Honeysuckle-encoded atypical microRNA2911 directly targets influenza A viruses

Zhen Zhou(Nanjing University), Xihan Li(Nanjing University), Jinxiong Liu(Chinese Academy of Agricultural Sciences), Lei Dong(Nanjing University), Qun Chen(Nanjing University), Jialing Liu(Chinese Academy of Agricultural Sciences), Huihui Kong(Chinese Academy of Agricultural Sciences), Qianyi Zhang(Harbin Veterinary Research Institute), Xian Qi(Jiangsu Provincial Center for Disease Control and Prevention), Dongxia Hou(Nanjing University), Lin Zhang(Nanjing University), Guoquan Zhang(Chinese Academy of Agricultural Sciences), Yuchen Liu(Nanjing University), Yujing Zhang(Nanjing University), Jing Li(Nanjing University), Jin Wang(Nanjing University), Xi Chen(Nanjing University), Hua Wang(Jiangsu Provincial Center for Disease Control and Prevention), Junfeng Zhang(Nanjing University), Hualan Chen(Harbin Veterinary Research Institute), Ke Zen(Nanjing University), Chen‐Yu Zhang(Nanjing University)
Cell Research
October 7, 2014
Cited by 457Open Access
Full Text

Abstract

Influenza A viruses (IAVs), particularly H1N1, H5N1 and H7N9, pose a substantial threat to public health worldwide. Here, we report that MIR2911, a honeysuckle (HS)-encoded atypical microRNA, directly targets IAVs with a broad spectrum. MIR2911 is highly stable in HS decoction, and continuous drinking or gavage feeding of HS decoction leads to a significant elevation of the MIR2911 level in mouse peripheral blood and lung. Bioinformatics prediction and a luciferase reporter assay showed that MIR2911 could target various IAVs, including H1N1, H5N1 and H7N9. Synthetic MIR2911 significantly inhibited H1N1-encoded PB2 and NS1 protein expression, but did not affect mutants in which the MIR2911-binding nucleotide sequences were altered. Synthetic MIR2911, extracted RNA from HS decoction and HS decoction all significantly inhibited H1N1 viral replication and rescued viral infection-induced mouse weight loss, but did not affect infection with a mutant virus in which the MIR2911-binding nucleotide sequences of PB2 and NS1 were altered. Importantly, the inhibitory effect of HS decoction on viral replication was abolished by an anti-MIR2911 antagomir, indicating that the physiological concentration of MIR2911 in HS decoction could directly and sufficiently suppress H1N1 viral replication. MIR2911 also inhibited H5N1 and H7N9 viral replication in vitro and in vivo. Strikingly, administration of MIR2911 or HS decoction dramatically reduced mouse mortality caused by H5N1 infection. Our results demonstrate that MIR2911 is the first active component identified in Traditional Chinese Medicine to directly target various IAVs and may represent a novel type of natural product that effectively suppresses viral infection.


Related Papers

No related papers found

Powered by citation graph analysis