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建立胡萝卜 SMC-1 细胞悬浮系用于脊髓灰质炎疫苗的开发。

Establishment of the Daucus carota SMC-1 Cell Suspension Line for Poliovirus Vaccine Development.

机构信息

Centro de Investigación en Biotecnología, Universidad Autónoma del Estado de Morelos, Cuernavaca, Morelos, Mexico.

Laboratorio de Biofarmacéuticos Recombinantes, Universidad Autónoma de San Luis Potosí, SLP, Mexico.

出版信息

Planta Med. 2024 Jan;90(1):63-72. doi: 10.1055/a-2181-2886. Epub 2023 Oct 18.

Abstract

The development of virus-free, oral vaccines against poliovirus capable of inducing mucosal protective immunity is needed to safely combat this pathogen. In the present study, a carrot cell line expressing the poliovirus VP2 antigen was established at the level of callus and cell suspensions, exploring the effects of culture media (MS and B5), supplementation with urea, phytoregulators (2,4-D : KIN), and light conditions (continuous light, photoperiod, and total darkness). The best callus growth was obtained on B5 medium supplemented with 2 mg/L of 2,4-D + 2 mg/L kinetin and 0.0136 g/L of urea and in continuous light conditions. Suspension cultures of the SMC-1 line in 250 mL Erlenmeyer flasks had a maximum growth of 16.07 ± 0.03 g/L DW on day 12 with a growth rate of µ=0.3/d and a doubling time of 2.3 days. In a 2 L airlift bioreactor, the biomass yield achieved was 25.6 ± 0.05 g/L DW at day 10 with a growth rate of µ= 0.58/d and doubling time of 1.38 d. Cell growth was 1.5 times higher in bioreactors than in shake flasks, highlighting that both systems resulted in the accumulation of VP2 throughout the time in culture. The maximum VP2 yield in flasks was 387.8 µg/g DW at day 21, while in the reactor it was 550.2 µg/g DW at day 18. In conclusion, bioreactor-based production of the VP2 protein by the SMC-1 suspension cell line offers a higher productivity when compared to flask cultures, offering a key perspective to produce low-cost vaccines against poliomyelitis.

摘要

需要开发无病毒、口服的脊髓灰质炎病毒疫苗,以诱导黏膜保护性免疫,从而安全地对抗这种病原体。在本研究中,在愈伤组织和细胞悬浮液水平上建立了表达脊髓灰质炎病毒 VP2 抗原的胡萝卜细胞系,探索了培养基(MS 和 B5)、添加尿素、植物调节剂(2,4-D:KIN)和光照条件(连续光照、光周期和完全黑暗)的影响。在补充 2 mg/L 2,4-D+2 mg/L 激动素和 0.0136 g/L 尿素的 B5 培养基和连续光照条件下,获得了最佳的愈伤组织生长。SMC-1 系的悬浮培养在 250 mL Erlenmeyer 摇瓶中于第 12 天以最大生长量 16.07±0.03 g/L DW 生长,生长速率µ=0.3/d,倍增时间为 2.3 天。在 2 L 气升式生物反应器中,第 10 天达到的生物量产量为 25.6±0.05 g/L DW,生长速率µ=0.58/d,倍增时间为 1.38 d。与摇瓶相比,生物反应器中的细胞生长速度提高了 1.5 倍,这突出表明两个系统在整个培养过程中都导致 VP2 的积累。摇瓶中的最大 VP2 产量在第 21 天达到 387.8 µg/g DW,而在反应器中在第 18 天达到 550.2 µg/g DW。总之,SMC-1 悬浮细胞系在生物反应器中生产 VP2 蛋白的产量比摇瓶培养更高,为生产低成本脊髓灰质炎疫苗提供了一个关键视角。

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