Institutes of Molecular Biology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
J Virol. 2012 Jun;86(12):6512-21. doi: 10.1128/JVI.00068-12. Epub 2012 Apr 4.
Herpesvirus nucleocapsids are translocated from their assembly site in the nucleus to the cytosol by acquisition of a primary envelope at the inner nuclear membrane which subsequently fuses with the outer nuclear membrane. This transport through the nuclear envelope requires homologs of the conserved herpesviral pUL31 and pUL34 proteins which form the nuclear egress complex (NEC). In its absence, 1,000-fold less virus progeny is produced. We isolated a UL34-negative mutant of the alphaherpesvirus pseudorabies virus (PrV), PrV-ΔUL34Pass, which regained replication competence after serial passages in cell culture by inducing nuclear envelope breakdown (NEBD) (B. G. Klupp, H. Granzow, and T. C. Mettenleiter, J. Virol. 85:8285-8292, 2011). To test whether this phenotype is unique, passaging experiments were repeated with a UL31 deletion mutant. After 60 passages, the resulting PrV-ΔUL31Pass replicated similarly to wild-type PrV. Ultrastructural analyses confirmed escape from the nucleus via NEBD, indicating an inherent genetic disposition in herpesviruses. To identify the mutated viral genes responsible for this phenotype, the genome of PrV-ΔUL34Pass was sequenced and compared to the genomes of parental PrV-Ka and PrV-ΔUL34. Targeted sequencing of PrV-ΔUL31Pass disclosed congruent mutations comprising genes encoding tegument proteins (pUL49, pUL46, pUL21, pUS2), envelope proteins (gI, pUS9), and protease pUL26. To investigate involvement of cellular pathways, different inhibitors of cellular kinases were tested. While induction of apoptosis or inhibition of caspases had no specific effect on the passaged mutants, roscovitine, a cyclin-dependent kinase inhibitor, and U0126, an inhibitor of MEK1/2, specifically impaired replication of the passaged mutants, indicating involvement of mitosis-related processes in herpesvirus-induced NEBD.
疱疹病毒核衣壳通过在内核膜上获得初级包膜从其组装部位易位到细胞质,随后该包膜与外核膜融合。这种穿过核膜的运输需要保守的疱疹病毒 pUL31 和 pUL34 蛋白的同源物,它们形成核外溢复合物 (NEC)。在没有它们的情况下,病毒产物的产量会减少 1000 倍。我们分离出了α疱疹病毒伪狂犬病病毒 (PrV) 的 UL34 缺失突变体 PrV-ΔUL34Pass,它在细胞培养中通过诱导核膜破裂 (NEBD) 连续传代后恢复了复制能力 (B. G. Klupp、H. Granzow 和 T. C. Mettenleiter,J. Virol. 85:8285-8292, 2011)。为了测试这种表型是否独特,我们用 UL31 缺失突变体重复了传代实验。经过 60 次传代,得到的 PrV-ΔUL31Pass 与野生型 PrV 的复制情况相似。超微结构分析证实了通过 NEBD 从细胞核逃逸,表明疱疹病毒具有内在的遗传倾向。为了确定导致这种表型的突变病毒基因,我们对 PrV-ΔUL34Pass 的基因组进行了测序,并与亲本 PrV-Ka 和 PrV-ΔUL34 的基因组进行了比较。对 PrV-ΔUL31Pass 的靶向测序揭示了包含编码包膜蛋白 (gI、pUS9) 和蛋白酶 pUL26 的基因的一致突变,以及编码衣壳蛋白 (pUL49、pUL46、pUL21、pUS2) 的基因。为了研究细胞途径的参与,我们测试了不同的细胞激酶抑制剂。虽然凋亡诱导或半胱天冬酶抑制对传代突变体没有特定影响,但细胞周期蛋白依赖性激酶抑制剂罗司维亭和 MEK1/2 抑制剂 U0126 特异性地损害了传代突变体的复制,表明有丝分裂相关过程参与了疱疹病毒诱导的 NEBD。