Department of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
mSphere. 2018 Nov 21;3(6):e00599-18. doi: 10.1128/mSphereDirect.00599-18.
Cytopathic effects (CPEs) are a hallmark of infections. CPEs are difficult to observe due to phototoxicity from classical light microscopy. We report distinct patterns of virus infections in live cells using digital holo-tomographic microscopy (DHTM). DHTM is label-free and records the phase shift of low-energy light passing through the specimen on a transparent surface with minimal perturbation. DHTM measures the refractive index (RI) and computes the refractive index gradient (RIG), unveiling optical heterogeneity in cells. We find that vaccinia virus (VACV), herpes simplex virus (HSV), and rhinovirus (RV) infections progressively and distinctly increased RIG. VACV infection, but not HSV and RV infections, induced oscillations of cell volume, while all three viruses altered cytoplasmic membrane dynamics and induced apoptotic features akin to those caused by the chemical compound staurosporine. In sum, we introduce DHTM for quantitative label-free microscopy in infection research and uncover virus type-specific changes and CPE in living cells with minimal interference. This study introduces label-free digital holo-tomographic microscopy (DHTM) and refractive index gradient (RIG) measurements of live, virus-infected cells. We use DHTM to describe virus type-specific cytopathic effects, including cyclic volume changes of vaccinia virus infections, and cytoplasmic condensations in herpesvirus and rhinovirus infections, distinct from apoptotic cells. This work shows for the first time that DHTM is suitable to observe virus-infected cells and distinguishes virus type-specific signatures under noninvasive conditions. It provides a basis for future studies, where correlative fluorescence microscopy of cell and virus structures annotate distinct RIG values derived from DHTM.
细胞病变效应(CPE)是感染的一个标志。由于传统的光学显微镜的光毒性,CPE 很难观察到。我们使用数字全息断层显微镜(DHTM)报告了活细胞中病毒感染的不同模式。DHTM 是无标记的,它记录了低能量光通过透明表面的相位移动,对标本的干扰最小。DHTM 测量折射率(RI)并计算折射率梯度(RIG),揭示了细胞中的光学异质性。我们发现,牛痘病毒(VACV)、单纯疱疹病毒(HSV)和鼻病毒(RV)感染逐渐且明显地增加了 RIG。VACV 感染,但不是 HSV 和 RV 感染,引起了细胞体积的振荡,而这三种病毒都改变了细胞质膜的动力学,并诱导了类似于化学化合物 staurosporine 引起的凋亡特征。总之,我们引入了 DHTM 用于感染研究中的定量无标记显微镜,并在最小干扰的情况下揭示了活细胞中病毒类型特异性的变化和 CPE。本研究介绍了用于活细胞病毒感染的无标记数字全息断层显微镜(DHTM)和折射率梯度(RIG)测量。我们使用 DHTM 来描述病毒类型特异性的细胞病变效应,包括牛痘病毒感染的周期性体积变化,以及单纯疱疹病毒和鼻病毒感染中的细胞质凝聚,与凋亡细胞不同。这项工作首次表明,DHTM 适合观察病毒感染的细胞,并在非侵入性条件下区分病毒类型特异性的特征。它为未来的研究提供了基础,其中细胞和病毒结构的相关荧光显微镜注释了来自 DHTM 的不同的 RIG 值。