| Literature DB >> 30481615 |
Shu Pin Yu1, Kien Chai Ong2, David Perera3, Kum Thong Wong4.
Abstract
Japanese encephalitis virus (JEV) causes central nervous system neuronal injury and inflammation. A clear understanding of neuronal responses to JEV infection remains elusive. Using the Affymetrix array to investigate the transcriptome of infected SK-N-MC cells, 1316 and 2737 dysregulated genes (≥ 2/-2 fold change, P < 0.05) were found at 48 hours post-infection (hpi) and 60 hpi, respectively. The genes were mainly involved in anti-microbial responses, cell signalling, cellular function and maintenance, and cell death and survival. Among the most highly upregulated genes (≥ 10 folds, P < 0.05) were chemokines CCL5, CXCL11, IL8 and CXCL10. The upregulation and expression of CXCL11 were confirmed by qRT-PCR and immunofluorescence. Pathogen recognition receptors retinoic acid-inducible gene-1 (RIG-1) and melanoma differentiation-associated protein 5 (MDA5) were also upregulated. Our results strongly suggest that neuronal cells play a significant role in immunity against JEV. CXCL11, RIG-1 and MDA5 and other cytokines may be important in neuropathogenesis.Entities:
Keywords: CXCL11; Japanese encephalitis virus; MDA5; Neuronal infection; Proinflammatory mediators; RIG-1; RNA microarray; Transcriptome
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Year: 2018 PMID: 30481615 DOI: 10.1016/j.virol.2018.10.015
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616