Molenberghs Freya, Verschuuren Marlies, Barbier Michaël, Bogers Johannes J, Cools Nathalie, Delputte Peter, Schelhaas Mario, De Vos Winnok H
Laboratory of Cell Biology and Histology, Department of Veterinary Sciences and Health Sciences, University of Antwerp, Antwerp, Belgium.
Simply Complex Lab, UNAM, Bilkent University, Ankara, Turkey.
Cytometry A. 2022 Dec;101(12):1035-1048. doi: 10.1002/cyto.a.24663. Epub 2022 Jun 18.
Human papillomaviruses (HPV) are small, non-enveloped DNA viruses, which upon chronic infection can provoke cervical and head-and-neck cancers. Although the infectious life cycle of HPV has been studied and a vaccine is available for the most prevalent cancer-causing HPV types, there are no antiviral agents to treat infected patients. Hence, there is a need for novel therapeutic entry points and a means to identify them. In this work, we have used high-content microscopy to quantitatively investigate the early phase of HPV infection. Human cervical cancer cells and immortalized keratinocytes were exposed to pseudoviruses (PsV) of the widespread HPV type 16, in which the viral genome was replaced by a pseudogenome encoding a fluorescent reporter protein. Using the fluorescent signal as readout, we measured differences in infection between cell lines, which directly correlated with host cell proliferation rate. Parallel multiparametric analysis of nuclear organization revealed that HPV PsV infection alters nuclear organization and inflates promyelocytic leukemia protein body content, positioning these events at the early stage of HPV infection, upstream of viral replication. Time-resolved analysis revealed a marked heterogeneity in infection kinetics even between two daughter cells, which we attribute to differences in viral load. Consistent with the requirement for mitotic nuclear envelope breakdown, pharmacological inhibition of the cell cycle dramatically blunted infection efficiency. Thus, by systematic image-based single cell analysis, we revealed phenotypic alterations that accompany HPV PsV infection in individual cells, and which may be relevant for therapeutic drug screens.
人乳头瘤病毒(HPV)是小型无包膜DNA病毒,长期感染可引发宫颈癌和头颈癌。尽管人们已经对HPV的感染生命周期进行了研究,并且针对最常见的致癌HPV类型已有疫苗,但目前尚无抗病毒药物可用于治疗受感染患者。因此,需要新的治疗切入点以及识别这些切入点的方法。在这项研究中,我们使用高内涵显微镜技术对HPV感染的早期阶段进行了定量研究。将人宫颈癌细胞和永生化角质形成细胞暴露于广泛流行的HPV 16型假病毒(PsV)中,该病毒的基因组被编码荧光报告蛋白的假基因组所取代。以荧光信号作为读数,我们测量了细胞系之间感染的差异,这与宿主细胞增殖率直接相关。对核组织的平行多参数分析表明,HPV PsV感染会改变核组织并增加早幼粒细胞白血病蛋白体的含量,这些事件发生在HPV感染的早期,即病毒复制的上游。时间分辨分析显示,即使在两个子细胞之间,感染动力学也存在显著异质性,我们将其归因于病毒载量的差异。与有丝分裂核膜破裂的要求一致,细胞周期的药理学抑制作用显著降低了感染效率。因此,通过基于图像的系统单细胞分析,我们揭示了单个细胞中伴随HPV PsV感染的表型改变,这些改变可能与治疗药物筛选相关。