Schwegmann-Weßels Christel, Glende Jörg, Ren Xiaofeng, Qu Xiuxia, Deng Hongkui, Enjuanes Luis, Herrler Georg
Institute of Virology, University of Veterinary Medicine Hannover, Hannover, Germany.
College of Veterinary Medicine, Northeast Agricultural University, 59 Mucai Street, 150030 Harbin, PR China.
J Gen Virol. 2009 Jul;90(Pt 7):1724-1729. doi: 10.1099/vir.0.009704-0. Epub 2009 Mar 4.
The surface proteins S of severe acute respiratory syndrome coronavirus (SARS-CoV) and transmissible gastroenteritis virus (TGEV) were compared for their ability to mediate infection of viral pseudotypes based on vesicular stomatitis virus (VSV). The cell tropism of the respective pseudotypes corresponded to the tropism of the viruses from which the S protein was derived. Higher infectivity values were obtained with the SARS-CoV S protein than with the TGEV S protein. Differences were observed with respect to the importance of the cytoplasmic tail and the membrane anchor of the S proteins. In the case of the SARS-CoV S protein, truncation of the cytoplasmic tail resulted in increased infectivity. For the TGEV S protein, the inactivation of an intracellular retention signal in the cytoplasmic tail was required. Exchange of the membrane anchor of the S proteins led to a low infection efficiency. Our results indicate that related glycoproteins may show substantial differences in their ability to mediate pseudotype infection.
对严重急性呼吸综合征冠状病毒(SARS-CoV)和传染性胃肠炎病毒(TGEV)的表面蛋白S介导基于水疱性口炎病毒(VSV)的病毒假型感染的能力进行了比较。各自假型的细胞嗜性与S蛋白来源病毒的嗜性相对应。与TGEV S蛋白相比,SARS-CoV S蛋白获得了更高的感染性值。在S蛋白的细胞质尾巴和膜锚定的重要性方面观察到差异。就SARS-CoV S蛋白而言,细胞质尾巴的截断导致感染性增加。对于TGEV S蛋白,需要使细胞质尾巴中的细胞内保留信号失活。S蛋白膜锚定的交换导致感染效率低下。我们的结果表明,相关糖蛋白在介导假型感染的能力上可能存在显著差异。