在无血清培养基中培养MDCK细胞用于流感病毒生产的适宜性

N Kessler, G Thomas-Roche, L Gérentes, M Aymard
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引用次数: 0

摘要

使用Ultra-MDCK培养基(BioWHITTAKER), MDCK细胞已适应在无血清环境中生长。适应U-MDCK细胞的生长维持一年以上,细胞的生长速度没有下降,核型也没有改变;使用几个微载体将细胞扩大到旋转培养。无论在感染培养基中是否存在胰蛋白酶,这些细胞都是a型和B型流感病毒复制的良好宿主。不依赖胰蛋白酶的病毒在没有胰蛋白酶的连续传代中筛选后,在U-MDCK细胞中复制到高滴度(10(7)-10(8)TCID50/ml)。与用胰蛋白酶培养的标准病毒相比,该病毒后代表现出不裂解和抗原修饰的血凝素。最后,在微载体上培养的U-MDCK细胞中,在棒搅拌条件下,使用选定的胰蛋白酶独立变体产生了大量甲型和乙型流感病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Suitability of MDCK cells grown in a serum-free medium for influenza virus production.

MDCK cells have been adapted to grow in a serum-free environment using Ultra-MDCK medium (BioWHITTAKER). The growth of adapted U-MDCK cells was maintained for over a year without any reduction in growth rate or modification of cell karyotype; cells were scaled up to spinner culture using several microcarriers. The cells were shown to be a very good host for influenza A and B virus replication in both the presence and absence of trypsin in the infection medium. Trypsin-independent viruses replicated to high titres (10(7)-10(8) TCID50/ml) in U-MDCK cells, after selection through serial passages without trypsin. This virus progeny exhibited uncleaved and antigenically modified haemagglutinin compared with standard viruses grown with trypsin. Finally, large amounts of influenza A and B viruses were produced in U-MDCK cells grown on microcarriers under rod-stirred conditions using selected trypsin-independent variants.

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