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马立克氏病病毒的悬浮培养及其免疫效果评估。

Suspension culture of Marek's disease virus and evaluation of its immunological effects.

作者信息

Wen Lianghai, Zhang Aiguo, Li Yanpeng, Lai Hanzhang, Li Huimin, Luo Qiong, Jin Shuangxing, Chen Ruiai

机构信息

a College of Veterinary Medicine , South China Agricultural University , Guangzhou , People's Republic of China.

b Zhaoqing Institute of Biotechnology Co. Ltd. , Zhaoqing , People's Republic of China.

出版信息

Avian Pathol. 2019 Jun;48(3):183-190. doi: 10.1080/03079457.2018.1556385. Epub 2019 Apr 3.

Abstract

Marek's disease virus (MDV) is a cell-associated α-herpesvirus of chickens. It is difficult to grow MDV in suspension culture. Therefore, MDV vaccines are currently produced using adherent primary chicken embryo fibroblasts, and on a large scale this is labour-intensive and costly. In this study, the CVI988 strain of MDV was inoculated into chicken fibroblast cell line UMNSAH/DF-1 (DF-1) cultured by microcarrier suspension for the proliferation experiment. Moreover, the effects of culture conditions, such as inoculation method, multiplicity of infection (MOI), microcarrier concentration, and pH value, on the proliferation of MDV were investigated. The results demonstrated that the maximum viral load of 64.76 ± 2.64 × 10 PFU/flask in a working volume of 100 ml could be obtained using synchronous cell seeding and inoculation method at an MOI of 0.02 and a microcarrier concentration of 5 g/l at pH 7.2. At the same time, the CVI988/DF-1 vaccines prepared by the microcarrier culture process and the traditional adherent cell culture process (CVI988/Rispens) were compared through bird experiments. We found a protective rate of 94.4% using the CVI988/DF-1 vaccine with specific pathogen-free chickens that was equivalent to that of the commercial vaccine CVI988/Rispens (protection rate of 94.1%). In this study, the MDV CVI988/DF-1 vaccine prepared by the microcarrier suspension culture of DF-1 cells could provide effective immune protection for specific pathogen-free chickens, providing a reference for the prevention and control of MD and further development of a large-scale bioreactor for producing the MD vaccine.

摘要

马立克氏病病毒(MDV)是鸡的一种细胞相关α疱疹病毒。MDV在悬浮培养中难以生长。因此,目前MDV疫苗是使用贴壁的原代鸡胚成纤维细胞生产的,而大规模生产时这一过程劳动强度大且成本高昂。在本研究中,将MDV的CVI988株接种到通过微载体悬浮培养的鸡成纤维细胞系UMNSAH/DF-1(DF-1)中进行增殖实验。此外,还研究了接种方法、感染复数(MOI)、微载体浓度和pH值等培养条件对MDV增殖的影响。结果表明,在工作体积为100 ml时,采用同步细胞接种方法,MOI为0.02,微载体浓度为5 g/l,pH值为7.2,可获得最大病毒载量为64.76±2.64×10 PFU/瓶。同时,通过禽实验比较了微载体培养工艺制备的CVI988/DF-1疫苗和传统贴壁细胞培养工艺(CVI988/Rispens)制备的疫苗。我们发现,使用CVI988/DF-1疫苗对无特定病原体鸡的保护率为94.4%,与商业疫苗CVI988/Rispens的保护率(94.1%)相当。在本研究中,通过DF-1细胞微载体悬浮培养制备的MDV CVI988/DF-1疫苗可为无特定病原体鸡提供有效的免疫保护,为MD的防控及大规模生产MD疫苗的生物反应器的进一步开发提供参考。

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