Döhner Katinka, Serrero Manutea Christophe, Viejo-Borbolla Abel, Sodeik Beate
Department of Dermatology and Allergy, Hannover Medical School, Hannover, Germany.
RESIST Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Annu Rev Virol. 2024 Sep;11(1):215-238. doi: 10.1146/annurev-virology-100422-022751. Epub 2024 Aug 30.
The nucleoplasm, the cytosol, the inside of virions, and again the cytosol comprise the world in which the capsids of alphaherpesviruses encounter viral and host proteins that support or limit them in performing their tasks. Here, we review the fascinating conundrum of how specific protein-protein interactions late in alphaherpesvirus infection orchestrate capsid nuclear assembly, nuclear egress, and cytoplasmic envelopment, but target incoming capsids to the nuclear pores in naive cells to inject the viral genomes into the nucleoplasm for viral transcription and replication. Multiple capsid interactions with viral and host proteins have been characterized using viral mutants and assays that reconstitute key stages of the infection cycle. Keratinocytes, fibroblasts, mucosal epithelial cells, neurons, and immune cells employ cell type-specific intrinsic and cytokine-induced resistance mechanisms to restrict several stages of the viral infection cycle. However, concomitantly, alphaherpesviruses have evolved countermeasures to ensure efficient capsid function during infection.
核质、胞质溶胶、病毒粒子内部以及再次提及的胞质溶胶构成了一个世界,在这个世界中,α疱疹病毒的衣壳会遇到支持或限制它们执行任务的病毒蛋白和宿主蛋白。在此,我们回顾一个引人入胜的难题:α疱疹病毒感染后期特定的蛋白质 - 蛋白质相互作用如何协调衣壳的核组装、核输出和胞质包裹,但又将进入的衣壳靶向未感染细胞的核孔,以便将病毒基因组注入核质进行病毒转录和复制。利用病毒突变体和重建感染周期关键阶段的实验,已经对衣壳与病毒蛋白和宿主蛋白的多种相互作用进行了表征。角质形成细胞、成纤维细胞、黏膜上皮细胞、神经元和免疫细胞采用细胞类型特异性的固有和细胞因子诱导的抗性机制来限制病毒感染周期的多个阶段。然而,与此同时,α疱疹病毒也进化出了应对措施以确保感染期间衣壳的有效功能。