Integrative RNA profiling of TBEV-infected neurons and astrocytes reveals potential pathogenic effectors

0559398 - BC 2023 RIV SE eng J - Článek v odborném periodiku
Selinger, Martin - Věchtová, P. - Tykalová, Hana - Oslejskova, P. - Rumlová, M. - Štěrba, J. - Grubhoffer, Libor
Integrative RNA profiling of TBEV-infected neurons and astrocytes reveals potential pathogenic effectors.
Computational and Structural Biotechnology Journal. Roč. 20, JUN (2022), s. 2759-2777. ISSN 2001-0370. E-ISSN 2001-0370
Grant CEP: GA MŠMT(CZ) LTARF18021; GA ČR(CZ) GA18-27204S
Institucionální podpora: RVO:60077344
Klíčová slova: Alternative splicing * Astrocytes * miRNA * Neurons * Response to infection * Neuropathogenesis * Tick-borne encephalitis virus * Transcriptomics
Obor OECD: Microbiology
Impakt faktor: 6, rok: 2022
Způsob publikování: Open access
https://www.sciencedirect.com/science/article/pii/S2001037022002070?via%3Dihub

Tick-borne encephalitis virus (TBEV), the most medically relevant tick-transmitted flavivirus in Eurasia, targets the host central nervous system and frequently causes severe encephalitis. The severity of TBEV-induced neuropathogenesis is highly cell-type specific and the exact mechanism responsible for such differences has not been fully described yet. Thus, we performed a comprehensive analysis of alterations in host poly-(A)/miRNA/lncRNA expression upon TBEV infection in vitro in human primary neurons (high cytopathic effect) and astrocytes (low cytopathic effect). Infection with severe but not mild TBEV strain resulted in a high neuronal death rate. In comparison, infection with either of TBEV strains in human astrocytes did not. Differential expression and splicing analyses with an in silico prediction of miRNA/mRNA/lncRNA/vd-sRNA networks found significant changes in inflammatory and immune response pathways, nervous system development and regulation of mitosis in TBEV Hypr-infected neurons. Candidate mechanisms responsible for the aforementioned phenomena include specific regulation of host mRNA levels via differentially expressed miRNAs/lncRNAs or vd-sRNAs mimicking endogenous miRNAs and virus-driven modulation of host pre-mRNA splicing. We suggest that these factors are responsible for the observed differences in the virulence manifestation of both TBEV strains in different cell lines. This work brings the first complex overview of alterations in the transcriptome of human astrocytes and neurons during the infection by two TBEV strains of different virulence. The resulting data could serve as a starting point for further studies dealing with the mechanism of TBEV-host interactions and the related processes of TBEV pathogenesis.(c) 2022 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
Trvalý link: https://hdl.handle.net/11104/0340284