Takahashi T, Ozawa K, Takahashi K, Okuno Y, Takahashi T, Muto Y, Takaku F, Asano S
Department of Hematology-Oncology, Institute of Medical Science, University of Tokyo, Japan.
Arch Virol. 1993;131(1-2):201-8. doi: 10.1007/BF01379092.
A major limitation of studies on the parvovirus B 19, a causative agent of transient aplastic crisis, has been the absence of appropriate cell lines permissive for the virus. In the present study, a human erythroid leukemia cell line (JK-1) was shown to support B 19 virus DNA replication in vitro. Forty-eight hours after virus inoculation of JK-1 liquid cell cultures, the average number of B 19 genome copies was estimated at 3,000 per cell by DNA dot blot analysis. The addition of erythropoietin increased B 19 copy number to 10,000 per cell. The presence of replicative forms of the B 19 virus genome was genome was demonstrated by Southern blot analysis. Although persistent infection of B 19 virus was not observed in JK-1 cells, this culture system will be of value in elucidating the molecular basis of the erythroid specificity of parvovirus B 19.
作为暂时性再生障碍危象病原体的细小病毒B19,其研究的一个主要局限在于缺乏对该病毒具有易感性的合适细胞系。在本研究中,一种人类红白血病细胞系(JK-1)被证明能够在体外支持B19病毒的DNA复制。将病毒接种到JK-1液体细胞培养物中48小时后,通过DNA斑点印迹分析估计,每个细胞中B19基因组拷贝的平均数量为3000个。添加促红细胞生成素后,B19拷贝数增加到每个细胞10000个。通过Southern印迹分析证实了B19病毒基因组复制形式的存在。尽管在JK-1细胞中未观察到B19病毒的持续感染,但该培养系统对于阐明细小病毒B19红系特异性的分子基础将具有重要价值。