Lemon S M, Hutt L M, Pagano J S
J Virol. 1978 Jan;25(1):138-45. doi: 10.1128/JVI.25.1.138-145.1978.
DNA synthesis in Epstein-Barr virus (EBV)-infected lymphocytes was inhibited by phosphonoacetic acid (PAA) as measured by [3H]thymidine incorporation. PAA, at a concentration of 200 microgram/ml, inhibited [3H]thymidine incorporation by human umbilical cord lymphocytes infected with EBV strain P94 but had little effect on DNA synthesis in mitogen-stimulated cells. Transformed cell lines did not develop from infected cord cell cultures treated with 100 microgram of PAA per ml. Cytofluorometric analysis showed marked increases in cellular nucleic acid content (RNA plus DNA) as early as 9 days after infection of cord cells in the absence of PAA and before significant enhancement of [3H]thymidine incorporation became apparent. Moreover, EBV led to increases in cellular nucleic acid even when 200 microgram of PAA per ml was added to cell cultures before infection. The apparent discrepancy between results obtained by [3H]thymidine incorporation and cytofluorometry is explained either by significant inhibition of cellular DNA polymerases by PAA or by a block at the G2 + M phase of the cell cycle. The data suggest that EBV initiates alterations in cellular nucleic acid synthesis or cell division without prior replication of viral DNA by virus-induced DNA polymerases.
通过[3H]胸苷掺入法测定,膦乙酸(PAA)可抑制爱泼斯坦-巴尔病毒(EBV)感染的淋巴细胞中的DNA合成。浓度为200微克/毫升的PAA可抑制感染EBV毒株P94的人脐带淋巴细胞的[3H]胸苷掺入,但对有丝分裂原刺激的细胞中的DNA合成影响很小。用每毫升100微克的PAA处理感染的脐带细胞培养物,未形成转化细胞系。细胞荧光分析显示,早在脐带细胞感染后9天,在PAA不存在且[3H]胸苷掺入显著增强之前,细胞核酸含量(RNA加DNA)就有明显增加。此外,即使在感染前向细胞培养物中加入每毫升200微克的PAA,EBV也会导致细胞核酸增加。通过[3H]胸苷掺入法和细胞荧光分析获得的结果之间的明显差异,要么是由于PAA对细胞DNA聚合酶的显著抑制,要么是由于细胞周期的G2+M期阻滞。数据表明,EBV在病毒诱导的DNA聚合酶未预先复制病毒DNA的情况下,启动细胞核酸合成或细胞分裂的改变。