CA-CAS-01-A:用于分离和开发非洲猪瘟病毒减毒活疫苗的易感细胞系。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-02-01 Epub Date: 2024-03-13 DOI:10.1007/s12275-024-00116-1
Seung-Chul Lee, Yongkwan Kim, Ji-Won Cha, Kiramage Chathuranga, Niranjan Dodantenna, Hyeok-Il Kwon, Min Ho Kim, Weonhwa Jheong, In-Joong Yoon, Joo Young Lee, Sung-Sik Yoo, Jong-Soo Lee
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引用次数: 0

摘要

非洲猪瘟病毒(ASFV)是影响家猪和野猪的高致命性非洲猪瘟的病原体。尽管该病毒在全球迅速传播,但目前还没有获得许可的疫苗。缺乏合适的 ASFV 繁殖细胞系阻碍了安全有效疫苗的开发。对于 ASFV 的繁殖,原代猪巨噬细胞和单核细胞已被广泛研究。然而,获取这些细胞既费时又昂贵,因此不适合大规模疫苗生产。本研究的目的是验证新型 CA-CAS-01-A (CAS-01) 细胞的适用性,CAS-01-A 被确定为 MA-104 亲本细胞系中对 ASFV 复制具有高度容许性的细胞克隆,可用于减毒活疫苗的开发。通过筛选实验,与 MA-104 的其他亚克隆相比,CAS-01 细胞中的 ASFV 复制量最大,Ct 值和 TCID50/ml 值分别为 14.89 和 log10 7.5 ± 0.15。当 CAS-01 细胞接种 ASFV 后,通过 ASFV DNA Ct 值、HAD50/ml 检测、TCID50/ml 检测证实了 ASFV 的复制,并观察到细胞病理效应和血细胞减少,与原代猪肺泡巨噬细胞第 5 次通过后的细胞病理效应和血细胞减少相似。此外,我们还证明了 ASFV 在连续培养过程中的稳定复制和适应性。这些结果表明,CAS-01 细胞将是一种有价值、有前景的细胞系,可用于 ASFV 的分离、复制和减毒活疫苗的开发。
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CA-CAS-01-A: A Permissive Cell Line for Isolation and Live Attenuated Vaccine Development Against African Swine Fever Virus.

African swine fever virus (ASFV) is the causative agent of the highly lethal African swine fever disease that affects domestic pigs and wild boars. In spite of the rapid spread of the virus worldwide, there is no licensed vaccine available. The lack of a suitable cell line for ASFV propagation hinders the development of a safe and effective vaccine. For ASFV propagation, primary swine macrophages and monocytes have been widely studied. However, obtaining these cells can be time-consuming and expensive, making them unsuitable for mass vaccine production. The goal of this study was to validate the suitability of novel CA-CAS-01-A (CAS-01) cells, which was identified as a highly permissive cell clone for ASFV replication in the MA-104 parental cell line for live attenuated vaccine development. Through a screening experiment, maximum ASFV replication was observed in the CAS-01 cell compared to other sub-clones of MA-104 with 14.89 and log10 7.5 ± 0.15 Ct value and TCID50/ml value respectively. When CAS-01 cells are inoculated with ASFV, replication of ASFV was confirmed by Ct value for ASFV DNA, HAD50/ml assay, TCID50/ml assay, and cytopathic effects and hemadsoption were observed similar to those in primary porcine alveolar macrophages after 5th passage. Additionally, we demonstrated stable replication and adaptation of ASFV over the serial passage. These results suggest that CAS-01 cells will be a valuable and promising cell line for ASFV isolation, replication, and development of live attenuated vaccines.

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