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在微载体上培养用于生产四血清型登革病毒的蚊子和哺乳动物细胞:病毒滴度、蚀斑形态和复制速率的变化

Mosquito and mammalian cells grown on microcarriers for four-serotype dengue virus production: variations in virus titer, plaque morphology, and replication rate.

作者信息

Liu Chia-Chyi, Wu Suh-Chin

机构信息

Institute of Biotechnology and Department of Life Science, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

Biotechnol Bioeng. 2004 Mar 5;85(5):482-8. doi: 10.1002/bit.10918.

Abstract

Dengue (DEN) viruses consisting of four distinct serotypes cause diseases such as dengue fever, dengue hemorrhagic fever, and dengue shock syndrome in humans. Most of the dengue viruses can be effectively propagated in some mosquito and mammalian cell lines. In this study, we applied microcarrier cell culture technology to study two relevant aspects involving dengue virus, one on biotechnology of cell growth and virus production, and the other on virus biology concerning genetic variation of a virus population. We investigated the growth of C6/36 mosquito cells and Vero cells grown on Cytodex 1 microcarriers. High-titer DEN virus production can be achieved in C6/36 and Vero cells infected at low cell inoculation density, in the lag-phase cell stage, and at low multiplicity of infection (MOI). The maximum titers produced for DEN-1, DEN-3, and DEN-4 viruses were approximately 10- to 10,000-fold lower than for DEN-2 virus produced in C6/36 and Vero cells grown on microcarriers. The DEN-2 virus produced in C6/36 cells displayed far more extensive plaque heterogeneity than in Vero cells. Microcarrier C6/36 mosquito cell culture appeared to be the most effective system for four-serotype DEN virus production. Interestingly, some selected variants of DEN virus may outgrow in Vero cells when using a T-flask culture. These results may provide useful information for DEN vaccine development.

摘要

登革热(DEN)病毒由四种不同血清型组成,可导致人类患上登革热、登革出血热和登革休克综合征等疾病。大多数登革热病毒能在某些蚊子和哺乳动物细胞系中有效增殖。在本研究中,我们应用微载体细胞培养技术来研究登革热病毒相关的两个方面,一方面是细胞生长和病毒生产的生物技术,另一方面是关于病毒群体遗传变异的病毒生物学。我们研究了在Cytodex 1微载体上生长的C6/36蚊子细胞和Vero细胞的生长情况。在低细胞接种密度、对数生长期细胞阶段以及低感染复数(MOI)条件下感染的C6/36和Vero细胞中,可实现高滴度登革热病毒的生产。在微载体上生长的C6/36和Vero细胞中产生的DEN-1、DEN-3和DEN-4病毒的最大滴度比DEN-2病毒低约10至10000倍。在C6/36细胞中产生的DEN-2病毒比在Vero细胞中表现出更广泛的蚀斑异质性。微载体C6/36蚊子细胞培养似乎是生产四血清型登革热病毒最有效的系统。有趣的是,当使用T型瓶培养时,一些选定的登革热病毒变体可能在Vero细胞中生长得更好。这些结果可能为登革热疫苗的开发提供有用信息。

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