Department of Microbiology, University of Kansas Medical Center, Kansas City, KS, USA.
Virology. 2010 Aug 1;403(2):145-54. doi: 10.1016/j.virol.2010.04.014. Epub 2010 May 10.
We have generated a quantitative transcription profile of human bocavirus type 1 (HBoV1) by transfecting a nearly full-length clone in human lung epithelial A549 cells as well as in a replication competent system in 293 cells. The overall transcription profile of HBoV1 is similar to that of two other members of genus Bocavirus, minute virus of canines and bovine parvovirus 1. In particular, a spliced NS1-transcript that was not recognized previously expressed the large non-structural protein NS1 at approximately 100kDa; and the NP1-encoding transcripts were expressed abundantly. In addition, the protein expression profile of human bocavirus type 2 (HBoV2) was examined in parallel by transfection of a nearly full-length clone in A549 cells, which is similar to that of HBoV1. Moreover, our results showed that, unlike human parvovirus B19 infection, expression of the HBoV1 proteins only does not induce cell cycle arrest and apoptosis of A549 cells.
我们通过转染人肺上皮 A549 细胞中的近乎全长克隆以及在 293 细胞中的复制有效系统,生成了人博卡病毒 1 型(HBoV1)的定量转录谱。HBoV1 的整体转录谱与其他两种细小病毒属成员,犬细小病毒和牛细小病毒 1 的转录谱相似。特别是,以前未被识别的拼接 NS1-转录本表达了大约 100kDa 的大非结构蛋白 NS1;并且 NP1 编码的转录本大量表达。此外,我们通过在 A549 细胞中转染近乎全长克隆平行检测了人博卡病毒 2 型(HBoV2)的蛋白表达谱,这与人博卡病毒 1 型相似。此外,我们的结果表明,与人类细小病毒 B19 感染不同,HBoV1 蛋白的表达不会导致 A549 细胞的细胞周期停滞和凋亡。