Damaso C R, Keller S J
Department of Biological Sciences, University of Cincinnati, Ohio.
Arch Virol. 1994;134(3-4):303-19. doi: 10.1007/BF01310569.
The effect of the immune modulator, Cyclosporin A (CsA) on vaccinia virus replication has been examined in cell cultures. In the present study we report that CsA is anti-viral towards vaccinia virus. Viral yield was inhibited by more than 97% after 24 h postinfection in the presence of 16 microM to 40 microM CsA. An analysis of the infectious cycle in greater detail revealed that CsA did not effect the total level of [35S] methionine incorporation into vaccinia infected cells. However, both early and late viral gene expression were inhibited by CsA. Late viral protein synthesis appeared to be more sensitive to the drug. At least one late viral polypeptide of approximately Mr 38,000 was virtually undetected up to 8 h postinfection in the presence of 40 microM CsA. Host protein synthesis which is normally inhibited by the virus was not turned off until very late in infection. Viral DNA replication was also inhibited by the addition of CsA at levels comparable to those observed for late protein synthesis.
免疫调节剂环孢菌素A(CsA)对痘苗病毒复制的影响已在细胞培养中进行了研究。在本研究中,我们报告CsA对痘苗病毒具有抗病毒作用。在感染后24小时,当存在16微摩尔至40微摩尔的CsA时,病毒产量受到超过97%的抑制。对感染周期更详细的分析表明,CsA并不影响[35S]甲硫氨酸掺入痘苗感染细胞的总量。然而,早期和晚期病毒基因表达均受到CsA的抑制。晚期病毒蛋白合成似乎对该药物更敏感。在存在40微摩尔CsA的情况下,直到感染后8小时,至少一种约38000道尔顿的晚期病毒多肽实际上未被检测到。通常被病毒抑制的宿主蛋白合成直到感染后期才被关闭。添加CsA对病毒DNA复制的抑制水平与观察到的晚期蛋白合成抑制水平相当。