Infection and injury of human astrocytes by tick-borne encephalitis virus
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Astrocytes pathology physiology virology MeSH
- Cytokines genetics metabolism MeSH
- Endoplasmic Reticulum, Rough pathology MeSH
- Glial Fibrillary Acidic Protein biosynthesis MeSH
- Host-Pathogen Interactions MeSH
- Encephalitis, Tick-Borne etiology pathology physiopathology MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Matrix Metalloproteinase 9 biosynthesis MeSH
- Virus Replication MeSH
- Microscopy, Electron, Transmission MeSH
- Up-Regulation MeSH
- Encephalitis Viruses, Tick-Borne pathogenicity physiology MeSH
- Imaging, Three-Dimensional MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cytokines MeSH
- Glial Fibrillary Acidic Protein MeSH
- Matrix Metalloproteinase 9 MeSH
- MMP9 protein, human MeSH Browser
Tick-borne encephalitis (TBE), a disease caused by tick-borne encephalitis virus (TBEV), represents the most important flaviviral neural infection in Europe and north-eastern Asia. In the central nervous system (CNS), neurons are the primary target for TBEV infection; however, infection of non-neuronal CNS cells, such as astrocytes, is not well understood. In this study, we investigated the interaction between TBEV and primary human astrocytes. We report for the first time, to the best of our knowledge, that primary human astrocytes are sensitive to TBEV infection, although the infection did not affect their viability. The infection induced a marked increase in the expression of glial fibrillary acidic protein, a marker of astrocyte activation. In addition, expression of matrix metalloproteinase 9 and several key pro-inflammatory cytokines/chemokines (e.g. tumour necrosis factor α, interferon α, interleukin (IL)-1β, IL-6, IL-8, interferon γ-induced protein 10, macrophage inflammatory protein, but not monocyte chemotactic protein 1) was upregulated. Moreover, we present a detailed description of morphological changes in TBEV-infected cells, as investigated using three-dimensional electron tomography. Several novel ultrastructural changes were observed, including the formation of unique tubule-like structures of 17.9 ±0.15 nm diameter with associated viral particles and/or virus-induced vesicles and located in the rough endoplasmic reticulum of the TBEV-infected cells. This is the first demonstration that TBEV infection activates primary human astrocytes. The infected astrocytes might be a potential source of pro-inflammatory cytokines in the TBEV-infected brain, and might contribute to the TBEV-induced neurotoxicity and blood-brain barrier breakdown that occurs during TBE. The neuropathological significance of our observations is also discussed.
References provided by Crossref.org
Autoantibodies neutralizing type I IFNs underlie severe tick-borne encephalitis in ∼10% of patients
History of Arbovirus Research in the Czech Republic
Characterisation of Zika virus infection in primary human astrocytes
Electron Tomography Analysis of Tick-Borne Encephalitis Virus Infection in Human Neurons