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支原体病毒MVL51的复制。IV. 利福平对病毒合成的抑制作用。

Replication of mycoplasmavirus MVL51. IV. Inhibition of viral synthesis by rifampin.

作者信息

Das J, Maniloff J

出版信息

J Virol. 1976 Jun;18(3):969-76. doi: 10.1128/JVI.18.3.969-976.1976.

Abstract

The effect of rifampin on the replication of MVL51, a bullet-shaped mycoplasmavirus with single-stranded circular DNA of molecular weight 2 X 10(6), has been examined in a rifampin-resistant host cell. Rifampin does not block the early steps in MVL51 infection but does decrease the total amount of parental viral DNA taken up. The single-stranded parental viral DNA that enters the cell is found in membrane-associated, double-stranded DNA replicative forms I and II. Rifampin had no significant effect on the synthesis of progeny viral DNA RFI and RFII early in infection and SSI (single-stranded progeny viral chromosomes) later in infection. The rifampin block in virus synthesis was found to be in the step converting SSI into assembled virions. Rifampin was shown to affect the synthesis of virus-specific RNA, Which suggests that viral transcription is necessary for virion assembly.

摘要

利福平对MVL51复制的影响已在一株耐利福平的宿主细胞中进行了研究。MVL51是一种子弹状支原体病毒,具有分子量为2×10⁶的单链环状DNA。利福平并不阻断MVL51感染的早期步骤,但会减少摄取的亲代病毒DNA的总量。进入细胞的单链亲代病毒DNA存在于与膜相关的双链DNA复制形式I和II中。利福平在感染早期对子代病毒DNA RFI和RFII的合成以及感染后期对SSI(单链子代病毒染色体)的合成均无显著影响。发现利福平对病毒合成的阻断作用发生在将SSI转化为组装病毒体的步骤。研究表明利福平会影响病毒特异性RNA的合成,这表明病毒转录对于病毒体组装是必需的。

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