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Electron Tomography Analysis of Tick-Borne Encephalitis Virus Infection in Human Neurons
T. Bílý, M. Palus, L. Eyer, J. Elsterová, M. Vancová, D. Růžek,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
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PubMed
26073783
DOI
10.1038/srep10745
Knihovny.cz E-resources
- MeSH
- Autophagy drug effects genetics MeSH
- Benzylamines pharmacology MeSH
- Quinazolines pharmacology MeSH
- Endoplasmic Reticulum drug effects ultrastructure virology MeSH
- Humans MeSH
- Microtubules drug effects ultrastructure virology MeSH
- Cell Line, Tumor MeSH
- Neurons drug effects ultrastructure virology MeSH
- Nocodazole pharmacology MeSH
- Primary Cell Culture MeSH
- Virus Replication drug effects MeSH
- Sirolimus pharmacology MeSH
- Electron Microscope Tomography MeSH
- Virion drug effects growth & development ultrastructure MeSH
- Encephalitis Viruses, Tick-Borne drug effects growth & development ultrastructure MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Tick-borne encephalitis virus (TBEV) causes serious, potentially fatal neurological infections that affect humans in endemic regions of Europe and Asia. Neurons are the primary target for TBEV infection in the central nervous system. However, knowledge about this viral infection and virus-induced neuronal injury is fragmental. Here, we directly examined the pathology that occurs after TBEV infection in human primary neurons. We exploited the advantages of advanced high-pressure freezing and freeze-substitution techniques to achieve optimal preservation of infected cell architecture. Electron tomographic (ET) reconstructions elucidated high-resolution 3D images of the proliferating endoplasmic reticulum, and individual tubule-like structures of different diameters in the endoplasmic reticulum cisternae of single cells. ET revealed direct connections between the tubule-like structures and viral particles in the endoplasmic reticulum. Furthermore, ET showed connections between cellular microtubules and vacuoles that harbored the TBEV virions in neuronal extensions. This study was the first to characterize the 3D topographical organization of membranous whorls and autophagic vacuoles in TBEV-infected human neurons. The functional importance of autophagy during TBEV replication was studied in human neuroblastoma cells; stimulation of autophagy resulted in significantly increased dose-dependent TBEV production, whereas the inhibition of autophagy showed a profound, dose-dependent decrease of the yield of infectious virus.
References provided by Crossref.org
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