Virology Journal (Jan 2020)

Identification of cellular microRNA miR-188-3p with broad-spectrum anti-influenza A virus activity

  • Huan Cui,
  • Chunmao Zhang,
  • Zongzheng Zhao,
  • Cheng Zhang,
  • Yingying Fu,
  • Jiaming Li,
  • Guanxi Chen,
  • Mengxi Lai,
  • Zhixiang Li,
  • Shishan Dong,
  • Ligong Chen,
  • Zhaoyang Li,
  • Chengyu Wang,
  • Juxiang Liu,
  • Yuwei Gao,
  • Zhendong Guo

DOI
https://doi.org/10.1186/s12985-020-1283-9
Journal volume & issue
Vol. 17, no. 1
pp. 1 – 12

Abstract

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Abstract Background Influenza A virus (IAV) continues to pose serious threats to public health. The current prophylaxis and therapeutic interventions for IAV requires frequent changes due to the continuous antigenic drift and antigenic shift of IAV. Emerging evidence indicates that the host microRNAs (miRNAs) play critical roles in intricate host-pathogen interaction networks. Cellular miRNAs may directly target virus to inhibit its infection and be developed as potential anti-virus drugs. Methods In this study, we established a broad-spectrum anti-IAV miRNA screening method using miRanda software. The screened miRNAs were further verified by luciferase assay, viral protein expression assay and virus replication assay. Results Five cellular miRNAs (miR-188-3p, miR-345-5p, miR-3183, miR-15-3p and miR-769-3p), targeting 99.96, 95.31, 92.9, 94.58 and 97.24% of human IAV strains recorded in NCBI, respectively, were chosen for further experimental verification. Finally, we found that miR-188-3p downregulated PB2 expression at both mRNA and protein levels by directly targeted the predicted sites on PB2 and effectively inhibited the replication of IAV (H1N1, H5N6 and H7N9) in A549 cells. Conclusions This is the first report screening cellular miRNAs that broad-spectrum inhibiting IAV infection. These findings suggested that cellular miR-188-3p could be used for RNAi-mediated anti-IAV therapeutic strategies.

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