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Live Covisualization of Competing Adeno-Associated Virus and Herpes Simplex Virus Type 1 DNA Replication: Molecular Mechanisms of Interaction▿

机译:竞争性腺相关病毒和单纯疱疹病毒1型DNA复制的实时共可视化:相互作用的分子机制

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摘要

We performed live cell visualization assays to directly assess the interaction between competing adeno-associated virus (AAV) and herpes simplex virus type 1 (HSV-1) DNA replication. Our studies reveal the formation of separate AAV and HSV-1 replication compartments and the inhibition of HSV-1 replication compartment formation in the presence of AAV. AAV Rep is recruited into AAV replication compartments but not into those of HSV-1, while the single-stranded DNA-binding protein HSV-1 ICP8 is recruited into both AAV and HSV-1 replication compartments, although with differential staining patterns. Slot blot analysis of coinfected cells revealed a dose-dependent inhibition of HSV-1 DNA replication by wild-type AAV but not by rep-negative recombinant AAV. Consistent with this, Western blot analysis indicated that wild-type AAV affects the levels of the HSV-1 immediate-early protein ICP4 and the early protein ICP8 only modestly but strongly inhibits the accumulation of the late proteins VP16 and gC. Furthermore, we demonstrate that the presence of Rep in the absence of AAV DNA replication is sufficient for the inhibition of HSV-1. In particular, Rep68/78 proteins severely inhibit the formation of mature HSV-1 replication compartments and lead to the accumulation of ICP8 at sites of cellular DNA synthesis, a phenomenon previously observed in the presence of viral polymerase inhibitors. Taken together, our results suggest that AAV and HSV-1 replicate in separate compartments and that AAV Rep inhibits HSV-1 at the level of DNA replication.
机译:我们进行了活细胞可视化分析,以直接评估竞争性腺相关病毒(AAV)与单纯疱疹病毒1型(HSV-1)DNA复制之间的相互作用。我们的研究揭示了单独的AAV和HSV-1复制区室的形成以及在AAV存在下对HSV-1复制区室形成的抑制作用。 AAV Rep被募集到AAV复制区室中,但不募集到HSV-1的那些区中,而单链DNA结合蛋白HSV-1 ICP8被募集到AAV和HSV-1复制室中,尽管具有不同的染色模式。共感染细胞的狭缝印迹分析显示,野生型AAV抑制了HSV-1 DNA复制的剂量依赖性抑制作用,而rep阴性重组AAV则没有。与此相一致,蛋白质印迹分析表明野生型AAV仅适度影响HSV-1立即早期蛋白质ICP4和早期蛋白质ICP8的水平,但强烈抑制晚期蛋白质VP16和gC的积累。此外,我们证明了在没有AAV DNA复制的情况下Rep的存在足以抑制HSV-1。特别是,Rep68 / 78蛋白严重抑制了成熟的HSV-1复制区室的形成,并导致ICP8在细胞DNA合成位点的积累,这种现象是以前在病毒聚合酶抑制剂存在下观察到的。两者合计,我们的结果表明,AAV和HSV-1在不同的隔室中复制,并且AAV Rep在DNA复制水平上抑制HSV-1。

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