Gönczöl E, Stone J, Melero J M
J Gen Virol. 1978 Jun;39(3):415-26. doi: 10.1099/0022-1317-39-3-415.
Heat-inactivated murine cytomegalovirus (MCMV) stimulates cellular DNA synthesis in WME, NMG, 3T3, WgIA, chick and NIK-8 cells, but active or u.v.-irradiated MCMV does not. The stimulation of DNA synthesis in NIL-8 and chick cells was studied in detail. We found that both the nuclear and the mitochondrial DNA synthesis were stimulated in these cells. There was no virus DNA synthesis during the period we studied (48 h). The stimulation of nuclear DNA synthesis was about threefold in NIL-8 and 2.5-fold in chick cells as measured by the rate of incorporation of 3H-thymidine (3H-dThd) in the CsCl fractions which banded at the density of cell DNA. The stimulation was about 9.5-fold in NIL-8 and 1.7-fold in chick cells as detected by autoradiography. There was a 3-fold and a 2.2-fold increase in the degree of incorporation of 3H-dThd into mitochondrial DNA of NIL-8 and chick cells, respectively. The amount of mitochondrial DNA obtained in infected cells of both kinds was about twice that in control cells. The synthesis of mitochondrial DNA was also stimulated by a factor of 2 in the thymidine kinaseless 3T3 cells which incorporate exogenous thymidine exclusively into mitochondrial DNA. There were no MCMV specific antigens detectable by immunofluorescence 5 h after infection, but diffuse nuclear fluorescence could be demonstrated 24 h after infection. Our results indicate that the heat-inactivated virus penetrates the cells, stimulates host DNA synthesis and induces synthesis of early MCMV antigens.
热灭活的鼠巨细胞病毒(MCMV)可刺激WME、NMG、3T3、WgIA、鸡和NIK - 8细胞中的细胞DNA合成,但活性或紫外线照射的MCMV则不能。我们详细研究了NIL - 8和鸡细胞中DNA合成的刺激情况。我们发现这些细胞中的核DNA和线粒体DNA合成均受到刺激。在我们研究的时间段(48小时)内没有病毒DNA合成。通过在密度与细胞DNA相同的CsCl组分中3H - 胸腺嘧啶核苷(3H - dThd)的掺入率来衡量,NIL - 8细胞中核DNA合成的刺激约为三倍,鸡细胞中约为2.5倍。通过放射自显影检测,NIL - 8细胞中的刺激约为9.5倍,鸡细胞中约为1.7倍。NIL - 8和鸡细胞中线粒体DNA中3H - dThd的掺入程度分别增加了3倍和2.2倍。两种感染细胞中获得的线粒体DNA量约为对照细胞中的两倍。在仅将外源性胸腺嘧啶核苷掺入线粒体DNA的无胸腺嘧啶激酶的3T3细胞中,线粒体DNA的合成也受到了2倍的刺激。感染后5小时通过免疫荧光无法检测到MCMV特异性抗原,但感染后24小时可显示弥漫性核荧光。我们的结果表明,热灭活病毒可穿透细胞,刺激宿主DNA合成并诱导早期MCMV抗原的合成。