4.5 Article

Comprehensive analysis of the circRNA expression profile and circRNA-miRNA-mRNA network in the pathogenesis of EV-A71 infection

Journal

VIRUS RESEARCH
Volume 303, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.virusres.2021.198502

Keywords

Enterovirus A71 (EV-A71) infection; RNA sequencing (RNA-seq); Circular RNAs (circRNAs); Competing endogenous RNA (ceRNA); network1

Categories

Funding

  1. National Natural Sciences Foundations of China [32000128]
  2. Yunnan Applied Basic Research Projects [2019FB018, 2018ZF006]
  3. Fundamental Research Funds for the Central Universities
  4. PUMC Youth Fund [3332019004]
  5. Medical Reserve Talents of Yunnan Province Health and Family Planning [H-2017034, H-2019061]
  6. Doctoral Fund of the First People's Hospital of Yunnan Province [KHBS-2020-013]
  7. Top young talents of Yunnan province ten thousand talents plan

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In this study, RNA sequencing was used to characterize the expression of circRNAs during EV-A71 infection, identifying key circRNAs associated with the progression of viral infection.
Enterovirus A71 (EV-A71) is an important emerging virus posing a threat to children under five years old. Circular RNAs (circRNAs), a novel class of endogenous RNAs, have been recognized to play important roles in the onset and development of viral diseases. However, it has not been determined which specific circRNAs are involved in the pathological mechanisms of EV-A71 infection. In this study, RNA-sequencing (RNA-seq) was conducted to characterize differentially expressed circRNAs during the process of EV-A71 infection. Overall, 8726, 10405 and 4710 circRNAs were detected in the control, EV-A71-12 h and EV-A71-24 h groups, respectively, of which 1851 and 951 circRNAs were differentially expressed in the EV-A71-12 h and EV-A71-24 h groups versus the control group. The overlapping circRNAs in the EV-A71-infected groups were subjected to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis, which further demonstrated that the host genes of these circRNAs were principally implicated in activities associated with the progression of viral infection, such as immune system process, Wnt signaling pathway, etc. Additionally, qRTPCR detection showed that six selected circRNAs were identical to the sequencing data. To excavate the key circRNAs in EV-A71 infection, we comprehensively evaluated and integrated the relationship of circRNA/ miRNA/mRNA, and eventually screened 2 key circRNA regulatory axes, namely hsa_circ_0017115/hsa-miR-1505p/EGR1 and hsa_circ_0005060/hsa-miR-4685-5p/MMP2. In summary, our findings not only provide the first comprehensive expression and functional profile of circRNAs in response to EV-A71 infection, but also offer a novel direction to elucidate the molecular mechanism underlying viral pathogenesis and the cellular immune response in host-EV-A71 interactions.

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