Why the study?
Coxsackievirus B5 can cause neurological complications and fatalities, but the functions of circular RNAs in response to infection remain unclear.
CV-B5 infection significantly alters circRNA expression profiles in SH-SY5Y cells, with specific circRNAs potentially regulating the host innate immune response to hamper viral replication.
CV-B5 infection alters circRNA profiles in neuronal cells; leaves open their role in modulating antiviral immunity.
Coxsackievirus B5 (CV-B5) is the causative agent of hand, foot and mouth disease (HFMD) that can cause neurological complications and fatalities. Circular RNA (circRNA) has been shown to play an important role in regulating pathogenic process. However, their functions of circRNA in response to CV-B5 infection remain unclear. In our research, RNA-seq was employed to analyze the expression profiles of circRNAs in SH-SY5Y cells with or without CV-B5 infection. Out of 5,665 circRNAs identified to be expressed in SH-SY5Y cells, 163 circRNAs were found to be differentially expressed significantly. Moreover, Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses showed that the differentially expressed circRNAs were mainly involved in ubiquitin-mediated proteolysis and signaling pathways during CV-B5 infection. Additionally, RT-qPCR was used to validate the RNA-seq data and a circRNA/miRNA/mRNA interaction network was constructed based on two circRNAs. Two circRNAs, such as: hsa_circ_0008378 and novel_circ_0014617, were associated with the regulation of innate immune response in host cells. Additionally, we confirmed the two circRANs up-regulated the key factors in the IFN signaling pathway, hampering viral replication. Our data provide a new perspective that facilitates further understanding on the virus-host mechanism.
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Li et al. (2022) studied this question.
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