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Updated: Feb 9, 2026

High-throughput Detection Method for Influenza Virus
Published on: February 4, 2012
miR-21-3p Regulates Influenza A Virus Replication by Targeting Histone Deacetylase-8
Binghui Xia1, Jiansheng Lu1, Rong Wang1
1Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Abstract:
Influenza A virus (IAV) is responsible for severe morbidity and mortality in animals and humans worldwide. miRNAs are a class of small noncoding single-stranded RNA molecules that can negatively regulate gene expression and play important roles in virus-host interaction. However, the roles of miRNAs in IAV infection are still not fully understood. Here, we profiled the cellular miRNAs of A549 cells infected with A/goose/Jilin/hb/2003 (H5N1) and a comparison A/Beijing/501/2009 (H1N1). miRNA microarray and quantitative PCR analysis showed that several miRNAs were differentially expressed in A549 cells during IAV infection. Subsequently, we demonstrated that IAV replication was essential for the regulation of these miRNAs, and bioinformatic analysis revealed that the targets of these miRNAs affected biological processes relevant to IAV replication. Specifically, miR-21-3p was found to be down-regulated in IAV-infected A549 cells and selected for further detailed analysis. Target prediction and functional study illustrated that miR-21-3p repressed the expression of HDAC8 by targeting its 3'UTR. Furthermore, we confirmed miR-21-3p could promote virus replication, which was similar to the result of knocking down HDAC8, indicating that miR-21-3p promoted IAV replication by suppressing HDAC8 expression. Altogether, our results suggest a potential host defense against IAV through down-regulation of miR-21-3p.
Insights
This study reveals that down-regulation of microRNA-21-3p (miR-21-3p) in influenza A virus (IAV) infection promotes viral replication by suppressing HDAC8. This suggests a host defense mechanism against IAV.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Influenza A virus (IAV) causes significant global morbidity and mortality.
- MicroRNAs (miRNAs) are key regulators of gene expression and crucial in virus-host interactions.
- The specific roles of miRNAs during IAV infection remain incompletely understood.
Purpose of the Study:
- To profile cellular miRNA expression in response to IAV infection.
- To elucidate the functional role of specific differentially expressed miRNAs in IAV replication.
- To identify the molecular mechanisms underlying miRNA-mediated regulation of IAV.
Main Methods:
- A549 cells were infected with H5N1 and H1N1 IAV strains.
- miRNA microarray and quantitative PCR were used for miRNA profiling.
- Bioinformatic analysis, target prediction, and functional assays were performed to validate miRNA targets and functions.
Main Results:
- IAV infection led to differential expression of several cellular miRNAs.
- miR-21-3p was significantly down-regulated in IAV-infected cells.
- miR-21-3p was found to repress HDAC8 expression, and its down-regulation promoted IAV replication.
Conclusions:
- Down-regulation of miR-21-3p promotes IAV replication by suppressing HDAC8.
- This suggests a potential host defense mechanism against IAV involving the down-regulation of miR-21-3p.
- The findings provide new insights into the complex interplay between host miRNAs and IAV.
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