Kaffashi Amir, Pagel Charles N, Noormohammadi Amir H, Browning Glenn F
Department of Poultry Viral Vaccine Prodution and Research, Razi Vaccine and Serum Research Institute, Karaj, Iran.
Department of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, 3010, Australia.
Arch Virol. 2015 Oct;160(10):2557-63. doi: 10.1007/s00705-015-2542-8. Epub 2015 Aug 2.
Although viral protein 3 (VP3) of chicken anaemia virus (CAV) has been well recognised as an inducer of apoptosis, viral protein 2 (VP2) of the virus has only been speculated to have apoptotic activity. This has not been verified because the open reading frame (ORF) encoding VP2 completely encompasses that encoding VP3, and thus the possibility of expression of VP3 cannot be excluded. The aim of this study was to elucidate the potential role of VP2 as an inducer of apoptosis. Site-directed mutagenesis was used to generate a point mutation that knocked out VP3 by early termination of its translation with a stop codon without imposing any change in the amino acid sequence of VP2. The mutated sequence was inserted into the pCAT plasmid preceded by a favorable Kozak's consensus sequence to create pCAT-VP2(+)VP3(-). The absence of VP3 expression in MSB1 cells transfected with this plasmid was confirmed using Western blotting, and DNA strand breaks and nuclear morphological changes were assessed to detect apoptosis. There was an increased level of apoptotic death in cells transfected with pCAT-VP2(+)VP3(-) compared to those transfected with the vector alone. This provides evidence that CAV VP2 can induce apoptosis.
虽然鸡贫血病毒(CAV)的病毒蛋白3(VP3)已被公认为凋亡诱导剂,但该病毒的病毒蛋白2(VP2)仅被推测具有凋亡活性。这一点尚未得到证实,因为编码VP2的开放阅读框(ORF)完全包含编码VP3的开放阅读框,因此无法排除VP3表达的可能性。本研究的目的是阐明VP2作为凋亡诱导剂的潜在作用。使用定点诱变产生一个点突变,通过提前终止其翻译并加入终止密码子来敲除VP3,同时不改变VP2的氨基酸序列。将突变序列插入到pCAT质粒中,其前面带有一个合适的科扎克共有序列,以构建pCAT-VP2(+)VP3(-)。使用蛋白质免疫印迹法证实了用该质粒转染的MSB1细胞中不存在VP3表达,并评估了DNA链断裂和细胞核形态变化以检测凋亡。与单独用载体转染的细胞相比,用pCAT-VP2(+)VP3(-)转染的细胞凋亡死亡水平有所增加。这提供了CAV VP2可诱导凋亡的证据。