Soft X-ray Tomography Reveals HSV-1-Induced Remodeling of Human B Cells.
Jian-Hua ChenBieke VanslembrouckAxel EkmanVesa AhoCarolyn A LarabellMark A Le GrosMaija Vihinen-RantaVenera WeinhardtPublished in: Viruses (2022)
Upon infection, viruses hijack the cell machinery and remodel host cell structures to utilize them for viral proliferation. Since viruses are about a thousand times smaller than their host cells, imaging virus-host interactions at high spatial resolution is like looking for a needle in a haystack. Scouting gross cellular changes with fluorescent microscopy is only possible for well-established viruses, where fluorescent tagging is developed. Soft X-ray tomography (SXT) offers 3D imaging of entire cells without the need for chemical fixation or labeling. Here, we use full-rotation SXT to visualize entire human B cells infected by the herpes simplex virus 1 (HSV-1). We have mapped the temporospatial remodeling of cells during the infection and observed changes in cellular structures, such as the presence of cytoplasmic stress granules and multivesicular structures, formation of nuclear virus-induced dense bodies, and aggregates of capsids. Our results demonstrate the power of SXT imaging for scouting virus-induced changes in infected cells and understanding the orchestration of virus-host remodeling quantitatively.
Keyphrases
- high resolution
- induced apoptosis
- cell cycle arrest
- herpes simplex virus
- endothelial cells
- signaling pathway
- endoplasmic reticulum stress
- single cell
- oxidative stress
- magnetic resonance imaging
- sars cov
- cell death
- quantum dots
- magnetic resonance
- computed tomography
- mesenchymal stem cells
- single molecule
- cell therapy
- high speed
- fluorescent probe