analysis of its culture technology with spinner bottle |
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| (Tangshan Yian Biological Engineering Co. Ltd) |
| Abstract: |
| The optimal inoculation density and dose of F81 cells on Flake disks were determined in a mini-bioreactor, and the effect of temperature on the proliferation of YA-16-C66 strain of Canine Parvovirus was verified in the NBS reactor. After three time of repeated experiments,the optimal culture process for the cultivation of YA-16-C66 strain of Canine Parvovirus by NBS bioreactor was determined:In the synchronous inoculation method, the culture medium was 199 solution containing 1% newborn bovine serum, the cell inoculation density was 1.5×107cells/g, and the inoculation dose was 0.05 MOI. Under the condition of pH7.2, the cells were cultured at 37.0℃ for 48h, then the temperature was lowered to 35.0℃ for 24-48 hours, and the supernatant was harvested when the cytopathod reached 80%~90%. The results showed that the virus content in the reactor was 1.1~1.9 lg TCID50/100 μL higher than that in the reactant. With the same culture area, the total amount of virus obtained from the reactor was 2.8-18.5 times that of the total amount of virus obtained from the spinner bottle. |
| Key words: Canine Parvovirus Bioreactor flake disks spinner bottle cultivation process |
